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Latest revision as of 03:52, 27 October 2012

UNAM-Genomics_Mexico

Arabinose/Xylose AND Gate Notebook

2 JUNE

2.1 06/07/12
2.2 06/12/12
2.3 06/13/12
2.4 06/14/12
2.5 06/15/12
2.6 06/18/12
2.7 06/19/12
2.8 06/22/12
2.9 06/25/12
2.10 06/26/12
2.11 06/27/12
2.12 06/29/12

3 JULY

3.1 07/03/12
3.2 07/04/12
3.3 07/06/12
3.4 07/07/12
3.5 07/08/12
3.6 07/09/12
3.7 07/10/12
3.8 07/11/12
3.9 07/12/12
3.10 07/13/12
3.11 07/14/12
3.12 07/16/12
3.13 07/17/12
3.14 07/18/12
3.15 07/19/12
3.16 07/20/12
3.17 07/23/12
3.18 07/24/12
3.19 07/25/12
3.20 07/26/12
3.21 07/27/12
3.22 07/30/12
3.23 07/31/12

4 AUGUST

4.1 08/01/12
4.2 08/02/12
4.3 08/03/12
4.4 08/06/12
4.5 08/08/12
4.6 08/09/12
4.7 08/10/12
4.8 08/13/12
4.9 08/16/12
4.10 08/20/12
4.11 08/21/12
4.12 08/22/12
4.13 08/23/12
4.14 08/24/12
4.15 08/25/12
4.16 08/28/12
4.17 08/29/12
4.18 08/30/12
4.19 08/31/12

5 SEPTEMBER

5.1 09/01/12
5.2 09/03/12
5.3 09/04/12
5.4 09/05/12
5.5 09/06/12
5.6 09/14/12
5.7 09/16/12
5.8 09/17/12
5.9 09/18/12
5.10 09/19/12
5.11 09/19/12
5.12 09/20/12
5.13 09/21/12
5.14 09/22/12
5.15 09/23/12
5.16 09/24/12
5.17 09/26/12
5.18 09/27/12

OCTOBER
5.19 10/09/12
5.20 10/10/12
5.21 10/11/12
5.22 10/12/12
5.23 10/13/12

On hover the images to see descriptions

JUNE

1. 1 kb ladder
2.E1010

06/07/12

PY BROTH 10g salt/L
PSB2K3 kanamicin
We transformed RFP E1010.
plate 1 18F
plate 2 17E
Stock 50 mg/mL
E.coli 1/1000
TRANSFORMATION PROTOCOL.
We made liquid cultures with colonies LIQUID CULTURE.
We extracted plasmids PLASMID EXTRACTION PROTOCOL.
We ran a gel to check the extraction GEL ELECTROPHORESIS PROTOCOL.

06/12/12

We made glycerols of the bacteria
GLYCEROL PROTOCOL .
We transformed plasmid pHp45 TRANSFORMATION PROTOCOL.

1. 1 kb ladder
2.E1010

06/13/12

We ran gel and extracted from gel LIQUID CULTURE.
We made liquid cultures LIQUID CULTURE and lysed.

1. 1 kb ladder
We extracted from gel

06/14/12

We extracted from gel LIQUID CULTURE.
We made glycerols of pHp45 Ω GLYCEROL PROTOCOL .
We transformed PSB2K3 Km (Kanamycin) 5C BBa_J04450 PSB4A5 Am (ampicillin) 1I BBa_J04450 AraC BBa_C0080
2012 14L plate 1 pSB2K3 Km+
2011 14L plate 1 pSB2K3 Km+
2012 14L plate 1 pSB2K3 Km+
TRANSFORMATION PROTOCOL.

1. 1 kb ladder
pHp45 Ω with E/P
We extracted from gel

06/15/12

> Digested pHp45 Ω with E/P LIQUID CULTURE.
> We extracted plasmid with kit.
> Ran a gel GEL ELECTROPHORESIS PROTOCOL . (5)
>Extracted from gel LIQUID CULTURE.

ARAC
>From the overnight plate we prepared liquid culture LIQUID CULTURE.
>We left them incubating overnight.
>We left a plate (LB Km DH5α C0080 and a control).

06/18/12

>Plasmid extraction AraC with kit.
>C0080-psB2K3 915 bp
>Streaked 4 LB Km 30 plates DH5α psB2K3.
>It seemed as though there were two different colonies (white) and there had been a mutation. Normally they are red.
>Ran gel with Spr/Strr (eppendorf -20ºC) GEL ELECTROPHORESIS PROTOCOL.
>Made glycerols from one tube of DH5α C0080 Km 50 -> 04.
>Made glycerols from one tube of DH5α PSB4A5 Amp 100 -> 05 GLYCEROL PROTOCOL.
>Digested C0080 X,S.
>Digested B0014 E,P LIQUID CULTURE.

1. 1 kb ladder
Digested B0014 with E, P and with E,X

06/19/12

>Digested B0014 with E, P and with E,X. LIQUID CULTURE.
>Ran gels with yesterday’s digestions GEL ELECTROPHORESIS PROTOCOL .
2 B0014 E,X and 3 B0014 E,P were discarded because of problems in the preparation.
C0080 is in the first lane.
>Extracted from gel C0080 X,S LIQUID CULTURE.
>Made glycerols from 4 plates LB Km DH5α pSB2K3 GLYCEROL PROTOCOL .
>Take out AmyE 5’ from distribution [DNA KIT PLATE INSTRUCTIONS].
AmyE 5’ 18K plate 3 2010, 2011, 2012
AmyE 3’ 18M plate 3 2010, 2011, 2012
>Digested B0014 with E,X and E,P again LIQUID CULTURE.

06/22/12

>Ran gels with digestions B0014 with E,X and E,P GEL ELECTROPHORESIS PROTOCOL.

>Dephosphated B0014 E,X and B0014 E,P.

06/25/12

>Took LasR BBa_B0079 plate 1 2010,2011,2012 psB1A2 Amp+ from distribution [DNA KIT PLATE INSTRUCTIONS].

06/26/12

>Ran gel with psB2K3 and psB4A5 GEL ELECTROPHORESIS PROTOCOL .

06/27/12

>Transformed with plasmid B0079 1576 bp psB1A2 12A TRANSFORMATION PROTOCOL.
LasR B0079 plasmid Amp+ 12A plate 1 2010,2011
AmyE 5’ BBa_K143001 Km+ 18K plate 3 2010 and 16M, 18K 2011
AmyE 3’ BBa_K143002 Km+ 18M plate 3 2010 and 16O, 18M 2011
AmyE 5’ grew 2 colonies.

06/29/12

>We did a DH5α K143001 Km30 Amp 100 glycerol GLYCEROL PROTOCOL 07.
>We plated twice DH5α K143002 Km 30 Amp 100 + control and twice DH5α B0079 Amp 100 + control
These were both plated in 2 plates each.
They were left overnight since they had not grown by 7:00 pm so the next day glycerols were made.
>Liquid cultures LIQUID CULTURE.

2 tubes DH5α K143001 Km30 Amp 100
2 tubes DH5α K143002 Km30 Amp 100
2 tubes DH5α B0079 Amp 100
1 tube LB Km 30 Amp 100 control
1 tube LB Amp 100 control
>From the 6 tubes we extracted plasmid from kit.

JULY

07/02/12
>Digestions LIQUID CULTURE.
B0079 digestion with S,P
K143001 with S,P
K143002 with S,P
>PCR’s
•AraC
•Cassete ΩSpr/Strr
PCR PROTOCOL

After Cassete ΩSpr/Strr PCR we ran a gel

B0079 digestion with S,P
K143001 with S,P
K143002 with S,P

07/03/12

>After Cassete ΩSpr/Strr PCR we ran a gel GEL ELECTROPHORESIS PROTOCOL . (8)
>Ran gel with digestions from yesterday. (9)
>Did band extractions LIQUID CULTURE.
>Stored at -20ºC.
>Did PCR to Cassete ΩSpr/Strr to add RBS and prefix/suffix.
>Left digesting with E,S LIQUID CULTURE.

We dephosphated B0079 S,P, K143001 S,P, K143002 E,X

07/04/12

>We dephosphated B0079 S,P, K143001 S,P, K143002 E,X (9.1).
>Ligated Cassete ΩSpr/Strr +K143002 dephosphated(digested with E,X and E,S).
>Transformed ligation and left overnight plated TRANSFORMATION PROTOCOL.
>Extracted plasmid PBBR1 GusA in 2 1.5 mL eppendorfs.
>Digested with PstI LIQUID CULTURE.

07/06/12

4 LB Km30 Spec60 DH5α ΩSpr/Strr +K143002 still have not grown.
Ran a gel with yesterday’s digestions to chek if they were done properly (10)
GEL ELECTROPHORESIS PROTOCOL .
Ran another gel with the rest of the samples.
Extracted GusA fragment
LIQUID CULTURE.
Repeated ligation ΩSpr/Strr +K143002 E,X dephosphated LIGATION PROTOCOL.
Repeated ΩSpr/Strr PCR.

07/07/12

Transformed DH5α ΩSpr/Strr +K143002 ligation LIGATION PROTOCOL.
Plated LB Km30 Spec 60 DH5α ΩSpr/Strr +K143002 .

07/08/12

Transformed DH5α ΩSpr/Strr +K143002 ligation LIGATION PROTOCOL.
Plated LB Km30 Spec 60 DH5α ΩSpr/Strr +K143002.

We dephosphated B0079 S,P, K143001 S,P, K143002 E,X

1 PCR omega P
2 PCR omega I
3 PCR AraC P
4 PCR AraC I
5 ladder 1 Kb

07/09/12

From yesterday’s transformations only one colony grew.
From the previous transformation only 2 colonies grew.
These 3 were streaked in 3 plates:
DH5α ΩSpr/Strr +K143002 LB Km 30 Sp 100 1.
DH5α ΩSpr/Strr +K143002 LB Km 30 Sp 100 2.
DH5α ΩSpr/Strr +K143002 LB Km 30 Sp 100 3.
LB Km 30 Sp 100 control.
Did liquid cultures in 3 tubes:
ΩSpr/Strr +K143002 LB Km 30 Sp 100 1.
ΩSpr/Strr +K143002 LB Km 30 Sp 100 2.
ΩSpr/Strr +K143002 LB Km 30 Sp 100 3.
LB Km30 Sp 100 control.
LIQUID CULTURE.

Ran a gel with: (11)
GusA P
PBBR1 GusA
Ω E PCR P
Ω PCR P
Ω PCR I
Ω E
Ω PCR I
GEL ELECTROPHORESIS PROTOCOL
Did GusA primers dissolution for PCR.
GusA PCR
Gel Extraction by kit of lanes 3 and 5 LIQUID CULTURE.

PCR omega P, PCR omega I, PCR AraC P, PCR AraC I
Add 10 μl of each primer (LW and UP).
Add 3 μl of plasmid (P).
Add 30.4 μl buffer.
Add 5 μl Mg.
Add 8 μl DNTp’s.
Add 42.6μl H2O miliQ.
Add 1 μl RTTG polymerase.
Centrifuge (spin) 8 secs.
Add vegetable oil till the eppendorf is full.
Place eppendorf 1 mL in thermocycler.
Run PCR with program “BERNA”.

GusA digestions with X,P; Ω+AmyE 3’ with E,X; AraC PCR with E,S

07/10/12

•GusA digestions with X,P; Ω+AmyE 3’ with E,X; AraC PCR with E,S (2 times) DIGESTIONS. (11.2)

07/11/12

•GusA PCR digestions with E,S; Ω+AmyE 3’ with E,X LIQUID CULTURE.
•T.V. AraC PCR+ Ω+AmyE 3’ E,X dephosphated ligation LIGATION PROTOCOL.

1. ladder.
2. GusA PCR E,S.
3. Ω+AmyE 3’ with E,X.

07/12/12

•Ran a gel with yesterday’s digestions: (12)

GEL ELECTROPHORESIS PROTOCOL .

•Transformed AraC PCR+ Ω+AmyE 3’ ligation in two tubes TRANSFORMATION PROTOCOL.

•From pfrc54 liquid cultures (A3) that were grown overnight we extracted plasmid.
•Made glycerols from 2 LB Km 30 Sp100 DH5α Ω+AmyE 3’ plates and from 1 LB Amp100 pfrc54 (A3) plates with control GLYCEROL PROTOCOL .
•Ligated GusA PCR with B0014 E,X desphophorylated LIGATION PROTOCOL.

•Digested Pfrc54 (A3) with S,P LIQUID CULTURE.

•Desphophorylated Ω+AmyE 3’ E,X.

•Ran gel with pfrc54 S,P

07/13/12

•Ran gel with pfrc54 S,P GEL ELECTROPHORESIS PROTOCOL . (13)
•Transformation of GusA PCR + B0014 ligation TRANSFORMATION PROTOCOL.
•Transformed with GFP E0040 psBIA2.
•Liquid Cultures with ligation: AraC+ Ω+AmyE 3’ for plasmid extraction at night TRANSFORMATION PROTOCOL.
•B. Subtitils competent cells.

07/14/12

•From 24 AraC+ Ω+AmyE 3’ LB Km 30 Sp 100 DH5α tubes:
•Extracted pellets
•Extracted plasmids.
•Ran gel GEL ELECTROPHORESIS PROTOCOL .

•From transformed DH5α km 30:
GusA+B0014 DH5α Km50 24 pellets
E0040 DH5α LB Amp100
From these two we:
•Did liquid cultures LIQUID CULTURE.
•Extracted plasmid.
•From the GusA+E0014 transformation we took 24 colonies, did liquid cultures and extracted plasmid LIQUID CULTURE.
•Ran gel with this transformation GEL ELECTROPHORESIS PROTOCOL .

07/16/12

•Digested E,P AraC+ Ω+AmyE 3’
•Ω+AmyE 3’ E,P LIQUID CULTURE.

Digested E,P AraC+ Ω+AmyE 3’
Ω+AmyE 3’ E,P

07/17/12

•Ran gel with yesterday’s digestions LIQUID CULTURE. (14)
•The gel we ran didn’t work, probably because the agarose was not prepared correctly.
•Digested 12, 15, 18, 21 with AraC+ Ω+AmyE 3 with E and also with P’; B0014 with E,X; E0040 with X,S LIQUID CULTURE.

•Digested 12, 15, 18, 21 with AraC+ Ω+AmyE 3 with E and also with P’; B0014 with E,X; E0040 with X,S

07/18/12

•From yesterday’s digestions we ran a gel GEL ELECTROPHORESIS PROTOCOL . (15)

•We made liquid cultures of AraC+ Ω+AmyE 3’ 12, 15, 21 LIQUID CULTURE.

•We ligated AraC PCR E,S dephosphated with + Ω+AmyE 3’ LIGATION PROTOCOL.

•We digested 1 + Ω+AmyE 3’ E,P LIQUID CULTURE.

07/19/12

•We ran We digested 1 + Ω+AmyE 3’ E,P with Miguel’s enzymes and with Abiel’s enzymes LIQUID CULTURE.

•We transformed with ligations AraC+ Ω+AmyE 3’ E and + Ω+AmyE 3’ E TRANSFORMATION PROTOCOL.

•Extracted plasmids from AraC+ Ω+AmyE 3’ 12,15,21.

•Digested E0040 X,S 2,3,4,5,6; ligations AraC+ Ω+AmyE 3’ E 12,15,21; ligations AraC+ Ω+AmyE 3’ P LIQUID CULTURE.

Digested E0040 X,S 2,3,4,5,6; ligations AraC+ Ω+AmyE 3’ E 12,15,21; ligations AraC+ Ω+AmyE 3’ P

07/20/12

•Ran gel with yesterday’s digestions GEL ELECTROPHORESIS PROTOCOL . (16)
•Transformed GusA+B0014 in two tubes TRANSFORMATION PROTOCOL.
•Made liquid cultures from AraC+ Ω+AmyE 3’s transformation LB Km30 Sp 100 and control LB Km 30 Sp100 LIQUID CULTURE.

07/23/12

•From 24 GusA+B0014 tubes (-) we didn’t do anything.
•From 4 AraC+ Ω+AmyE 3’ we extracted plasmid.
•Digested from the 4 AraC+ Ω+AmyE 3’ E,X; X; P and GusA PCR with X,P LIQUID CULTURE.

07/24/12

•Digested B0014 E with X B0014 X with E
•Digested AraC+ Ω+AmyE 3’ 1,2,3,4 with E,P LIQUID CULTURE.

07/25/12

•Ran gel of digested AraC+ Ω+AmyE 3’ 1,2,3,4 with E,P LIQUID CULTURE.
•Joined B0014 E with X B0014 X with E digestions.
•Made liquid cultures from 2 days old plated GusA+B0014 and extracted plasmid LIQUID CULTURE. Transformed TRANSFORMATION PROTOCOL.
•From LasR DH5α make liquid cultures and plate LIQUID CULTURE.
•Digested Ω+AmyE 3’ with X,P; E,S; C0080 X,P; E,S; S,P LIQUID CULTURE.
•Ligated Gus PCR X,P with B0079 S,P dephosphorylated LIGATION PROTOCOL.

1.Ω+AmyE 3’ X,P
2. Ω+AmyE 3’ E,S
3.C0080 X,P
4.C0080 E,S
5.C0080 S,P
6.ladder

07/26/12

•From C0179 (LasR) transformation which grew colonies, we made two liquid cultures: DH5α C0179 LB Cb 100 (two cultures) and a control without bacteria LIQUID CULTURE.

•We extracted plasmid from 8 C0179 tubes, from 2 tubes of C0179 (Miguel’s transformation), Puc, B.S. control and PSB4AE.

•Due to problems with the way we did the transformations of ligations we repeated them:
GusAPCR X,P+ B0079 S,P dephosphorylated

GusAPCR X,P+ B0079 S,P dephosphorylated (-)

GusAPCR X,P+ A3 S,P dephosphorylated

GusAPCR X,P+ A3 S,P dephosphorylated (-)
TRANSFORMATION PROTOCOL.

•Did the following digestions LIQUID CULTURE.
•AraC+ Ω+AmyE 3’ S,P 1,2,3,4
•K143002 X,P
•AraC+ Ω S,P
•C0179 X,S

07/27/12

Ligated AraC+ Ω S,P dephosphorylated + K143002 X,P LIGATION PROTOCOL.

07/30/12

•Transformed with ligations:
•AraC+ Ω dephosphprylated +K143002 X,P
•GusAPCR X,P+ A3 S,P dephosphorylated
•GusAPCR X,P+ B0079 S,P dephosphorylated
•Transformed the following sythesis:
•91996 Pveg 140 bp
•91997 ArsR-CzrA_promoter 1 194 bp
•91998 ArsR-CzrA_promoter 2 221 bp
•91999 ArsR-CzrA_promoter 3 213 bp
•92000 pBad-pXyl 387 bp
•92001 XylR 1117pb
•92002 CI_pro_(NAND_INHIBITOR) 774
•These synthesis come in pJ209 and supposedly come with Chloramphenicol+ and Gentamicin+ resistance, but we discovered that only Chloramphenicol worked. TRANSFORMATION PROTOCOL.

•Make liquid cultures of the following transformations for tomorrow LIQUID CULTURE:
•AraC+ Ω+K143002
•GusA+A3
•GusA+B0079
•Synthesis

07/31/12

Extracted plasmids from yesterday’s cultures and from K143002 cultures that were in the other lab.

AUGUST

08/01/12

Digested XylR 01 X,P; pBAD-pXyl X,P; Pveg 96 S,P LIQUID CULTURE.

1 PCR GusA I
2 PCR GusA I
3 PCR GusA P
4 PCR GusA P
5 ladder 1 Kb

08/02/12

•Extracted plasmids from liquid cultures:
AraC+ Ω+K143002
•GusA+A3
•GusA+BBR1

PCR GusA, GusA I, PCR GusA P, PCR GusA I

•Add 10 μl of each primer (LW and UP).
•Add 3 μl of plasmid (P).
•Add 30.4 μl buffer.
•Add 5 μl Mg.
•Add 8 μl DNTp’s.
•Add 42.6μl H2O miliQ.
•Add 1 μl RTTG polymerase.
•Centrifuge (spin) 8 secs.
•Add mineral oil till the eppendorf is full.
•Place eppendorf 1 mL in thermocycler.
•Run PCR with program “BERNA”.

1.GusA PCR 1
2.GusA PCR 2
3.A3+GusA 1
4.A3+GusA 2
5.A3+GusA 3
6.P GusA
7.P GusA 2
8.Ladder
9.01
10.06
11.96

08/03/12

• Ran a gel with: (18)

GEL ELECTROPHORESIS PROTOCOL .
•Ran another gel to extract with:
1.GusA PCR 1
2.GusA PCR 2
3.00
4.01
GEL ELECTROPHORESIS PROTOCOL .
•Did the following digestions LIQUID CULTURE:

• Ω+K143002 E,X; A3+GusA E,S; GusAPCR X,P

•Extracted GusAPCR X,P digestion LIQUID CULTURE.

•Left the following ligation: AraC+ Ω+K143002 LIGATION PROTOCOL.

1.A3+GusA 2
2.A3+GusA 3
3. Ω+AmyE 3’ 2
4. Ω+AmyE 3’ 3
5.XylR X,P
6.pBad-pXyl X,P
7.GusA PCR X,P

08/06/12

•Made liquid cultures of Ω+K143002 (2 cultures+1 control) and AraC+ Ω+K143002 (2 cultures+1 control) LIQUID CULTURE.
•Ligated GusAPCR X,P+B0079 S,P dephosphorylated LIGATION PROTOCOL.
•Ran a Gel with: (19)

Digested 14 tubes of AraC+ Ω+AmyE 3’ E,P

08/08/12

BBa_B0040 6I psB1A2 Amp+ plate 1
Digested 14 tubes of AraC+ Ω+AmyE 3’ E,P LIQUID CULTURE. (19.1)

08/09/12

•From yesterday’s PCR’s :
• E0040 plasmid 1
E0040 plasmid 2
E0040 digested 1
E0040 digested 2
We purified with PCR kit

•Ran a gel GEL ELECTROPHORESIS PROTOCOL .
•Made 14 PCR’s from AraC+ Ω+AmyE 3’.
•From B0079+GusA ligation and B0040 transformation: •Grew colonies.
•Made liquid cultures LIQUID CULTURE.
•Streaked these in a new plate.
•Diluted plasmid E0080 2 1/50.

08/10/12

•Yesterday’s gel did not come out as expected so we repeated the PCR.

1.AraC+ Ω+AmyE 3’
2-14.AraC+ Ω+AmyE 3’
15.AraC+ Ω 1
16.AraC+ Ω 1
17.AraC+ Ω 1
18.PCR 1 GFP
19.PCR GFP

08/13/12

•After running a gel with 14 PCR’s AraC+ Ω+AmyE 3’ and it did not come out as expected, we ran a gel with the ligation AraC+ Ω+AmyE 3’ to select candidate (that weight the same as the ligation) GEL ELECTROPHORESIS PROTOCOL : (20)

•Extracted pasmids form liquid cultures: B0049, B0079+GusA.

•AraC+ Ω+AmyE 3’ undigested didn’t run in the gel as expected, it ran similarly to AraC+ Ω

• We repeated the ligation AraC+ Ω S,P dephosphorylated+K143002 X,P LIGATION PROTOCOL.

• GFP PCR gel came out with two bands one is GFP and the other one are the primers, even after purifying by kit. We joined 2 GFP PCR tubes.

• We ran a gel to extract.

1.6 AraC+ Ω+AmyE 3’ E with P.

2.8 AraC+ Ω+AmyE 3’ E with P.
3.11 AraC+ Ω+AmyE 3’ E with P.
4.12 AraC+ Ω+AmyE 3’ E with P.
5.6 AraC+ Ω+AmyE 3’ with E,X.
6.8 AraC+ Ω+AmyE 3’ with E,X.
7.11 AraC+ Ω+AmyE 3’ with E,X.
8.12 AraC+ Ω+AmyE 3’ with E,X.
9.00 pBad/pXyl with S,P.
10.Ladder.
11.E0040 PCR E,S to extract the correct band.

08/16/12

•Ran a gel with yesterday’s digestions:

•Digested:
ArSR-CzrA 97 with S,P
ArSR-CzrA 98 with S,P
ArSR-CzrA 99 with S,P
E0040 PCR with E,S
Digestion Protocol.

08/20/12

•Ligated B0079 S,P dephosphorylated + GusA PCR X,P and pVeg S,P dephosphorylated + XylR X,P LIGATION PROTOCOL.

08/21/12

•Joined both .6 ml tubes of B0014 EX and B0014 XE in one and dephosphorylated.
•Extracted plasmid from the 24 tubes of of ligation K143001+pBad/pXylR.
•Digested Ω+AmyE 3’ with E,X and + Ω+AmyE 3’ II with E,X (obtained these two from glycerols stored at -80ºC LIQUID CULTURE.

Digested K143001+PBad, pXyl with E,S

1.K143001+PBad, pXyl E,S 10
2.K143001+PBad, pXyl E,S 11
3.K143001+PBad, pXyl E,S 12
4.A3 PCR
5.A3 PCR
6.E0040 PCR E,S
7.B0014 E,X dephosphorylated
8. Ω+AmyE 3’ E,X
9. Ω+AmyE 3’ E,X II
10.Ladder

08/22/12

•We did 2 PCR’s for A3.

•Digested K143001+PBad, pXyl with E,S
LIQUID CULTURE. (22.1)

GEL ELECTROPHORESIS PROTOCOL .
•Did band extraction of:
1. K143001+PBad, pXyl E,S 10
2.K143001+PBad, pXyl E,S 11
3.K143001+PBad, pXyl E,S 12

LIQUID CULTURE.
•Made liquid cultures from E1010+Boo14 that the other lab gave us and did 2 plates for glycerol Km+ LIQUID CULTURE
GLYCEROL PROTOCOL .

•Did 2 plates for glycerol of both K143001+pBad/pXyl 10y11 Km+ and AraC+ Ω+AmyE 3’ 6,8,11,12 Km+ and Spectinomycin+ GLYCEROL PROTOCOL .

•Transformed ligations:
B0079+GusA Amp+
Pveg+XylR Chloramphenicol+ TRANSFORMATION PROTOCOL..

1. Ω+AmyE 3’ E,X 6.2
2.Ω+AmyE 3’ II E,X
3.97 ArsR-CzrA
4.98 ArsR-CzrA
5.99 ArsR-CzrA

08/23/12

•The negative controls were contaminated. We didn’t manipulate the ones that had grown because of this.
•Ran gel with GEL ELECTROPHORESIS PROTOCOL : (23.01)
Digestion Protocol.

08/24/12

From plate with ligation E0040+B0014, ligation K143001+pBad,pXyl 10 and 11, and ligation AraC+ Ω+AmyE 3’ 6 and 8 we streaked 2 plates for glycerol of each ligation.
Repeated ligation B0079+GusA.

Ligated E0040 PCR E,S+B0014 E,X dephospohylated LIGATION PROTOCOL.

Made 2 new plates from Pveg+XylR ligation and liquid cultures LIQUID CULTURE.

08/25/12

Extracted pellet from 16 tubes of pVeg+XylR that were left overnight.

Ligated B0079+GusA and B0040+B0014 LIGATION PROTOCOL.

08/28/12

Made liquid cultures from transformations tht were left overnight -R0079+GusA
-R0079+GusA (-)
-E0040+B0014
-E0040+B0014 (-)
LIQUID CULTURE.

1. A3 PCR 1.
2. A3 PCR 2.
3. Ω+AmyE 3’ S,P *.
4. Ω+AmyE 3’ S,P .
5. Pveg+XylR E,S 2.
6. Pveg+XylR E,S 3.
7. Pveg+XylR E,S 4.

08/29/12

Digested Pveg+XylR 2,3,4 with E,S.

Digested Ω+AmyE 3’ with S,P DIGESTION.

Ran a PCR with A3 PCR (2 .6 ml tubes).

Ran a gel with
GEL ELECTROPHORESIS PROTOCOL : (23.01)

1-23. E0040 + B0014 colonies
24-29. B0079+GusA 1
30. B0079

08/30/12

•Ran a gel GEL ELECTROPHORESIS PROTOCOL : (24)

•Digested PVeg+XylR 1,5,7,10,13,16 with E,S; E0040+B0014 3,4,5,10,11,19,21,22 with X,P; B0079+GusA 3,4,5 E,S LIQUID CULTURE.

1-3B0079+GusA E,S 3.
4-9. PVeg+XylR E,S 1.
10-17. E0040+B0014 X,P 3.
18. 1 kb ladder.

1.A3 PCR.

E0040+B0014 X,P 4 to extract

08/31/12

•Ran a gel GEL ELECTROPHORESIS PROTOCOL : (25)

•Dephosphorylated:
Ω+AmyE 3’ S,P
Ω+AmyE 3’ II S,P
6 AraC+ Ω+AmyE 3’ E,X
8 AraC+ Ω+AmyE 3’ E,X
11 AraC+ Ω+AmyE 3’ E,X
12 AraC+ Ω+AmyE 3’ E,X

•Ran a gel with A3 PCR GEL ELECTROPHORESIS PROTOCOL : (26)

•It was the second time we didn’t obtain a band from A3’s PCR.

•Probably because it had been missing the buffer 2’s ethanol (“blue lid”) from the PCR purification.

•Ran a gel woth E0040+B0014 X,P 4 to extract
Gen extraction protocol.

•Did an A3 PCR.

SEPTEMBER

1.A3 PCR 1.
2.A3 PCR 2.
3.E0040+B0014 X,P 1.
4.E0040+B0014 X,P 2.
5.Ω+AmyE 3’ dephosphorylated S,P.
6.Ω+AmyE 3’ dephosphorylated S,P II.
7.97 dephosphorylated S,P.
8.98 dephosphorylated S,P.
9.99 dephosphorylated S,P.
10-13. Arac+ Ω+AmyE 3’ dephosphorylated E,X 12.
14. 1 kb Ladder.

09/01/12

•Ran a gel with GEL ELECTROPHORESIS PROTOCOL : (28)

•Ligated E0040+B0014 X,P 2 +promoter S,P dephosphorylated; K143002 X,P+ Ω+AmyE 3’ dephosphorylated S,P LIGATION PROTOCOL.

09/03/12

•Digested B0079+GusA E,S 3,4,5; PVeg+XylR E,S 1,5,7,10,13,16 LIQUID CULTURE.

09/04/12

•Ran gel with digestions:
B0079+GusA E,S 3,4,5
PVeg+XylR E,S 1,5,7,10,13,16
GEL ELECTROPHORESIS PROTOCOL .

•Purified A3 PCR 1,2.

•Ran a gel of A3 PCR
GEL ELECTROPHORESIS PROTOCOL and digested with X,P LIQUID CULTURE.

•From ligations: PVeg+E0040+B0014, PBad/PXyl+E0040+B0014, B0079+E0040+B0014 only colonies grew in PBad/PXyl+E0040+B0014.

•Plated colonies that grew in a new plate.

•Made liquid cultures of these
LIQUID CULTURE.

•Repeated the ones that did not grow.

•Digested E0040+B0014 4 with X,P LIQUID CULTURE.

•Ran a gel GEL ELECTROPHORESIS PROTOCOL .

•Extracted from gel LIQUID CULTURE.
-BBa_J23101 18E plate 1 plasmid BBa_J61002_2948 bp Amp+

24 PBad/PXyl+E0040+B0014 tubes we extracted

1.E0040+B0014 X,P
2.E0040+B0014 X,P
3.PVeg+XylR E
4.B0079+GusA S
5.1 kb plus ladder
Extracted band from 1. and 2

Digested B0079+GusA with E,S 4,5; PVeg+XylR with E,S

09/05/12

•From the 24 PBad/PXyl+E0040+B0014 tubes we extracted plasmids (29) and ran a gel LIQUID CULTURE.

•Extracted plasmid from 2 tubes of E0040+B0014.

•Ran a gel with yesterday’s digestions:
1.E0040+B0014 X,P
2.E0040+B0014 X,P
3.PVeg+XylR E
4.B0079+GusA S
5.1 kb plus ladder

•Extracted band from 1. and 2. LIQUID CULTURE.

•Purified A3 PCR from 2 0.6ml tubes 1 and 2.

•1 colony grew from ligation pVeg+E0040+B0014.

•We streaked this in another plate and did liquid cultures
LIQUID CULTURE.

•To do:
•Ligate B0079 S,P dephosphorylated + E0040+B0014 X,P and Ω+AmyE 3’ S,P dephosphorylated+ K143001 X,P.
•Digested B0079+GusA with E,S 4,5; PVeg+XylR with E,S 10,13. (31)

•A3 PCR and gel A3 PCR X,P

09/06/12

•A3 PCR and gel A3 PCR X,P 1,2.

09/14/12

•Digested Ω+AmyE 3’ 11,13,18, and 22 with E,X.
•Ligate:
PVeg S,P dephosphorylated+XylR X,P.
PBad p Xyl S,P dephosphorylated + E0040+B0014 X,P.
pSB13C3 E,P dephosphorylated + A3 PCR E,P.
pSB13C3 E,P dephosphorylated + GusA PCR E,P.
pSB13C3 E,P dephosphorylated + XylR E,P.
pSB13C3 E,P dephosphorylated + pVeg E,P.
pSB13C3 E,P dephosphorylated + pBad pXyl E,P.
pSB13C3 E,P dephosphorylated + Ω PCR E,P.

09/16/12

• Colonies in these plates grew:
- R0079+E0040+B0014
- pBad/pXyl
- XylR
- pVeg
- A3+E0040+B0014 from colonies 1,3,4,5,6,7,8,9,10,11,12,13,14,15,17
- pVeg+E0040+B0014 1,2,3,4,5,6,8,9,10,11,12,13,14,15,16
- pBad/pXyl+E0040+B0014 2 tubes from the same correct colony.
- pVeg+XylR 1,2
- pBad/pXyl+pSB1C3 1,2
- XylR+pSB1C3 1,2
- pVeg+pSB1C3 1,2
- A3+pSB1C3 1,2
- GusA+pSB1C3 1,2
- omegacassette+pSB1C3 1,2

• Ran gel from the plasmid extractions that we did yesterday:
- A3+E0040+B0014 1-16
- pVeg+E0040+B0014 1-16, 18
- omega cassette+AmyE 3’ 11,13,18,22
• Digested R0079+E0040+B0014 with E,S. to ligate with AmyE 3’ E,x dephosphorylated.
• Digested omega cassette with E,P.
• Digested pSB1C3 with E,P.
• Made liquid cultures from AmyE 5’ and AmyE 3’.
• Did plasmid extraction from pSB1C3 colonies 3 and 6.

09/17/12

• Digested A3+E0040+B0014 colonies 2,3,4,5,6,11 and 16 with E,S.
• Digested pVeg+E0040+B0014 colonies 1,2,3,4,5,9 and 10 with E,S.
• Dephosphorylated omega cassette+AmyE 3’ colonies 13,18 and 22 digested with E,X.
• Digested pBad/pXyl and pVeg with S,P. Then dephosphorylated.
• Digested AmyE 3’ with E,X. Then dephosphorylated.

09/18/12

• Ran gel with:
1. A3 2 E,S
2. A3 3 E,S
3. A3 4 E,S
4. A3 5 E,S
5. A3 6 E,S
6. A3 11 E,S
7. A3 16 E,S
8. E0040+B0014 colony 1 E,X
9. AmyE 5’ E,P
10. AmyE 3’ E,X
11. Omega cassette E,S
12. pSB1C3 E,P
13. ladder
Bottom:
1. pVeg 1 E,S
2. pVeg 2 E,S
3. pVeg 3 E,S
4. pVeg 4 E,S
5. pVeg 5 E,S
6. pVeg 9 E,S
7. pVeg 10 E,S
8. pVeg S,P dephosphorylated
9. pVeg 2 S,P
10. pBad/pXyl S,P
11. XylR X,P
12. R0079+GFP+TT E,S
13. R0079 S,P
14. Ladder
• Dephosphorylated GFP+TT E,X; AmyE 5’ E,X; pSB1C3 E,P; pVeg 2 S,P; pBad/pXyl S,P and R0079 S,P.

09/19/12

• Did PCR from A3 and a 1/50 dilution.
• Ran gel with:
1. pVeg 3 E,P.
2. pVeg 9 E,P.
3. pVeg 10 E,P.
4. pBAd/pXyl 3 E,P.
5. pBAd/pXyl 5 E,P.
6. pBAd/pXyl 1 E,P.
7. A3 3 E,P.
8. A3 4 E,P.
9. XylR 1 E,P.
10. XylR 3 E,P.
11. XylR 8 E,P.
12. pSB1C3 6 E,P.
13. pSB1C3 6 E,P.
14. AmyE 5’ E,S.
15. AmyE 5’ E,S.
16. A3 1/50 PCR.
17. A3 PCR.
18. Ladder
• We did transformations:
- 2 of R0079+GusA
- R0079+GusA control
- 2 of A3+pSB1AK3
- A3+pSB1AK3 control
- 2 of omega cassette+pSB1C3
- 2 of GusA+pSB1C3
• Digested:
- pVeg+pSB1C3
- pBad/pXyl+pSB1C3
- XylR+pSB1C3
- A3+pSB1C3
With E,P.
• Ran gel with these digestions.

09/19/12

• Made liquids cultures from:
- Glicerol of AmyE 5’
- Glicerol of AmyE 3’
- pBad/pXyl+pSB1C3 colony 5
• Made liquid cultures from yesterday transformations:
- R0079+GusA 2 and control
- A3+pSB1AK3 2 and control
- Omega cassette+pSB1C3 2
- GusA+pSB1C3 2
• We transformed yesterday ligations:
- pBad/pXyl+pSB1C3
- XylR+pSB1C3
- pVeg+pSB1C3
- A3+pSB1C3
• Purified A3 PCR with kit, and then, digested with E,P and E,S.
• Ran gel

09/20/12

• Made liquid cultures from transformations:
- Omega cassette+pSB1C3 colony 7
- 2 of GusA+pSB1C3 colony 32
- R0079+GusA colony 12
• Digested A3 1/50 PCR with E,P and E,S.
• Made liquid cultures from R0079+E0040+B0014; pBad/pXyl+E0040+B0014; pVeg+E0040+B0014; A3+E0040+B0014.
• Ligated:
- pBad/pXyl S,P dephosphorylated + E0040+B0014 X,P
- pVeg S,P dephosphorylated + E0040+B0014 X,P
- A3 PCR E,S + E0040+B0014 E,X dephosphorylated.

09/21/12

• Ran gel with:
1. R0079+GFP+TT 1
2. R0079+GFP+TT
3. pBad/pXyl+pSB1C3 1
4. pBad/pXyl+pSB1C3
5. omega cassette+psB1C3 1
6. omega cassette+psB1C3
7. pSB1C3 E,P 1
8. pSB1C3 E,P
9. pSB1C3 E
10. pSB1C3 P
11. A3 1/50 PCR E,P

09/22/12

• Ran gel with lysis extractions:
1. GusA+pSB1C3 1
2. GusA+pSB1C3 2
3. GusA+pSB1C3 3
4. GusA+pSB1C3 4
5. GusA+pSB1C3 5
6. GusA+pSB1C3 6
7. GusA+pSB1C3 7
8. GusA+pSB1C3 8
9. GusA+pSB1C3 9
10. GusA+pSB1C3 10
11. GusA+pSB1C3 11
12. GusA+pSB1C3 12
13. pSB1C3
14. A3+E0040+B0014 1
15. A3+E0040+B0014 2
16. A3+E0040+B0014 3
17. A3+E0040+B0014 4
18. A3+E0040+B0014 5
19. A3+E0040+B0014 6
20. A3+E0040+B0014 7
21. A3+E0040+B0014 8
22. A3+E0040+B0014 9
23. pVeg+E0040+B0014 3
24. pVeg+E0040+B0014 4
25. pVeg+E0040+B0014 5
26. pVeg+E0040+B0014 6
27. pVeg+E0040+B0014 7
28. pVeg+E0040+B0014 8
29. pVeg+E0040+B0014 9
30. pVeg
31. pBad/pXyl+E0040+B0014 1
32. pBad/pXyl+E0040+B0014 2
33. pBad/pXyl+E0040+B0014 3
34. pBad/pXyl+E0040+B0014 4
35. pBad/pXyl+E0040+B0014 5
36. pBad/pXyl+E0040+B0014 6
37. pBad/pXyl+E0040+B0014 7
38. pBad/pXyl+E0040+B0014 8
39. pBad/pXyl+E0040+B0014 9
40. pBad/pXyl+E0040+B0014 10
41. pBad/pXyl
42. pVeg+XylR 1
43. pVeg+XylR 2
44. pVeg+XylR 3
45. pVeg+XylR 4
46. pVeg+XylR 5
47. pVeg+XylR 6
48. pVeg+XylR 7
49. pVeg+XylR 8
50. omega cassette

• Ran gel with yesterday digestions:
1. R0079+GFP+TT E,P
2. R0079+GFP+TT E,P
3. Omega cassette+pSB1C3 E,P
4. Omega cassette+pSB1C3 E,P
5. Ladder
6. pBad/pXyl+pSB1C3
7. pBad/pXyl+pSB1C3
8. pSB1C3 6 E,P.
9. A3 1/50 PCR E,S
10. pBbak C011
11. pBbak C012
12. ladder

• Did pellet from R0079+GusA.
• Did plasmid extraction from omega cassette+pSB1C3 colonies 1,4,6 and 7.
• Digested them with E,P.
• Digested:
- GusA+pSB1C3 1,3,4,10 and 11
- A3+E0040+B0014 2,4,7 and 9
- pVeg+E0040+B0014 4,5 and 6
- pBad/pXyl+E0040+B0014 3,7 and 10
- pVeg+XylR 2,4 and 5
with E,P.
• Made liquid cultures from pVeg+pSB1C3
• Ligated:
- XylR E,P + pSB1C3 E,P dephosphorylated.
- pVeg E,P + pSB1C3 E,P dephosphorylated.
- A3 1/50 PCR E,P + pSB1C3 E,P dephosphorylated.
- pBad/pXyl S,P dephosphorylated + E0040+B0014 X,P.
- pVeg S,P dephosphorylated + E0040+B0014 X,P.
- A3 1/50 PCR E,S + E0040+B0014 E,X dephosphorylated.
- pVeg S,P dephosphorylated + XylR X,P.

09/23/12

• Ran gel with yesterday digestions:
1. Omega cassette+pSB1C3 1 E,P
2. Omega cassette+pSB1C3 4 E,P
3. Omega cassette+pSB1C3 6 E,P
4. Omega cassette+pSB1C3 7 E,P
5. GusA+pSB1C3 1 E,P
6. GusA+pSB1C3 3 E,P
7. GusA+pSB1C3 4 E,P
8. GusA+pSB1C3 10 E,P
9. GusA+pSB1C3 11 E,P
10. pSB1C3 E,P dephosphorylated
11. pVeg+XylR 2 E,P
12. pVeg+XylR 4 E,P
13. pVeg+XylR 5 E,P
14. pVeg S,P dephosphorylated
15. pVeg+GFP+TT 4 E,P.
16. pVeg+GFP+TT 5 E,P.
17. pVeg+GFP+TT 6 E,P.
18. ladder
Bottom
1. pBad/pXyl+GFP+TT 3 E,P
2. pBad/pXyl+GFP+TT 7 E,P
3. pBad/pXyl+GFP+TT 10 E,P
4. pBad/pXyl S,P dephosphorylated
5. A3+GFP+TT 2 E,P
6. A3+GFP+TT 4 E,P
7. A3+GFP+TT 7 E,P
8. A3+GFP+TT 9 E,P
9. Ladder

09/24/12

• Did PCR from omega cassette+pSB1C3 colonies 1,4,6 and 7.
• Made 1/50 dilutions from these PCR products.
• Ran gel with:
1. Omega cassette+pSB1C3 1/50 PCR 1
2. Omega cassette+pSB1C3 PCR 1
3. Omega cassette+pSB1C3 1/50 PCR 4
4. Omega cassette+pSB1C3 PCR 4
5. Omega cassette+pSB1C3 1/50 PCR 6
6. Omega cassette+pSB1C3 PCR 6
7. Omega cassette+pSB1C3 1/50 PCR 7
8. Omega cassette+pSB1C3 PCR 7
9. GusA+pSB1C3 1 P
10. GusA+pSB1C3 3 P
11. GusA+pSB1C3 4 P
12. GusA+pSB1C3 10 P
13. GusA+pSB1C3 11 P
14. pVeg+pSB1C3 6 E,P
15. pVeg+pSB1C3 5 E,P
16. pVeg+pSB1C3 4 E,P
17. pVeg+pSB1C3 3 E,P
18. pVeg+pSB1C3 2 E,P
19. pVeg+pSB1C3 1 E,P
20. ladder

• From yesterday transformations, these didn’t grow:
- pBad/pXyl+E0040+B0014 1 and 2.
- A3+E0040+B0014.
• Made liquid cultures from transformations that did grow:
- pVeg+E0040+B0014.
- pVeg+XylR.
- A3+pSB1C3
- pVeg+pSB1C3
- XylR+pSB1C3

09/26/12

• Did plasmid extractions form liquids cultures:
- 8 of pVeg+pSB1C3
- 8 of A3
- 8 of XylR
• Digested them with E,P.
• Ran gel with:
1. Ladder
2. XylR+pSB1C3 1 E,P
3. XylR+pSB1C3 2 E,P
4. XylR+pSB1C3 3 E,P
5. pVeg+pSB1C3 1 E,P
6. pVeg+pSB1C3 3 E,P
7. pVeg+pSB1C3 4 E,P
8. pVeg+pSB1C3 5 E,P
9. pVeg+pSB1C3 6 E,P
10. pVeg+pSB1C3 8 E,P
11. pSB1C3 6 E,P dephosphorylated
12. A3+pSB1C3 1 E,P
13. A3+pSB1C3 3 E,P
14. A3+pSB1C3 4 E,P
15. A3+pSB1C3 5 E,P
16. A3+pSB1C3 6 E,P
17. A3+pSB1C3 8 E,P
18. Ladder
19. P4+E0040+B0014 1 E,X
20. P4+E0040+B0014 7 E,X

09/27/12

• Digested pVeg+XylR colonies 1,4,5 and 6 in pJ209 plasmid with E,S for 3 hours.
• Digested pVeg+E0040+B0014 colonies 7,9,10 and 11 in pasmid pJ209 with E,P.

10/09/12

• Ligated:
- A3 1/50 PCR E,P + pSB1C3 6 E,P dephosphorylated.
- pVeg S,P dephosphorylated + XylR X,P.
- P4+CI+E1010+B0014 E,X dephosphorylated + AmyE 5’+pBad/pXyl E,S.

10/10/12

• Ligated:
- GusA PCR E,P + pSB1C3 6 E,P dephosphorylated.
- pBad/pXyl S,P dephosphorylated + E0040+B0014 X,P.
- pVeg S,P dephosphorylated + E0040+B0014 X,P.
- A3 1/50 PCR E,S + E0040+B0014 E,X dephosphorylated.
• Digested R0079+E0040+B0014 with E,S.
• Digested AmyE 3’ with E,X. Then dephosphorylated.
• Digested pVeg and R0079, A3 with X,P.
• Digested pBad/pSB1C3 with S,P.

10/11/12

• Did plasmid extraction from liquid cultures:
- 2 of AmyE 5’
- 2 of AmyE 3’
- 2 of E0040+B0014
• Ran gel with:
1. A3 1/50 PCR X,P
2. A3 1/50 PCR X,P
3. A3+pSB1C3 6 X,P
4. A3+pSB1C3 6 X,P
5. A3+pSB1C3 8 X,P
6. A3+pSB1C3 8 X,P
7. pVeg X,P
8. pVeg 96 X,P
9. pVeg 96 X,P
10. pVeg+pSB1C3 1 X,P
11. pVeg+pSB1C3 1 X,P
12. pVeg+pSB1C3 3 X,P
13. pVeg+pSB1C3 3 X,P
14. R0079 X,P
15. Ladder

10/12/12

• Ligated: - AmyE 5’+pBad/pXyl 10 E,S + P4+CI+E1010+TT E,X dephosphorylated.
- AmyE 5’+pBad/pXyl 11 E,S + P4+CI+E1010+TT E,X dephosphorylated.
- AmyE 5’+pBad/pXyl 12 E,S + P4+CI+E1010+TT E,X dephosphorylated.
- pVeg S,P dephosphorylated + XylR X,P.
- A3 1/50 PCR E,P + pSB1C3 E,P dephosphorylated.

10/12/12

• Digested AmyE 5’ with S,P
• Dephosphorylated it.
• Ligated:
- AmyE 5’ S,P dephosphorylated with
- R0079 X,P
- pVeg 96 X,P
- A3 1/50 PCR X,P
- A3+pSB1C3 6 X,P
- R0079+E0040+B0014
• Ligated pBad/pXyl+pSB1C3 S,P dephosphorylated + E0040+B0014 X,P.
• Ran gel with:
1. A3+pSB1C3 1
2. A3+pSB1C3 2
3. A3+pSB1C3 3
4. A3+pSB1C3 4
5. A3+pSB1C3 5
6. A3+pSB1C3 6
7. A3+pSB1C3 7
8. A3+pSB1C3 8
9. A3+pSB1C3 9
10. A3+pSB1C3 10
11. A3+pSB1C3 11
12. A3+pSB1C3 6 control
13. AmyE 5’+P4+CI+E1010+B0014 1
14. AmyE 5’+P4+CI+E1010+B0014 2
15. AmyE 5’+P4+CI+E1010+B0014 3
16. AmyE 5’+P4+CI+E1010+B0014 4
17. AmyE 5’+P4+CI+E1010+B0014 5
18. AmyE 5’+P4+CI+E1010+B0014 6
19. AmyE 5’+P4+CI+E1010+B0014 7
20. P4+CI+E1010+B0014 1 control

10/09/12

• Ligate:
K143001+pBad/pXyl + p4+CI+E1010+TT E,X dephosphorylated.
• Ligate:
pVeg S,P dephosphorylated + XylR X,P.
• Ligate:
A3 PCR 1/50 E,P + pSB1C3 E,P dephosphorylated

10/13/12

• Digested AmyE 5’ with S,P. Then dephosphorylated.
• Ligate:
AmyE 5’ S,P dephosphorylated +
- R0079 X,P
- pVeg 96 X,P
- A3 PCR 1/50 X,P
- A3+pSB1C3 colony 6 X,P
- R0079+E0040+B0014 E,X
• Ligate:
pBad/pXyl+pSB1C3 S,P dephosphorylated + E0040+B0014 X,P

• Ran a gel with:
1. A3+pSB1C3 1
2. A3+pSB1C3 2
3. A3+pSB1C3 3
4. A3+pSB1C3 4
5. A3+pSB1C3 5
6. A3+pSB1C3 6
7. A3+pSB1C3 7
8. A3+pSB1C3 8
9. A3+pSB1C3 9
10. A3+pSB1C3 10
11. A3+pSB1C3 11
12. A3+pSB1C3 6 control
13. AmyE 5’+P4+CI+E1010+B0014 8
14. AmyE 5’+P4+CI+E1010+B0014 9
15. AmyE 5’+P4+CI+E1010+B0014 10
16. P4+CI+E1010+B0014 1 control
17. pVeg+XylR 1
18. pVeg+XylR 2
19. pVeg+XylR 3
20. pVeg+XylR 4
21. pVeg+XylR 5
22. pVeg+XylR 6
23. pVeg+XylR 7
24. pVeg+XylR 8
25. pVeg+XylR 10
26. pVeg+XylR 11
27. pVeg+XylR 12
28. pVeg 96 control

• Ran gel with:
1. A3 1/50 PCR X,P
2. A3+pSB1C3 6 X,P
3. pVeg 96 X,P
4. pVeg+pSB1C3 1 X,P
5. pVeg+pSB1C3 3 X,P
6. R0079 X,P
7. pBad/pXyl+pSB1C3 S,P dephosphorylated
8. ladder
9. Digested:
- A3+pSB1C3 colonies 3,4,5 and 10 with E,P.
- AmyE 5’+pBad/pXyl+P4+CI+E1010*B0014 colonies 1,2,7 and 8 with E,P.
- pVeg+XylR 1,4,5 and 12 with E,P.
• Ran gel with:
1. GFP+TT 1 X,P
2. GFP+TT 1 X,P
3. GFP+TT 1 E,S
4. GFP+TT 1 E,S
5. GFP+TT 2 X,P
6. GFP+TT 2 X,P
7. GFP+TT 2 E,S
8. GFP+TT 2 E,S
9. Ladder
10. A3 1/50 PCR X,P
11. A3+pSB1C3 6 X,P
12. pVeg 96 X,P
13. pVeg+pSB1C3 1 X,P
14. R0079 X,P
15. AmyE 5’ S,P

10/16/12

• Made liquid cultures from yesterday transformations:
- AmyE 5’+R0079
- AmyE 5’+R0079_2
- AmyE 5’+A3
- AmyE 5’+pVeg
- pBad/pXyl+E0040+B0014 in pSB1C3 plasmid.
• Digested:
- AmyE 5’+pBad/pXyl+P4+CI+E1010+B0014 colonies 1,2,7 and 8 with E,P.
- pVeg+XylR 1,4,5 and 12 with E,P.
- R0079+GFP+TT and R0079+GFP+TT_2 with X,P.

@@ Line 1: / Line 1: @@
 {{:Template:Team:UNAM_Genomics_Mexico/webhtml| content=
+__NOTOC__
 <br />
-<center><h1>'''Arabinose/Xylose AND Gate'''</h1></center>
+<center><h1>'''Arabinose/Xylose AND Gate Notebook'''</h1></center>
 <br />
 <br />
-<table border="0"  height="150" cellspacing="15" bgcolor="transparent" id="tablecontentbg">
+<table border="0"  height="150" cellspacing="15" bgcolor="transparent" id="tablecontentbg" cellpadding="20">
 <tr>
-<td id="leftcolumn2">Nanotubes!!</td>
+<td id="leftcolumn2"><center>2 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#JUNE | '''JUNE''']] </center> <br />
-<td  id="contentcolumn2">The logic</td>
+<br />
-<td id="rightcolumn2">Random info</td>
+.1 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#06.2F07.2F12 |06/07/12]] <br />
+.2 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#06.2F12.2F12 |06/12/12]] <br />
+.3 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#06.2F13.2F12 |06/13/12]] <br />
+.4 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#06.2F14.2F12 |06/14/12]] <br />
+.5 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#06.2F15.2F12 |06/15/12]] <br />
+.6 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#06.2F18.2F12 |06/18/12]] <br />
+.7 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#06.2F19.2F12 |06/19/12]] <br />
+.8 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#06.2F22.2F12 |06/22/12]] <br />
+.9 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#06.2F25.2F12 |06/25/12]] <br />
+.10 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#06.2F26.2F12 |06/26/12]] <br />
+.11 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#06.2F27.2F12 |06/27/12]] <br />
+.12 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#06.2F29.2F12 |06/29/12]] <br />
+</td>
+<td id="contentcolumn2"><center>3 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#JULY | '''JULY''']] </center> <br />
+<br />
+.1[[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#07.2F03.2F12 | 07/03/12]] <br />
+.2 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#07.2F04.2F12 | 07/04/12]] <br />
+.3 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#07.2F06.2F12 | 07/06/12]] <br />
+.4 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#07.2F07.2F12 | 07/07/12]] <br />
+.5 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#07.2F08.2F12 | 07/08/12]] <br />
+.6 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#07.2F09.2F12 | 07/09/12]] <br />
+.7 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#07.2F10.2F12 | 07/10/12]] <br />
+.8 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#07.2F11.2F12 | 07/11/12]] <br />
+.9 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#07.2F12.2F12 | 07/12/12]] <br />
+.10 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#07.2F13.2F12 | 07/13/12]] <br />
+.11 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#07.2F14.2F12 | 07/14/12]] <br />
+.12 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#07.2F16.2F12 | 07/16/12]] <br />
+.13 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#07.2F17.2F12 | 07/17/12]] <br />
+.14 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#07.2F18.2F12 | 07/18/12]] <br />
+.15 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#07.2F19.2F12 | 07/19/12]] <br />
+.16 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#07.2F20.2F12 | 07/20/12]] <br />
+.17 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#07.2F23.2F12 | 07/23/12]] <br />
+.18 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#07.2F24.2F12 | 07/24/12]] <br />
+.19 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#07.2F25.2F12 | 07/25/12]] <br />
+.20 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#07.2F26.2F12 | 07/26/12]] <br />
+.21 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#07.2F27.2F12 | 07/27/12]] <br />
+.22 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#07.2F30.2F12 | 07/30/12]] <br />
+.23 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#07.2F31.2F12 | 07/31/12]] <br />
+</td>
+<td id="rightcolumn2"><center>4 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#AUGUST | '''AUGUST''']] </center> <br />
+<br />
+.1 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#08.2F01.2F12 | 08/01/12]] <br />
+.2 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#08.2F02.2F12 | 08/02/12]] <br />
+.3 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#08.2F03.2F12 | 08/03/12]] <br />
+.4 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#08.2F06.2F12 | 08/06/12]] <br />
+.5 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#08.2F08.2F12 | 08/08/12]] <br />
+.6 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#08.2F09.2F12 | 08/09/12]] <br />
+.7 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#08.2F10.2F12 | 08/10/12]] <br />
+.8 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#08.2F13.2F12 | 08/13/12]] <br />
+.9 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#08.2F16.2F12 | 08/16/12]] <br />
+.10 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#08.2F20.2F12 | 08/20/12]] <br />
+.11 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#08.2F21.2F12 | 08/21/12]] <br />
+.12 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#08.2F22.2F12 | 08/22/12]] <br />
+.13 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#08.2F23.2F12 | 08/23/12]] <br />
+.14 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#08.2F24.2F12 | 08/24/12]] <br />
+.15 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#08.2F25.2F12 | 08/25/12]] <br />
+.16 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#08.2F28.2F12 | 08/28/12]] <br />
+.17 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#08.2F29.2F12 | 08/29/12]] <br />
+.18 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#08.2F30.2F12 | 08/30/12]] <br />
+.19 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#08.2F31.2F12 | 08/31/12]] <br />
+</td>
+</tr>
+<tr>
+<td id="leftcolumn2"><center>5 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#SEPTEMBER | '''SEPTEMBER''']] </center> <br />
+<br />
+.1 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#09.2F01.2F12 | 09/01/12]] <br />
+.2 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#09.2F02.2F12 | 09/03/12]] <br />
+.3 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#09.2F04.2F12 | 09/04/12]] <br />
+.4 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#09.2F05.2F12 | 09/05/12]] <br />
+.5 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#09.2F06.2F12 | 09/06/12]] <br />
+.6 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#09.2F14.2F12 | 09/14/12]] <br />
+.7 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#09.2F16.2F12 | 09/16/12]]<br />
+.8 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#09.2F17.2F12 | 09/17/12]]<br />
+.9 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#09.2F18.2F12 | 09/18/12]]<br />
+.10 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#09.2F19.2F12 | 09/19/12]]<br />
+.11 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#09.2F19.2F12 | 09/19/12]]<br />
+.12 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#09.2F20.2F12 | 09/20/12]]<br />
+.13 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#09.2F21.2F12 | 09/21/12]]<br />
+.14 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#09.2F22.2F12 | 09/22/12]]<br />
+.15 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#09.2F23.2F12 | 09/23/12]]<br />
+.16 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#09.2F24.2F12 | 09/24/12]]<br />
+.17 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#09.2F26.2F12 | 09/26/12]]<br />
+.18 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#09.2F27.2F12 | 09/27/12]]<br />
+</td>
+<td  id="contentcolumn2">
+'''OCTOBER'''<br />
+.19 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#10.2F09.2F12 | 10/09/12]]<br />
+.20 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#10.2F10.2F12 | 10/10/12]]<br />
+.21 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#10.2F11.2F12 | 10/11/12]]<br />
+.22 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#10.2F12.2F12 | 10/12/12]]<br />
+.23 [[Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#10.2F13.2F12 | 10/13/12]]<br />
+</td>
+<td id="rightcolumn2"><center>[[File:UnmagenomicsBacteria sugar.png | 190px]]</center><p> '''On hover the images to see descriptions'''</p><td/>
 </tr>
 </table>
 =JUNE=
@@ Line 37: / Line 138: @@
 plate 2 17E<br />
 Stock 50 mg/mL<br />
-E.coli 1/1000<br />
+''E.coli'' 1/1000<br />
 [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Transformation | TRANSFORMATION PROTOCOL]]. <br />
 We made liquid cultures with colonies [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Liquid_culture | LIQUID CULTURE]]. <br />
@@ Line 68: / Line 169: @@
 <h2>06/13/12</h2><br />
 We ran gel and extracted from gel [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Gel_extraction_protocol | LIQUID CULTURE]].<br />
-We made liquid cultures [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Liquid_culture | LIQUID CULTURE]] and lysed [LYSIS PROTOCOL]. <br />
+We made liquid cultures [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Liquid_culture | LIQUID CULTURE]] and lysed. <br />
 <br />
 <br />
@@ Line 197: / Line 298: @@
 <br />
 <br />
-<html>
-<div class='thumbnailWrapper'>
-<ul>
-<li>
-<img src='https://static.igem.org/mediawiki/2012/7/73/UnamgenomicsandsugarBitacora_7.jpg' height="300"/>
-<div class='captionaqua'>
-<p class='captionInside'>1.B0014 E,X<br />
-.B0014 E,P<br />
-. ΩSpr/Strr  E<br />
-.C0080 X,S<br />
-.E1010 X,S<br />
-.2 μl   ladder<br />
-</li>
-</ul>
-</div>
-<br /><br />
-</html>
 <h2>06/22/12</h2><br />
 >Ran gels with digestions B0014 with E,X and E,P [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Gel_electrophoresis | GEL ELECTROPHORESIS PROTOCOL]]. <br />
->Dephosphated B0014 E,X and B0014 E,P [DESPHOPHORYLATION PROTOCOL]. <br />
+>Dephosphated B0014 E,X and B0014 E,P. <br />
 <br />
@@ Line 267: / Line 352: @@
 <br />
 <br />
+::::::::::::::::::::::::::::::::::::::[[File:UnamgenomcisUp.png|right | 120px |link=Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#Arabinose.2FXylose_AND_Gate_Notebook]]
 =JULY=
@@ Line 313: / Line 400: @@
 >Did band extractions [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Gel_extraction_protocol | LIQUID CULTURE]]. <br />
 >Stored at -20ºC. <br />
->Did PCR to Cassete  ΩSpr/Strr   to add RBS and prefix/suffix [PCR PROTOCOL]. <br />
+>Did PCR to Cassete  ΩSpr/Strr   to add RBS and prefix/suffix. <br />
 >Left digesting with E,S [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Digestion_protocol_.2820_.C2.B5l.29 | LIQUID CULTURE]]. <br />
 <br />
@@ Line 338: / Line 425: @@
 <h2>07/04/12</h2><br />
->We dephosphated B0079 S,P, K143001 S,P, K143002 E,X (9.1) [DESPHOPHORYLATION PROTOCOL]. <br />
+>We dephosphated B0079 S,P, K143001 S,P, K143002 E,X (9.1). <br />
->Ligated Cassete  ΩSpr/Strr  +K143002 dephosphated(digested with E,X and E,S) LIGATION PROTOCOL]. <br />
+>Ligated Cassete  ΩSpr/Strr  +K143002 dephosphated(digested with E,X and E,S). <br />
 >Transformed ligation and left overnight plated [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Transformation | TRANSFORMATION PROTOCOL]]. <br />
->Extracted plasmid PBBR1 GusA in 2 1.5 mL eppendorfs [PLASMID  EXTRACTION (“soft” lysis) PROTOCOL]. <br />
+>Extracted plasmid PBBR1 GusA in 2 1.5 mL eppendorfs. <br />
 >Digested with PstI [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Digestion_protocol_.2820_.C2.B5l.29 | LIQUID CULTURE]]. <br />
 <br />
@@ Line 379: / Line 466: @@
 <li>
 <img src='https://static.igem.org/mediawiki/2012/1/13/UnamgenomicsandsugarBitacora_11.jpg' height="300"/>
-<div class='captionazul'>
+<div class='captiongray'>
 <p class='captionInside'>We dephosphated B0079 S,P, K143001 S,P, K143002 E,X<br />
+</p>
+</li>
+</ul>
+</div>
+<br /><br />
+</html>
+<html>
+<div class='thumbnailWrapper'>
+<ul>
+<li>
+<img src='https://static.igem.org/mediawiki/2012/b/b2/UnamgenomicsandsugarBitacora_11.1.jpg' height="300"/>
+<div class='captionnaranja'>
+<p class='captionInside'>1 PCR omega P<br />
+PCR omega I<br />
+PCR AraC P<br />
+PCR AraC I<br />
+ladder 1 Kb<br />
 </p>
 </li>
@@ Line 388: / Line 492: @@
 </html>
 <h2>07/09/12</h2><br />
-	From yesterday’s transformations only one colony grew. <br />
+From yesterday’s transformations only one colony grew. <br />
-	From the previous transformation only 2 colonies grew. <br />
+From the previous transformation only 2 colonies grew. <br />
-	These 3 were streaked in 3 plates: <br />
+These 3 were streaked in 3 plates: <br />
 DH5α  ΩSpr/Strr  +K143002  LB Km 30 Sp 100 1. <br />
 DH5α  ΩSpr/Strr  +K143002  LB Km 30 Sp 100 2. <br />
 DH5α  ΩSpr/Strr  +K143002  LB Km 30 Sp 100 3. <br />
 LB Km 30 Sp 100 control. <br />
-	Did liquid cultures in 3 tubes: <br />
+Did liquid cultures in 3 tubes: <br />
- ΩSpr/Strr  +K143002  LB Km 30 Sp 100 1. <br />
+ΩSpr/Strr  +K143002  LB Km 30 Sp 100 1. <br />
- ΩSpr/Strr  +K143002  LB Km 30 Sp 100 2. <br />
+ΩSpr/Strr  +K143002  LB Km 30 Sp 100 2. <br />
- ΩSpr/Strr  +K143002  LB Km 30 Sp 100 3. <br />
+ΩSpr/Strr  +K143002  LB Km 30 Sp 100 3. <br />
 LB Km30 Sp 100 control. <br />
 [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Liquid_culture | LIQUID CULTURE]]. <br />
-	Ran a gel with: (11) <br />
+Ran a gel with: (11) <br />
-	GusA P<br />
+GusA P<br />
-	PBBR1 GusA<br />
+PBBR1 GusA<br />
-	 Ω E PCR P<br />
+Ω E PCR P<br />
-	 Ω PCR P<br />
+Ω PCR P<br />
-	 Ω PCR I<br />
+Ω PCR I<br />
-	 Ω E<br />
+Ω E<br />
- Ω PCR I<br />
+Ω PCR I<br />
 [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Gel_electrophoresis | GEL ELECTROPHORESIS PROTOCOL]] <br />
-	Did GusA primers dissolution for PCR. <br />
+Did GusA primers dissolution for PCR. <br />
-	GusA PCR <br />
+GusA PCR <br />
-[PCR PROTOCOL] <br />
+Gel Extraction by kit of lanes 3 and 5 [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Gel_extraction_protocol | LIQUID CULTURE]]. <br />
-	Gel Extraction by kit of lanes 3 and 5 [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Gel_extraction_protocol | LIQUID CULTURE]]. <br />
-PCR omega P, PCR omega I, PCR AraC P, PCR AraC I<br />
+'''PCR omega P, PCR omega I, PCR AraC P, PCR AraC I'''<br />
-•	Add 10 μl  of each primer (LW and UP). <br />
+Add 10 μl  of each primer (LW and UP). <br />
-•	Add 3 μl  of plasmid (P). <br />
+Add 3 μl  of plasmid (P). <br />
-•	Add 30.4 μl   buffer. <br />
+Add 30.4 μl   buffer. <br />
-•	Add 5 μl   Mg. <br />
+Add 5 μl   Mg. <br />
-•	Add 8 μl   DNTp’s. <br />
+Add 8 μl   DNTp’s. <br />
-•	Add 42.6μl   H2O miliQ. <br />
+Add 42.6μl   H2O miliQ. <br />
-•	Add 1 μl   RTTG polymerase. <br />
+Add 1 μl   RTTG polymerase. <br />
-•	Centrifuge (spin) 8 secs. <br />
+Centrifuge (spin) 8 secs. <br />
-•	Add vegetable oil till the eppendorf is full. <br />
+Add vegetable oil till the eppendorf is full. <br />
-•	Place eppendorf 1 mL in thermocycler. <br />
+Place eppendorf 1 mL in thermocycler. <br />
-•	Run PCR with program “BERNA”. <br /><br />
+Run PCR with program “BERNA”. <br /><br />
-Ran gel with: <br />
+<html>
-PCR omega P<br />
+<div class='thumbnailWrapper'>
-PCR omega I<br />
+<ul>
-PCR AraC P<br />
+<li>
-PCR AraC I<br />
+<img src='https://static.igem.org/mediawiki/2012/4/4b/UnamgenomicsandsugarBitacora_11.2.jpg' height="300"/>
-ladder 1 Kb<br />
+<div class='captionverde'>
-(11.1)
+<p class='captionInside'>GusA digestions with X,P;  Ω+AmyE 3’ with E,X; AraC PCR with E,S <br />
+</p>
+</li>
+</ul>
+</div>
+<br /><br />
+</html>
+<h2>07/10/12</h2><br />
+•GusA digestions with X,P;  Ω+AmyE 3’ with E,X; AraC PCR with E,S (2 times)[[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Digestion_protocol_.2820_.C2.B5l.29 | DIGESTIONS]]. (11.2) <br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<h2>07/11/12</h2><br />
+•GusA PCR digestions with E,S;  Ω+AmyE 3’ with E,X [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Digestion_protocol_.2820_.C2.B5l.29 | LIQUID CULTURE]]. <br />
+•T.V. AraC PCR+ Ω+AmyE 3’  E,X dephosphated ligation [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Ligation | LIGATION PROTOCOL]]. <br />
+<html>
+<div class='thumbnailWrapper'>
+<ul>
+<li>
+<img src='https://static.igem.org/mediawiki/2012/0/0a/UnamgenomicsandsugarBitacora_12.jpg' height="300"/>
+<div class='captionrojo'>
+<p class='captionInside'>1. ladder. <br />
+. GusA PCR E,S. <br />
+. Ω+AmyE 3’ with E,X. <br />
+</p>
+</li>
+</ul>
+</div>
+<br /><br />
+</html>
+<h2>07/12/12</h2><br />
+•Ran a gel with yesterday’s digestions: (12) <br />
+[[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Gel_electrophoresis | GEL ELECTROPHORESIS PROTOCOL]] . <br />
+•Transformed AraC PCR+ Ω+AmyE 3’ ligation in two tubes [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Transformation | TRANSFORMATION PROTOCOL]]. <br />
+•From pfrc54 liquid cultures (A3) that were grown overnight we extracted plasmid. <br />
+•Made glycerols from 2 LB Km 30 Sp100 DH5α  Ω+AmyE 3’ plates and from 1 LB Amp100 pfrc54 (A3) plates with control[[Team:UNAM_Genomics_Mexico/Notebook/Protocols#GLYCEROL_PROTOCOL | GLYCEROL PROTOCOL]] . <br />
+•Ligated GusA PCR with B0014 E,X desphophorylated [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Ligation | LIGATION PROTOCOL]]. <br />
+•Digested Pfrc54 (A3) with S,P [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Digestion_protocol_.2820_.C2.B5l.29 | LIQUID CULTURE]]. <br />
+•Desphophorylated  Ω+AmyE 3’ E,X. <br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<html>
+<div class='thumbnailWrapper'>
+<ul>
+<li>
+<img src='https://static.igem.org/mediawiki/2012/0/0f/UnamgenomicsandsugarBitacora_13.jpg' height="300"/>
+<div class='captionrojo'>
+<p class='captionInside'>•Ran gel with pfrc54 S,P<br />
+</p>
+</li>
+</ul>
+</div>
+<br /><br />
+</html>
+<h2>07/13/12</h2><br /><br />
+•Ran gel with pfrc54 S,P [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Gel_electrophoresis | GEL ELECTROPHORESIS PROTOCOL]] . (13) <br />
+•Transformation of GusA PCR + B0014 ligation [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Transformation | TRANSFORMATION PROTOCOL]]. <br />
+•Transformed with GFP E0040 psBIA2. <br />
+•Liquid Cultures with ligation: AraC+ Ω+AmyE 3’ for plasmid extraction at night [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Transformation | TRANSFORMATION PROTOCOL]]. <br />
+•''B. Subtitils'' competent cells. <br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<h2>07/14/12</h2><br /><br />
+•From 24 AraC+ Ω+AmyE 3’ LB Km 30 Sp 100 DH5α tubes: <br />
+•Extracted pellets<br />
+•Extracted plasmids. <br />
+•Ran gel [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Gel_electrophoresis | GEL ELECTROPHORESIS PROTOCOL]] . <br /><br />
+•From transformed DH5α km 30: <br />
+GusA+B0014 DH5α Km50 24 pellets <br />
+E0040 DH5α LB Amp100 <br />
+From these two we: <br />
+•Did liquid cultures [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Liquid_culture | LIQUID CULTURE]]. <br />
+•Extracted plasmid. <br />
+•From the GusA+E0014 transformation we took 24 colonies, did liquid cultures and extracted plasmid  [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Liquid_culture | LIQUID CULTURE]]. <br />
+•Ran gel with this transformation [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Gel_electrophoresis | GEL ELECTROPHORESIS PROTOCOL]] . <br />
+<br />
+<br />
+<br />
+<h2>07/16/12</h2><br /><br />
+•Digested E,P AraC+ Ω+AmyE 3’ <br />
+•Ω+AmyE 3’ E,P [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Digestion_protocol_.2820_.C2.B5l.29 | LIQUID CULTURE]]. <br />
+<br />
+<br />
+<html>
+<div class='thumbnailWrapper'>
+<ul>
+<li>
+<img src='https://static.igem.org/mediawiki/2012/4/48/UnamgenomicsandsugarBitacora_14.jpg' height="300"/>
+<div class='captionrosa'>
+<p class='captionInside'>Digested E,P AraC+ Ω+AmyE 3’ <br />
+Ω+AmyE 3’ E,P <br />
+</p>
+</li>
+</ul>
+</div>
+<br /><br />
+</html>
+<h2>07/17/12</h2><br /><br />
+•Ran gel with yesterday’s digestions [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Digestion_protocol_.2820_.C2.B5l.29 | LIQUID CULTURE]]. (14) <br />
+•The gel we ran didn’t work, probably because the agarose was not prepared correctly. <br />
+•Digested 12, 15, 18, 21 with AraC+ Ω+AmyE 3 with E and also with P’; B0014 with E,X; E0040 with X,S[[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Digestion_protocol_.2820_.C2.B5l.29 | LIQUID CULTURE]]. <br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<html>
+<div class='thumbnailWrapper'>
+<ul>
+<li>
+<img src='https://static.igem.org/mediawiki/2012/d/db/Bitacora_15.jpg' height="300"/>
+<div class='captionaqua'>
+<p class='captionInside'>•Digested 12, 15, 18, 21 with AraC+ Ω+AmyE 3 with E and also with P’; B0014 with E,X; E0040 with X,S<br />
+</p>
+</li>
+</ul>
+</div>
+<br /><br />
+</html>
+<br />
+<h2>07/18/12</h2><br /><br />
+•From yesterday’s digestions we ran a gel [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Gel_electrophoresis | GEL ELECTROPHORESIS PROTOCOL]] . (15) <br /><br />
+•We made liquid cultures of AraC+ Ω+AmyE 3’ 12, 15, 21 [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Liquid_culture | LIQUID CULTURE]]. <br /><br />
+•We ligated AraC PCR E,S dephosphated with + Ω+AmyE 3’ [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Ligation | LIGATION PROTOCOL]]. <br /><br />
+•We digested 1 + Ω+AmyE 3’ E,P [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Digestion_protocol_.2820_.C2.B5l.29 | LIQUID CULTURE]]. <br /><br />
+<h2>07/19/12</h2><br /><br />
+•We ran We digested 1 + Ω+AmyE 3’ E,P with Miguel’s enzymes and with Abiel’s enzymes [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Digestion_protocol_.2820_.C2.B5l.29 | LIQUID CULTURE]]. <br /><br />
+•We transformed with ligations AraC+ Ω+AmyE 3’ E and + Ω+AmyE 3’ E [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Transformation | TRANSFORMATION PROTOCOL]]. <br /><br />
+•Extracted plasmids from AraC+ Ω+AmyE 3’ 12,15,21. <br /><br />
+•Digested E0040 X,S 2,3,4,5,6; ligations AraC+ Ω+AmyE 3’ E 12,15,21; ligations AraC+ Ω+AmyE 3’ P [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Digestion_protocol_.2820_.C2.B5l.29 | LIQUID CULTURE]]. <br /><br />
+<br />
+<br />
+<html>
+<div class='thumbnailWrapper'>
+<ul>
+<li>
+<img src='https://static.igem.org/mediawiki/2012/f/f3/UnamgenomicsandsugarBitacora_16.jpg' height="300"/>
+<div class='captionmoradoclaro'>
+<p class='captionInside'>Digested E0040 X,S 2,3,4,5,6; ligations AraC+ Ω+AmyE 3’ E 12,15,21; ligations AraC+ Ω+AmyE 3’ P <br />
+</p>
+</li>
+</ul>
+</div>
+<br /><br />
+</html>
+<h2>07/20/12</h2><br /><br />
+•Ran gel with yesterday’s digestions [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Gel_electrophoresis | GEL ELECTROPHORESIS PROTOCOL]] . (16) <br />
+•Transformed GusA+B0014 in two tubes [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Transformation | TRANSFORMATION PROTOCOL]]. <br />
+•Made liquid cultures from AraC+ Ω+AmyE 3’s transformation LB Km30 Sp 100 and control LB Km 30 Sp100 [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Liquid_culture | LIQUID CULTURE]]. <br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<h2>07/23/12</h2><br /><br />
+•From 24 GusA+B0014 tubes (-) we didn’t do anything. <br />
+•From 4 AraC+ Ω+AmyE 3’  we extracted plasmid. <br />
+•Digested from the 4 AraC+ Ω+AmyE 3’   E,X; X; P and GusA PCR with X,P [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Digestion_protocol_.2820_.C2.B5l.29 | LIQUID CULTURE]]. <br /><br />
+<h2>07/24/12</h2><br /><br />
+•Digested B0014 E with X
+B0014 X with E<br />
+•Digested AraC+ Ω+AmyE 3’   1,2,3,4 with E,P [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Digestion_protocol_.2820_.C2.B5l.29 | LIQUID CULTURE]]. <br />
+<h2>07/25/12</h2><br /><br />
+•Ran gel of digested AraC+ Ω+AmyE 3’   1,2,3,4 with E,P  [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Digestion_protocol_.2820_.C2.B5l.29 | LIQUID CULTURE]]. <br />
+•Joined B0014 E with X B0014 X with E digestions. <br />
+•Made liquid cultures from 2 days old plated GusA+B0014 and extracted plasmid [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Liquid_culture | LIQUID CULTURE]]. Transformed [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Transformation | TRANSFORMATION PROTOCOL]]. <br />
+•From LasR DH5α make liquid cultures and plate [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Liquid_culture | LIQUID CULTURE]]. <br />
+•Digested  Ω+AmyE 3’  with X,P; E,S; C0080 X,P; E,S; S,P [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Digestion_protocol_.2820_.C2.B5l.29 | LIQUID CULTURE]]. <br />
+•Ligated Gus PCR X,P with B0079 S,P dephosphorylated [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Ligation | LIGATION PROTOCOL]]. <br /><br />
+<html>
+<div class='thumbnailWrapper'>
+<ul>
+<li>
+<img src='https://static.igem.org/mediawiki/2012/8/84/UnamgenomicsandsugarBitacora_17.jpg' height="300"/>
+<div class='captionazul'>
+<p class='captionInside'>1.Ω+AmyE 3’ X,P<br />
+. Ω+AmyE 3’ E,S<br />
+.C0080 X,P<br />
+.C0080 E,S<br />
+.C0080 S,P<br />
+.ladder<br />
+</p>
+</li>
+</ul>
+</div>
+<br /><br />
+</html>
+<h2>07/26/12</h2><br />
+•From C0179 (LasR) transformation which grew colonies, we made two liquid cultures: DH5α C0179 LB Cb 100 (two cultures) and a control without bacteria [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Liquid_culture | LIQUID CULTURE]]. <br />
+•We extracted plasmid from 8 C0179 tubes, from 2 tubes of C0179 (Miguel’s transformation), Puc, B.S. control and PSB4AE. <br />
+•Due to problems with the way we did the transformations of ligations we repeated them: <br />
+GusAPCR X,P+ B0079 S,P dephosphorylated<br />
+GusAPCR X,P+ B0079 S,P dephosphorylated (-)<br />
+GusAPCR X,P+ A3 S,P dephosphorylated<br />
+GusAPCR X,P+ A3 S,P dephosphorylated (-)<br />
+[[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Transformation | TRANSFORMATION PROTOCOL]]. <br />
+•Did the following digestions [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Digestion_protocol_.2820_.C2.B5l.29 | LIQUID CULTURE]]. <br />
+•AraC+ Ω+AmyE 3’   S,P 1,2,3,4<br />
+•K143002 X,P<br />
+•AraC+ Ω S,P<br />
+•C0179 X,S<br />
+<h2>07/27/12</h2><br /><br />
+Ligated AraC+ Ω S,P dephosphorylated + K143002 X,P [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Ligation | LIGATION PROTOCOL]]. <br />
+<h2>07/30/12</h2><br /><br />
+•Transformed with ligations: <br />
+•AraC+ Ω  dephosphprylated +K143002 X,P<br />
+•GusAPCR X,P+ A3 S,P dephosphorylated<br />
+•GusAPCR X,P+ B0079 S,P dephosphorylated<br />
+•Transformed the following sythesis: <br />
+•91996 Pveg	140 bp<br />
+•91997 ArsR-CzrA_promoter 1	194 bp<br />
+•91998 ArsR-CzrA_promoter 2	221 bp<br />
+•91999 ArsR-CzrA_promoter 3	213 bp<br />
+•92000 pBad-pXyl			387 bp<br />
+•92001 XylR				1117pb<br />
+•92002 CI_pro_(NAND_INHIBITOR)	774 <br />
+•These synthesis come in pJ209 and supposedly come with Chloramphenicol+ and Gentamicin+ resistance, but we discovered that only Chloramphenicol worked.
+[[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Transformation | TRANSFORMATION PROTOCOL]]. <br />
+•Make liquid cultures of the following transformations for tomorrow [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Liquid_culture | LIQUID CULTURE]]: <br />
+•AraC+ Ω+K143002 <br />
+•GusA+A3<br />
+•GusA+B0079<br />
+•Synthesis<br />
+<h2>07/31/12</h2><br /><br />
+Extracted plasmids from yesterday’s cultures and from K143002 cultures that were in the other lab. <br />
+<br />
+<br />
+::::::::::::::::::::::::::::::::::::::[[File:UnamgenomcisUp.png|right | 120px |link=Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#Arabinose.2FXylose_AND_Gate_Notebook]]
+=AUGUST=
+<h2>08/01/12</h2><br /><br />
+Digested XylR 01 X,P; pBAD-pXyl X,P; Pveg 96 S,P [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Digestion_protocol_.2820_.C2.B5l.29 | LIQUID CULTURE]]. <br /><br />
+<html>
+<div class='thumbnailWrapper'>
+<ul>
+<li>
+<img src='https://static.igem.org/mediawiki/2012/b/b1/UnamgenomicsandsugarBitacora_17.1.jpg' height="300"/>
+<div class='captiongray'>
+<p class='captionInside'>1 PCR GusA I<br />
+PCR GusA I<br />
+PCR GusA P<br />
+PCR GusA P<br />
+ladder 1 Kb<br /></p>
+</li>
+</ul>
+</div>
+<br /><br />
+</html>
+<h2>08/02/12</h2><br /><br />
+•Extracted plasmids from liquid cultures: <br />
+AraC+ Ω+K143002 <br />
+•GusA+A3<br />
+•GusA+BBR1<br />
+PCR GusA, GusA I, PCR GusA P, PCR GusA I<br />
+•Add 10 μl  of each primer (LW and UP). <br />
+•Add 3 μl  of plasmid (P). <br />
+•Add 30.4 μl   buffer. <br />
+•Add 5 μl   Mg. <br />
+•Add 8 μl   DNTp’s. <br />
+•Add 42.6μl   H2O miliQ. <br />
+•Add 1 μl   RTTG polymerase. <br />
+•Centrifuge (spin) 8 secs. <br />
+•Add mineral oil till the eppendorf is full. <br />
+•Place eppendorf 1 mL in thermocycler. <br />
+•Run PCR with program “BERNA”. <br />
+<br />
+<br />
+<br />
+<html>
+<div class='thumbnailWrapper'>
+<ul>
+<li>
+<img src='https://static.igem.org/mediawiki/2012/8/82/UnamgenomicsandsugarBitacora_18.jpg' height="300"/>
+<div class='captionnaranja'>
+<p class='captionInside'>1.GusA PCR 1<br />
+.GusA PCR 2<br />
+.A3+GusA 1<br />
+.A3+GusA 2<br />
+.A3+GusA 3<br />
+.P GusA<br />
+.P GusA 2<br />
+.Ladder<br />
+.01<br />
+.06<br />
+.96<br />
+</p>
+</li>
+</ul>
+</div>
+<br /><br />
+</html>
+<br />
+<br />
+<h2>08/03/12</h2><br /><br />
+• Ran a gel with: (18) <br />
+[[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Gel_electrophoresis | GEL ELECTROPHORESIS PROTOCOL]] . <br />
+•Ran another gel to extract with: <br />
+.GusA PCR 1<br />
+.GusA PCR 2<br />
+.00<br />
+.01<br />
+[[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Gel_electrophoresis | GEL ELECTROPHORESIS PROTOCOL]] . <br />
+•Did the following digestions [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Digestion_protocol_.2820_.C2.B5l.29 | LIQUID CULTURE]]: <br />
+• Ω+K143002  E,X; A3+GusA E,S; GusAPCR X,P <br />
+•Extracted GusAPCR X,P  digestion [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Gel_extraction_protocol | LIQUID CULTURE]]. <br />
+•Left the following ligation: AraC+ Ω+K143002  [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Ligation | LIGATION PROTOCOL]]. <br /><br />
+<br />
+<br />
+<br />
+<html>
+<div class='thumbnailWrapper'>
+<ul>
+<li>
+<img src='https://static.igem.org/mediawiki/2012/1/17/UnamgenomicsandsugarBitacora_19.jpg' height="300"/>
+<div class='captionrojo'>
+<p class='captionInside'>1.A3+GusA 2<br />
+.A3+GusA 3<br />
+. Ω+AmyE 3’ 2<br />
+. Ω+AmyE 3’ 3<br />
+.XylR X,P<br />
+.pBad-pXyl X,P<br />
+.GusA PCR X,P<br />
+</p>
+</li>
+</ul>
+</div>
+<br /><br />
+</html>
+<h2>08/06/12</h2><br /><br />
+•Made liquid cultures of  Ω+K143002   (2 cultures+1 control) and AraC+ Ω+K143002  (2 cultures+1 control) [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Liquid_culture | LIQUID CULTURE]]. <br />
+•Ligated GusAPCR X,P+B0079 S,P dephosphorylated [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Ligation | LIGATION PROTOCOL]]. <br />
+•Ran a Gel with: (19) <br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<html>
+<div class='thumbnailWrapper'>
+<ul>
+<li>
+<img src='https://static.igem.org/mediawiki/2012/8/8b/UnamgenomicsandsugarBitacora_19.1.jpg' height="300"/>
+<div class='captionverde'>
+<p class='captionInside'>Digested 14 tubes of AraC+ Ω+AmyE 3’  E,P <br />
+</p>
+</li>
+</ul>
+</div>
+<br /><br />
+</html>
+<h2>08/08/12</h2><br />
+BBa_B0040 	6I	psB1A2	Amp+		plate 1<br />
+Digested 14 tubes of AraC+ Ω+AmyE 3’  E,P [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Digestion_protocol_.2820_.C2.B5l.29 | LIQUID CULTURE]]. (19.1) <br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<h2>08/09/12</h2><br />
+•From yesterday’s PCR’s : <br />
+• E0040 plasmid 1<br />
+E0040 plasmid 2<br />
+E0040 digested 1<br />
+E0040 digested 2<br />
+We purified with PCR kit<br />
+•Ran  a gel [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Gel_electrophoresis | GEL ELECTROPHORESIS PROTOCOL]] . <br />
+•Made 14 PCR’s from AraC+ Ω+AmyE 3’. <br />
+•From B0079+GusA ligation and B0040 transformation:
+•Grew colonies. <br />
+•Made liquid cultures [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Liquid_culture | LIQUID CULTURE]]. <br />
+•Streaked these in a new plate. <br />
+•Diluted plasmid E0080 2 1/50. <br />
+<br />
+<br />
+<h2>08/10/12</h2><br />
+•Yesterday’s gel did not come out as expected so we repeated the PCR. <br />
+<br />
+<br />
+<html>
+<div class='thumbnailWrapper'>
+<ul>
+<li>
+<img src='https://static.igem.org/mediawiki/2012/e/ef/UnamgenomicsandsugarBitacora_20.jpg' height="300"/>
+<div class='captionrosa'>
+<p class='captionInside'>1.AraC+ Ω+AmyE 3’  <br />
+-14.AraC+ Ω+AmyE 3’  <br />
+.AraC+ Ω 1<br />
+.AraC+ Ω 1<br />
+.AraC+ Ω 1<br />
+.PCR 1 GFP<br />
+.PCR GFP<br />
+</p>
+</li>
+</ul>
+</div>
+<br /><br />
+</html>
+<br />
+<h2>08/13/12</h2><br />
+•After running a gel with 14 PCR’s AraC+ Ω+AmyE 3’  and it did not come out as expected, we ran a gel with the ligation AraC+ Ω+AmyE 3’ to select candidate (that weight the same as the ligation) [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Gel_electrophoresis | GEL ELECTROPHORESIS PROTOCOL]] : (20) <br />
+•Extracted pasmids form liquid cultures: B0049, B0079+GusA. <br />
+•AraC+ Ω+AmyE 3’  undigested didn’t run in the gel as expected, it ran similarly to AraC+ Ω<br />
+• We repeated the ligation AraC+ Ω S,P dephosphorylated+K143002 X,P [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Ligation | LIGATION PROTOCOL]]. <br />
+•	GFP PCR gel came out with two bands one is GFP and the other one are the primers, even after purifying by kit. We joined 2 GFP PCR tubes.
+•	We ran a gel to extract. <br />
+<br />
+<br />
+<br />
+<html>
+<div class='thumbnailWrapper'>
+<ul>
+<li>
+<img src='https://static.igem.org/mediawiki/2012/f/f1/UnamgenomicsandsugarBitacora_22.jpg' height="300"/>
+<div class='captionaqua'>
+<p class='captionInside'>1.6 AraC+ Ω+AmyE 3’  E  with P. <br /><br />
+.8 AraC+ Ω+AmyE 3’  E  with P. <br />
+.11 AraC+ Ω+AmyE 3’  E  with P. <br />
+.12 AraC+ Ω+AmyE 3’  E  with P. <br />
+.6 AraC+ Ω+AmyE 3’  with E,X. <br />
+.8 AraC+ Ω+AmyE 3’  with E,X. <br />
+.11 AraC+ Ω+AmyE 3’  with E,X. <br />
+.12 AraC+ Ω+AmyE 3’  with E,X. <br />
+.00 pBad/pXyl with S,P. <br />
+.Ladder. <br />
+.E0040 PCR E,S to extract the correct band. <br />
+</p>
+</li>
+</ul>
+</div>
+<br /><br />
+</html>
+<h2>08/16/12</h2><br />
+•Ran a gel with yesterday’s digestions: <br />
+•Digested: <br />
+ArSR-CzrA 97 with S,P<br />
+ArSR-CzrA 98 with S,P<br />
+ArSR-CzrA 99 with S,P<br />
+E0040 PCR with E,S<br />
+[[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Digestion_protocol_.2820_.C2.B5l.29 | Digestion Protocol]]. <br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<h2>08/20/12</h2><br />
+•Ligated B0079 S,P dephosphorylated + GusA PCR X,P and pVeg S,P dephosphorylated + XylR X,P [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Ligation | LIGATION PROTOCOL]]. <br />
+<h2>08/21/12</h2><br />
+•Joined both .6 ml tubes of B0014 EX and B0014 XE in one and dephosphorylated. <br />
+•Extracted plasmid from the 24 tubes of of ligation K143001+pBad/pXylR. <br />
+•Digested  Ω+AmyE 3’  with E,X and + Ω+AmyE 3’  II with E,X (obtained these two from glycerols stored at -80ºC [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Digestion_protocol_.2820_.C2.B5l.29 | LIQUID CULTURE]]. <br />
+<html>
+<div class='thumbnailWrapper'>
+<ul>
+<li>
+<img src='https://static.igem.org/mediawiki/2012/2/29/UnamgenomicsandsugarBitacora_22.1.jpg' height="300"/>
+<div class='captionmoradoclaro'>
+<p class='captionInside'>Digested K143001+PBad, pXyl with E,S <br />
+</p>
+</li>
+</ul>
+</div>
+<br /><br />
+</html>
+<html>
+<div class='thumbnailWrapper'>
+<ul>
+<li>
+<img src='https://static.igem.org/mediawiki/2012/1/1c/UnamgenomicsandsugarBitacora_23.jpg' height="300"/>
+<div class='captionmorado'>
+<p class='captionInside'>1.K143001+PBad, pXyl  E,S 10<br />
+.K143001+PBad, pXyl  E,S 11<br />
+.K143001+PBad, pXyl  E,S 12<br />
+.A3 PCR<br />
+.A3 PCR<br />
+.E0040 PCR E,S<br />
+.B0014 E,X dephosphorylated<br />
+. Ω+AmyE 3’  E,X <br />
+. Ω+AmyE 3’  E,X II<br />
+.Ladder
+</p>
+</li>
+</ul>
+</div>
+<br /><br />
+</html>
+<h2>08/22/12</h2><br />
+•We did 2 PCR’s for A3. <br />
+•Digested K143001+PBad, pXyl with E,S <br /> [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Digestion_protocol_.2820_.C2.B5l.29 | LIQUID CULTURE]]. (22.1) <br />
+[[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Gel_electrophoresis | GEL ELECTROPHORESIS PROTOCOL]] . <br />
+•Did band extraction of: <br />
+. K143001+PBad, pXyl  E,S 10<br />
+.K143001+PBad, pXyl  E,S 11<br />
+.K143001+PBad, pXyl  E,S 12<br />
+[[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Gel_extraction_protocol | LIQUID CULTURE]]. <br />
+•Made liquid cultures from E1010+Boo14 that the other lab gave us and did 2 plates for glycerol Km+ [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Liquid_culture | LIQUID CULTURE]] <br /> [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#GLYCEROL_PROTOCOL | GLYCEROL PROTOCOL]] . <br />
+•Did 2 plates for glycerol of both K143001+pBad/pXyl 10y11 Km+ and AraC+ Ω+AmyE 3’  6,8,11,12 Km+ and Spectinomycin+ [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#GLYCEROL_PROTOCOL | GLYCEROL PROTOCOL]] . <br />
+•Transformed ligations: <br />
+B0079+GusA Amp+<br />
+Pveg+XylR Chloramphenicol+
+[[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Transformation | TRANSFORMATION PROTOCOL]].. <br />
+<br />
+<br />
+<html>
+<div class='thumbnailWrapper'>
+<ul>
+<li>
+<img src='https://static.igem.org/mediawiki/2012/7/78/UnamgenomicsandsugarBitacora_23.01.jpg' height="300"/>
+<div class='captionazul'>
+<p class='captionInside'>1. Ω+AmyE 3’  E,X 6.2<br />
+.Ω+AmyE 3’  II E,X<br />
+.97 ArsR-CzrA<br />
+.98 ArsR-CzrA<br />
+.99 ArsR-CzrA
+</p>
+</li>
+</ul>
+</div>
+<br /><br />
+</html>
+<h2>08/23/12</h2><br />
+•The negative controls were contaminated. We didn’t manipulate the ones that had grown because of this. <br />
+•Ran gel with [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Gel_electrophoresis | GEL ELECTROPHORESIS PROTOCOL]] : (23.01) <br />
+[[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Digestion_protocol_.2820_.C2.B5l.29 | Digestion Protocol]]. <br />
+<h2>08/24/12</h2><br />
+From plate with ligation E0040+B0014, ligation K143001+pBad,pXyl 10 and 11, and ligation AraC+ Ω+AmyE 3’  6 and 8  we streaked 2 plates for glycerol of each ligation. <br />Repeated ligation B0079+GusA. <br />
+Ligated E0040 PCR E,S+B0014 E,X dephospohylated [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Ligation | LIGATION PROTOCOL]]. <br />
+Made 2 new plates from Pveg+XylR ligation and liquid cultures [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Liquid_culture | LIQUID CULTURE]]. <br />
+<h2>08/25/12</h2><br />
+Extracted pellet from 16 tubes of pVeg+XylR that were left overnight. <br />
+Ligated B0079+GusA and B0040+B0014 [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Ligation | LIGATION PROTOCOL]]. <br />
+<h2>08/28/12</h2><br />
+Made liquid cultures from transformations tht were left overnight
+-R0079+GusA<br />
+-R0079+GusA (-)<br />
+-E0040+B0014<br />
+-E0040+B0014 (-)<br />
+[[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Liquid_culture | LIQUID CULTURE]]. <br />
+<html>
+<div class='thumbnailWrapper'>
+<ul>
+<li>
+<img src='https://static.igem.org/mediawiki/2012/2/25/UnamgenomicsandsugarBitacora_23.1.jpg' height="300"/>
+<div class='captiongray'>
+<p class='captionInside'>1. A3 PCR 1. <br />
+. A3 PCR 2. <br />
+. Ω+AmyE 3’   S,P *.<br />
+. Ω+AmyE 3’   S,P . <br />
+. Pveg+XylR E,S 2. <br />
+. Pveg+XylR E,S 3. <br />
+. Pveg+XylR E,S 4. <br />
+</p>
+</li>
+</ul>
+</div>
+<br /><br />
+</html>
+<h2>08/29/12</h2><br />
+Digested Pveg+XylR 2,3,4 with E,S. <br />
+Digested  Ω+AmyE 3’   with S,P [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Digestion_protocol_.2820_.C2.B5l.29 | DIGESTION]]. <br />
+Ran a PCR with A3 PCR (2 .6 ml tubes). <br />
+Ran a gel with <br /> [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Gel_electrophoresis | GEL ELECTROPHORESIS PROTOCOL]] : (23.01) <br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<html>
+<div class='thumbnailWrapper'>
+<ul>
+<li>
+<img src='https://static.igem.org/mediawiki/2012/2/2e/UnamgenomicsandsugarBitacoraBitacora_24.jpg' height="300"/>
+<div class='captiongray'>
+<p class='captionInside'>1-23.	E0040 + B0014 colonies<br />
+-29.	B0079+GusA 1<br />
+.	B0079<br />
+</p>
+</li>
+</ul>
+</div>
+<br /><br />
+</html>
+<h2>08/30/12</h2><br />
+•Ran a gel [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Gel_electrophoresis | GEL ELECTROPHORESIS PROTOCOL]] : (24) <br />
+•Digested PVeg+XylR 1,5,7,10,13,16 with E,S; E0040+B0014 3,4,5,10,11,19,21,22 with X,P; B0079+GusA 3,4,5 E,S [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Digestion_protocol_.2820_.C2.B5l.29 | LIQUID CULTURE]]. <br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<html>
+<div class='thumbnailWrapper'>
+<ul>
+<li>
+<img src='https://static.igem.org/mediawiki/2012/3/3d/UnamgenomicsandsugarBitacora_25.jpg' height="300"/>
+<div class='captionnaranja'>
+<p class='captionInside'>1-3B0079+GusA E,S 3. <br />
+-9. PVeg+XylR  E,S 1. <br />
+-17. E0040+B0014 X,P 3. <br />
+. 1 kb ladder. <br />
+</p>
+</li>
+</ul>
+</div>
+<br /><br />
+</html>
+<html>
+<div class='thumbnailWrapper'>
+<ul>
+<li>
+<img src='https://static.igem.org/mediawiki/2012/d/d2/UnamgenomicsandsugarBitacora_26.jpg' height="300"/>
+<div class='captionrojo'>
+<p class='captionInside'>1.A3 PCR. <br />
+</p>
+</li>
+</ul>
+</div>
+<br /><br />
+</html>
+<html>
+<div class='thumbnailWrapper'>
+<ul>
+<li>
+<img src='https://static.igem.org/mediawiki/2012/7/7b/UnamgenomicsandsugarBitacora_27.jpg' height="300"/>
+<div class='captionverde'>
+<p class='captionInside'>E0040+B0014 X,P 4 to extract<br />
+</p>
+</li>
+</ul>
+</div>
+<br /><br />
+</html>
+<h2>08/31/12</h2><br />
+•Ran a gel [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Gel_electrophoresis | GEL ELECTROPHORESIS PROTOCOL]] : (25) <br />
+•Dephosphorylated: <br />
+Ω+AmyE 3’  S,P <br />
+Ω+AmyE 3’  II S,P <br />
+AraC+ Ω+AmyE 3’  E,X<br />
+AraC+ Ω+AmyE 3’  E,X<br />
+AraC+ Ω+AmyE 3’  E,X<br />
+AraC+ Ω+AmyE 3’  E,X<br /><br />•Ran a gel with A3 PCR [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Gel_electrophoresis | GEL ELECTROPHORESIS PROTOCOL]] : (26) <br />
+•It was the second time we didn’t obtain a band from A3’s PCR.
+•Probably because it had been missing the buffer 2’s ethanol (“blue lid”) from the PCR purification. <br />
+•Ran a gel woth E0040+B0014 X,P 4 to extract <br /> [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Gel_extraction_protocol | Gen extraction protocol]]. <br />
+•Did an A3 PCR. <br />
+<br />
+<br />
+<br />
+<br />
+<br />
+::::::::::::::::::::::::::::::::::::::[[File:UnamgenomcisUp.png|right | 120px |link=Team:UNAM_Genomics_Mexico/Notebook/ANDSugar#Arabinose.2FXylose_AND_Gate_Notebook]]
+=SEPTEMBER=
+<html>
+<div class='thumbnailWrapper'>
+<ul>
+<li>
+<img src='https://static.igem.org/mediawiki/2012/b/b8/UnamgenomicsandsugarBitacora_28.jpg' height="300"/>
+<div class='captionrosa'>
+<p class='captionInside'>1.A3 PCR 1. <br />
+.A3 PCR 2. <br />
+.E0040+B0014 X,P 1. <br />
+.E0040+B0014 X,P 2. <br />
+.Ω+AmyE 3’  dephosphorylated S,P. <br />
+.Ω+AmyE 3’  dephosphorylated S,P II. <br />
+.97 dephosphorylated S,P. <br />
+.98 dephosphorylated S,P. <br />
+.99 dephosphorylated S,P. <br />
+-13.	Arac+ Ω+AmyE 3’  dephosphorylated  E,X 12. <br />
+.	1 kb Ladder. <br />
+</p>
+</li>
+</ul>
+</div>
+<br /><br />
+</html>
+<h2>09/01/12</h2><br />
+•Ran a gel with [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Gel_electrophoresis | GEL ELECTROPHORESIS PROTOCOL]] : (28) <br />
+•Ligated E0040+B0014 X,P 2 +promoter S,P dephosphorylated; K143002 X,P+ Ω+AmyE 3’  dephosphorylated S,P [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Ligation | LIGATION PROTOCOL]]. <br />
+<br />
+<br />
+<br />
+<br />
+<h2>09/03/12</h2><br />
+•Digested B0079+GusA E,S 3,4,5; PVeg+XylR E,S 1,5,7,10,13,16 [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Digestion_protocol_.2820_.C2.B5l.29 | LIQUID CULTURE]]. <br />
+<h2>09/04/12</h2><br />
+•Ran gel with digestions: <br />
+B0079+GusA E,S 3,4,5<br />
+PVeg+XylR E,S 1,5,7,10,13,16 <br />
+[[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Gel_electrophoresis | GEL ELECTROPHORESIS PROTOCOL]] . <br />
+•Purified A3 PCR 1,2. <br />
+•Ran a gel of A3 PCR <br /> [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Gel_electrophoresis | GEL ELECTROPHORESIS PROTOCOL]]  and digested with X,P [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Digestion_protocol_.2820_.C2.B5l.29 | LIQUID CULTURE]]. <br />
+•From ligations: PVeg+E0040+B0014, PBad/PXyl+E0040+B0014, B0079+E0040+B0014 only colonies grew in PBad/PXyl+E0040+B0014.
+•Plated colonies that grew in a new plate. <br />
+•Made liquid cultures of these <br /> [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Liquid_culture | LIQUID CULTURE]]. <br />
+•Repeated the ones that did not grow. <br />
+•Digested E0040+B0014 4 with X,P[[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Digestion_protocol_.2820_.C2.B5l.29 | LIQUID CULTURE]]. <br />
+•Ran a gel [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Gel_electrophoresis | GEL ELECTROPHORESIS PROTOCOL]] . <br />
+•Extracted from gel [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Gel_extraction_protocol | LIQUID CULTURE]]. <br />
+-BBa_J23101	18E	plate 1	plasmid BBa_J61002_2948 bp 	Amp+<br />
+<html>
+<div class='thumbnailWrapper'>
+<ul>
+<li>
+<img src='https://static.igem.org/mediawiki/2012/c/c1/UnamgenomicsandsugarBitacora_29.jpg' height="300"/>
+<div class='captionaqua'>
+<p class='captionInside'>24 PBad/PXyl+E0040+B0014 tubes we extracted <br />
+</p>
+</li>
+</ul>
+</div>
+<br /><br />
+</html>
+<html>
+<div class='thumbnailWrapper'>
+<ul>
+<li>
+<img src='https://static.igem.org/mediawiki/2012/a/a4/UnamgenomicsandsugarBitacora_30.jpg' height="300"/>
+<div class='captionmoradoclaro'>
+<p class='captionInside'>1.E0040+B0014 X,P<br />
+.E0040+B0014 X,P<br />
+.PVeg+XylR E<br />
+.B0079+GusA S<br />
+.1 kb plus ladder<br />
+Extracted band from 1. and 2
+<br />
+</p>
+</li>
+</ul>
+</div>
+<br /><br />
+</html>
+<html>
+<div class='thumbnailWrapper'>
+<ul>
+<li>
+<img src='https://static.igem.org/mediawiki/2012/7/7d/UnamgenomicsandsugarBitacora_31.jpg' height="300"/>
+<div class='captionmorado'>
+<p class='captionInside'>Digested B0079+GusA with E,S 4,5; PVeg+XylR with E,S
+<br />
+</p>
+</li>
+</ul>
+</div>
+<br /><br />
+</html>
+<h2>09/05/12</h2><br />
+•From the 24 PBad/PXyl+E0040+B0014 tubes we extracted plasmids  (29)  and ran a gel [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Gel_extraction_protocol | LIQUID CULTURE]]. <br />
+•Extracted plasmid from 2 tubes of E0040+B0014. <br />
+•Ran a gel with yesterday’s digestions: <br />
+.E0040+B0014 X,P<br />
+.E0040+B0014 X,P<br />
+.PVeg+XylR E<br />
+.B0079+GusA S<br />
+.1 kb plus ladder<br />
+•Extracted band from 1. and 2. [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Gel_extraction_protocol | LIQUID CULTURE]]. <br />
+•Purified A3 PCR from 2 0.6ml tubes 1 and 2. <br />
+•1 colony grew from ligation pVeg+E0040+B0014. <br />
+•We streaked this in another plate and did liquid cultures <br /> [[Team:UNAM_Genomics_Mexico/Notebook/Protocols#Liquid_culture | LIQUID CULTURE]]. <br />
+•To do: <br />
+•Ligate B0079 S,P dephosphorylated + E0040+B0014 X,P and  Ω+AmyE 3’   S,P dephosphorylated+ K143001 X,P. <br />
+•Digested B0079+GusA with E,S 4,5; PVeg+XylR with E,S 10,13. (31) <br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<html>
+<div class='thumbnailWrapper'>
+<ul>
+<li>
+<img src='https://static.igem.org/mediawiki/2012/2/26/UnamgenomicsandsugarBitacora_32.jpg' height="300"/>
+<div class='captionazul'>
+<p class='captionInside'>•A3 PCR and gel A3 PCR X,P
+<br />
+</p>
+</li>
+</ul>
+</div>
+<br /><br />
+</html>
+<br />
+<h2>09/06/12</h2><br />
+•A3 PCR and gel A3 PCR X,P 1,2. <br />
+<h2>09/14/12</h2><br />
+•Digested  Ω+AmyE 3’  11,13,18, and 22 with E,X. <br />
+•Ligate: <br />
+PVeg S,P dephosphorylated+XylR X,P. <br />
+PBad p Xyl S,P dephosphorylated + E0040+B0014 X,P. <br />
+pSB13C3 E,P dephosphorylated + A3 PCR E,P. <br />
+pSB13C3 E,P dephosphorylated + GusA PCR E,P. <br />
+pSB13C3 E,P dephosphorylated + XylR E,P. <br />
+pSB13C3 E,P dephosphorylated + pVeg E,P. <br />
+pSB13C3 E,P dephosphorylated + pBad pXyl E,P. <br />
+pSB13C3 E,P dephosphorylated +  Ω PCR E,P. <br />
+<br />
+<br />
+<br />
+<br />
+<br />
+<h2>09/16/12</h2><br />
+•	Colonies in these plates grew: <br />
+-	R0079+E0040+B0014 <br />
+-	pBad/pXyl <br />
+-	XylR <br />
+-	pVeg <br />
+-	A3+E0040+B0014 from colonies 1,3,4,5,6,7,8,9,10,11,12,13,14,15,17 <br />
+-	pVeg+E0040+B0014 1,2,3,4,5,6,8,9,10,11,12,13,14,15,16 <br />
+-	pBad/pXyl+E0040+B0014 2 tubes from the same correct colony. <br />
+-	pVeg+XylR 1,2 <br />
+-	pBad/pXyl+pSB1C3 1,2 <br />
+-	XylR+pSB1C3 1,2 <br />
+-	pVeg+pSB1C3 1,2 <br />
+-	A3+pSB1C3 1,2 <br />
+-	GusA+pSB1C3 1,2 <br />
+-	omegacassette+pSB1C3 1,2 <br />
+<br />
+•	Ran gel from the plasmid extractions that we did yesterday: <br />
+-	A3+E0040+B0014 1-16 <br />
+-	pVeg+E0040+B0014 1-16, 18 <br />
+-	omega cassette+AmyE 3’ 11,13,18,22 <br />
+•	Digested R0079+E0040+B0014 with E,S. to ligate with AmyE 3’ E,x dephosphorylated. <br />
+•	Digested omega cassette with E,P. <br />
+•	Digested pSB1C3 with E,P. <br />
+•	Made liquid cultures from AmyE 5’ and AmyE 3’. <br />
+•	Did plasmid extraction from pSB1C3 colonies 3 and 6. <br />
+<br />
+<h2>09/17/12</h2><br />
+•	Digested A3+E0040+B0014 colonies 2,3,4,5,6,11 and 16 with E,S. <br />
+•	Digested pVeg+E0040+B0014 colonies 1,2,3,4,5,9 and 10 with E,S. <br />
+•	Dephosphorylated omega cassette+AmyE 3’ colonies 13,18 and 22 digested with E,X. <br />
+•	Digested pBad/pXyl and pVeg with S,P. Then dephosphorylated. <br />
+•	Digested AmyE 3’ with E,X. Then dephosphorylated. <br />
+<br />
+<h2>09/18/12</h2><br />
+<br />
+•	Ran gel with: <br />
+.	A3 2 E,S <br />
+.	A3 3 E,S <br />
+.	A3 4 E,S <br />
+.	A3 5 E,S <br />
+.	A3 6 E,S <br />
+.	A3 11 E,S <br />
+.	A3 16 E,S <br />
+.	E0040+B0014 colony 1 E,X <br />
+.	AmyE 5’ E,P <br />
+.	AmyE 3’ E,X <br />
+.	Omega cassette E,S <br />
+.	pSB1C3 E,P <br />
+.	ladder <br />
+Bottom: <br />
+.	pVeg 1 E,S <br />
+.	pVeg 2 E,S <br />
+.	pVeg 3 E,S <br />
+.	pVeg 4 E,S <br />
+.	pVeg 5 E,S <br />
+.	pVeg 9 E,S <br />
+.	pVeg 10 E,S <br />
+.	pVeg S,P dephosphorylated <br />
+.	pVeg 2 S,P <br />
+.	pBad/pXyl S,P <br />
+.	XylR X,P <br />
+.	R0079+GFP+TT E,S <br />
+.	R0079 S,P <br />
+.	Ladder <br />
+•	Dephosphorylated GFP+TT E,X; AmyE 5’ E,X; pSB1C3 E,P; pVeg 2 S,P; pBad/pXyl S,P and R0079 S,P. <br />
+<br />
+<h2>09/19/12</h2><br />
+<br />
+•	Did PCR from A3 and a 1/50 dilution. <br />
+•	Ran gel with: <br />
+.	pVeg 3 E,P. <br />
+.	pVeg 9 E,P. <br />
+.	pVeg 10 E,P. <br />
+.	pBAd/pXyl 3 E,P. <br />
+.	pBAd/pXyl 5 E,P. <br />
+.	pBAd/pXyl 1 E,P. <br />
+.	A3 3 E,P. <br />
+.	A3 4 E,P. <br />
+.	XylR 1 E,P. <br />
+.	XylR 3 E,P. <br />
+.	XylR 8 E,P. <br />
+.	pSB1C3 6 E,P. <br />
+.	pSB1C3 6 E,P. <br />
+.	AmyE 5’ E,S. <br />
+.	AmyE 5’ E,S. <br />
+.	A3 1/50 PCR. <br />
+.	A3 PCR. <br />
+.	Ladder <br />
+•	We did transformations: <br />
+-	2 of R0079+GusA <br />
+-	R0079+GusA control <br />
+-	2 of A3+pSB1AK3 <br />
+-	A3+pSB1AK3 control <br />
+-	2 of omega cassette+pSB1C3 <br />
+-	2 of GusA+pSB1C3 <br />
+•	 Digested: <br />
+-	pVeg+pSB1C3 <br />
+-	pBad/pXyl+pSB1C3 <br />
+-	XylR+pSB1C3 <br />
+-	A3+pSB1C3 <br />
+With E,P. <br />
+•	Ran gel with these digestions. <br />
+<br />
+<h2>09/19/12</h2><br />
+•	Made liquids cultures from: <br />
+-	Glicerol of AmyE 5’ <br />
+-	Glicerol of AmyE 3’ <br />
+-	pBad/pXyl+pSB1C3 colony 5 <br />
+•	Made liquid cultures from yesterday transformations: <br />
+-	R0079+GusA 2 and control <br />
+-	A3+pSB1AK3 2 and control <br />
+-	Omega cassette+pSB1C3 2 <br />
+-	GusA+pSB1C3 2 <br />
+•	We transformed yesterday ligations: <br />
+-	pBad/pXyl+pSB1C3 <br />
+-	XylR+pSB1C3 <br />
+-	pVeg+pSB1C3 <br />
+-	A3+pSB1C3 <br />
+•	Purified A3 PCR with kit, and then, digested with E,P and E,S. <br />
+•	Ran gel <br />
+<br />
+<h2>09/20/12</h2><br />
+<br />
+•	Made liquid cultures from transformations: <br />
+-	Omega cassette+pSB1C3 colony 7 <br />
+-	2 of GusA+pSB1C3 colony 32 <br />
+-	R0079+GusA colony 12 <br />
+•	Digested A3 1/50 PCR with E,P and E,S. <br />
+•	Made liquid cultures from R0079+E0040+B0014; pBad/pXyl+E0040+B0014; pVeg+E0040+B0014; A3+E0040+B0014. <br />
+•	Ligated: <br />
+-	pBad/pXyl S,P dephosphorylated + E0040+B0014 X,P <br />
+-	pVeg S,P dephosphorylated + E0040+B0014 X,P <br />
+-	A3 PCR E,S + E0040+B0014 E,X dephosphorylated. <br />
+<br />
+<h2>09/21/12</h2><br />
+<br />
+•	Ran gel with: <br />
+.	R0079+GFP+TT 1 <br />
+.	R0079+GFP+TT <br />
+.	pBad/pXyl+pSB1C3 1 <br />
+.	pBad/pXyl+pSB1C3 <br />
+.	omega cassette+psB1C3 1 <br />
+.	omega cassette+psB1C3 <br />
+.	pSB1C3 E,P 1 <br />
+.	pSB1C3 E,P <br />
+.	pSB1C3 E <br />
+.	pSB1C3 P <br />
+.	A3 1/50 PCR E,P <br />
+<br />
+<h2>09/22/12</h2><br />
+•	Ran gel with lysis extractions: <br />
+.	GusA+pSB1C3 1 <br />
+.	GusA+pSB1C3 2 <br />
+.	GusA+pSB1C3 3 <br />
+.	GusA+pSB1C3 4 <br />
+.	GusA+pSB1C3 5 <br />
+.	GusA+pSB1C3 6 <br />
+.	GusA+pSB1C3 7 <br />
+.	GusA+pSB1C3 8 <br />
+.	GusA+pSB1C3 9 <br />
+.	GusA+pSB1C3 10 <br />
+.	GusA+pSB1C3 11 <br />
+.	GusA+pSB1C3 12 <br />
+.	pSB1C3 <br />
+.	A3+E0040+B0014 1 <br />
+.	A3+E0040+B0014 2 <br />
+.	A3+E0040+B0014 3 <br />
+.	A3+E0040+B0014 4 <br />
+.	A3+E0040+B0014 5 <br />
+.	A3+E0040+B0014 6 <br />
+.	A3+E0040+B0014 7 <br />
+.	A3+E0040+B0014 8 <br />
+.	A3+E0040+B0014 9 <br />
+.	pVeg+E0040+B0014 3 <br />
+.	pVeg+E0040+B0014 4 <br />
+.	pVeg+E0040+B0014 5 <br />
+.	pVeg+E0040+B0014 6 <br />
+.	pVeg+E0040+B0014 7 <br />
+.	pVeg+E0040+B0014 8 <br />
+.	pVeg+E0040+B0014 9 <br />
+.	pVeg <br />
+.	pBad/pXyl+E0040+B0014 1 <br />
+.	pBad/pXyl+E0040+B0014 2 <br />
+.	pBad/pXyl+E0040+B0014 3 <br />
+.	pBad/pXyl+E0040+B0014 4 <br />
+.	pBad/pXyl+E0040+B0014 5 <br />
+.	pBad/pXyl+E0040+B0014 6 <br />
+.	pBad/pXyl+E0040+B0014 7 <br />
+.	pBad/pXyl+E0040+B0014 8 <br />
+.	pBad/pXyl+E0040+B0014 9 <br />
+.	pBad/pXyl+E0040+B0014 10 <br />
+.	pBad/pXyl <br />
+.	pVeg+XylR 1 <br />
+.	pVeg+XylR 2 <br />
+.	pVeg+XylR 3 <br />
+.	pVeg+XylR 4 <br />
+.	pVeg+XylR 5 <br />
+.	pVeg+XylR 6 <br />
+.	pVeg+XylR 7 <br />
+.	pVeg+XylR 8 <br />
+.	omega cassette <br />
+<br />
+•	Ran gel with yesterday digestions: <br />
+.	R0079+GFP+TT E,P <br />
+.	R0079+GFP+TT E,P <br />
+.	Omega cassette+pSB1C3 E,P <br />
+.	Omega cassette+pSB1C3 E,P <br />
+.	Ladder <br />
+.	pBad/pXyl+pSB1C3 <br />
+.	pBad/pXyl+pSB1C3 <br />
+.	pSB1C3 6 E,P. <br />
+.	A3 1/50 PCR E,S <br />
+.	pBbak C011 <br />
+.	pBbak C012 <br />
+.	ladder <br />
+<br />
+•	Did pellet from R0079+GusA. <br />
+•	Did plasmid extraction from omega cassette+pSB1C3 colonies 1,4,6 and 7. <br />
+•	Digested them with E,P. <br />
+•	Digested: <br />
+-	GusA+pSB1C3 1,3,4,10 and 11 <br />
+-	A3+E0040+B0014 2,4,7 and 9 <br />
+-	pVeg+E0040+B0014 4,5 and 6 <br />
+-	pBad/pXyl+E0040+B0014 3,7 and 10 <br />
+-	pVeg+XylR 2,4 and 5 <br />
+with E,P. <br />
+•	Made liquid cultures from pVeg+pSB1C3 <br />
+•	Ligated: <br />
+-	XylR E,P + pSB1C3 E,P dephosphorylated. <br />
+-	pVeg E,P + pSB1C3 E,P dephosphorylated. <br />
+-	A3 1/50 PCR E,P + pSB1C3 E,P dephosphorylated. <br />
+-	pBad/pXyl S,P dephosphorylated + E0040+B0014 X,P. <br />
+-	pVeg S,P dephosphorylated + E0040+B0014 X,P. <br />
+-	A3 1/50 PCR E,S + E0040+B0014 E,X dephosphorylated. <br />
+-	pVeg S,P dephosphorylated + XylR X,P. <br />
+<br />
+<h2>09/23/12</h2><br />
+<br />
+•	Ran gel with yesterday digestions: <br />
+.	Omega cassette+pSB1C3 1 E,P <br />
+.	Omega cassette+pSB1C3 4 E,P <br />
+.	Omega cassette+pSB1C3 6 E,P <br />
+.	Omega cassette+pSB1C3 7 E,P <br />
+.	GusA+pSB1C3 1 E,P <br />
+.	GusA+pSB1C3 3 E,P <br />
+.	GusA+pSB1C3 4 E,P <br />
+.	GusA+pSB1C3 10 E,P <br />
+.	GusA+pSB1C3 11 E,P <br />
+.	pSB1C3 E,P dephosphorylated <br />
+.	pVeg+XylR 2 E,P <br />
+.	pVeg+XylR 4 E,P <br />
+.	pVeg+XylR 5 E,P <br />
+.	pVeg S,P dephosphorylated <br />
+.	pVeg+GFP+TT 4 E,P. <br />
+.	pVeg+GFP+TT 5 E,P. <br />
+.	pVeg+GFP+TT 6 E,P. <br />
+.	ladder <br />
+Bottom <br />
+.	pBad/pXyl+GFP+TT 3 E,P <br />
+.	pBad/pXyl+GFP+TT 7 E,P <br />
+.	pBad/pXyl+GFP+TT 10 E,P <br />
+.	pBad/pXyl S,P dephosphorylated <br />
+.	A3+GFP+TT 2 E,P <br />
+.	A3+GFP+TT 4 E,P <br />
+.	A3+GFP+TT 7 E,P <br />
+.	A3+GFP+TT 9 E,P <br />
+.	Ladder <br />
+<br />
+<h2>09/24/12</h2><br />
+<br />
+•	Did PCR from omega cassette+pSB1C3 colonies 1,4,6 and 7. <br />
+•	Made 1/50 dilutions from these PCR products. <br />
+•	Ran gel with: <br />
+.	Omega cassette+pSB1C3 1/50 PCR 1 <br />
+.	Omega cassette+pSB1C3 PCR 1 <br />
+.	Omega cassette+pSB1C3 1/50 PCR 4 <br />
+.	Omega cassette+pSB1C3 PCR 4 <br />
+.	Omega cassette+pSB1C3 1/50 PCR 6 <br />
+.	Omega cassette+pSB1C3 PCR 6 <br />
+.	Omega cassette+pSB1C3 1/50 PCR 7 <br />
+.	Omega cassette+pSB1C3 PCR 7 <br />
+.	GusA+pSB1C3 1 P <br />
+.	GusA+pSB1C3 3 P <br />
+.	GusA+pSB1C3 4 P <br />
+.	GusA+pSB1C3 10 P <br />
+.	GusA+pSB1C3 11 P <br />
+.	pVeg+pSB1C3 6 E,P <br />
+.	pVeg+pSB1C3 5 E,P <br />
+.	pVeg+pSB1C3 4 E,P <br />
+.	pVeg+pSB1C3 3 E,P <br />
+.	pVeg+pSB1C3 2 E,P <br />
+.	pVeg+pSB1C3 1 E,P <br />
+.	ladder <br />
+•	From yesterday transformations, these didn’t grow: <br />
+-	pBad/pXyl+E0040+B0014 1 and 2. <br />
+-	A3+E0040+B0014. <br />
+•	Made liquid cultures from transformations that did grow: <br />
+-	pVeg+E0040+B0014. <br />
+-	pVeg+XylR. <br />
+-	A3+pSB1C3 <br />
+-	pVeg+pSB1C3 <br />
+-	XylR+pSB1C3 <br />
+<br />
+<h2>09/26/12</h2><br />
+<br />
+•	Did plasmid extractions form liquids cultures: <br />
+-	8 of pVeg+pSB1C3 <br />
+-	8 of A3 <br />
+-	8 of XylR <br />
+•	Digested them with E,P. <br />
+•	Ran gel with: <br />
+.	Ladder <br />
+.	XylR+pSB1C3 1 E,P <br />
+.	XylR+pSB1C3 2 E,P <br />
+.	XylR+pSB1C3 3 E,P <br />
+.	pVeg+pSB1C3 1 E,P <br />
+.	pVeg+pSB1C3 3 E,P <br />
+.	pVeg+pSB1C3 4 E,P <br />
+.	pVeg+pSB1C3 5 E,P <br />
+.	pVeg+pSB1C3 6 E,P <br />
+.	pVeg+pSB1C3 8 E,P <br />
+.	pSB1C3 6 E,P dephosphorylated <br />
+.	A3+pSB1C3 1 E,P <br />
+.	A3+pSB1C3 3 E,P <br />
+.	A3+pSB1C3 4 E,P <br />
+.	A3+pSB1C3 5 E,P <br />
+.	A3+pSB1C3 6 E,P <br />
+.	A3+pSB1C3 8 E,P <br />
+.	Ladder <br />
+.	P4+E0040+B0014 1 E,X <br />
+.	P4+E0040+B0014 7 E,X <br />
+<br />
+<h2>09/27/12</h2><br />
+<br />
+•	Digested pVeg+XylR colonies 1,4,5 and 6 in pJ209 plasmid with E,S for 3 hours. <br />
+•	Digested pVeg+E0040+B0014 colonies 7,9,10 and 11 in pasmid pJ209 with E,P. <br />
+<br />
+<h2>10/09/12</h2><br />
+<br />
+•	Ligated: <br />
+-	A3 1/50 PCR E,P + pSB1C3 6 E,P dephosphorylated. <br />
+-	pVeg S,P dephosphorylated + XylR X,P. <br />
+-	P4+CI+E1010+B0014 E,X dephosphorylated + AmyE 5’+pBad/pXyl E,S. <br />
+<br />
+<h2>10/10/12</h2><br />
+<br />
+•	Ligated: <br />
+-	GusA PCR E,P + pSB1C3 6 E,P dephosphorylated. <br />
+-	pBad/pXyl S,P dephosphorylated + E0040+B0014 X,P. <br />
+-	pVeg S,P dephosphorylated + E0040+B0014 X,P. <br />
+-	A3 1/50 PCR E,S + E0040+B0014 E,X dephosphorylated. <br />
+•	Digested R0079+E0040+B0014 with E,S. <br />
+•	Digested AmyE 3’ with E,X. Then dephosphorylated. <br />
+•	Digested pVeg and R0079, A3 with X,P. <br />
+•	Digested pBad/pSB1C3 with S,P. <br />
+<br />
+<h2>10/11/12</h2><br />
+<br />
+•	Did plasmid extraction from liquid cultures: <br />
+-	2 of AmyE 5’ <br />
+-	2 of AmyE 3’ <br />
+-	2 of E0040+B0014 <br />
+•	Ran gel with: <br />
+.	A3 1/50 PCR X,P <br />
+.	A3 1/50 PCR X,P <br />
+.	A3+pSB1C3 6 X,P <br />
+.	A3+pSB1C3 6 X,P <br />
+.	A3+pSB1C3 8 X,P <br />
+.	A3+pSB1C3 8 X,P <br />
+.	pVeg X,P <br />
+.	pVeg 96 X,P <br />
+.	pVeg 96 X,P <br />
+.	pVeg+pSB1C3 1 X,P <br />
+.	pVeg+pSB1C3 1 X,P <br />
+.	pVeg+pSB1C3 3 X,P <br />
+.	pVeg+pSB1C3 3 X,P <br />
+.	R0079 X,P <br />
+.	Ladder <br />
+<br />
+<h2>10/12/12</h2><br />
+<br />
+•	Ligated:
+-	AmyE 5’+pBad/pXyl 10 E,S + P4+CI+E1010+TT E,X dephosphorylated. <br />
+-	AmyE 5’+pBad/pXyl 11 E,S + P4+CI+E1010+TT E,X dephosphorylated. <br />
+-	AmyE 5’+pBad/pXyl 12 E,S + P4+CI+E1010+TT E,X dephosphorylated. <br />
+-	pVeg S,P dephosphorylated + XylR X,P. <br />
+-	A3 1/50 PCR E,P + pSB1C3 E,P dephosphorylated. <br />
+<br />
+<h2>10/12/12</h2><br />
+<br />
+•	Digested AmyE 5’ with S,P <br />
+•	Dephosphorylated it. <br />
+•	Ligated: <br />
+-	AmyE  5’ S,P dephosphorylated with <br />
+-	R0079 X,P <br />
+-	pVeg 96 X,P <br />
+-	A3 1/50 PCR X,P <br />
+-	A3+pSB1C3 6 X,P <br />
+-	R0079+E0040+B0014 <br />
+•	Ligated pBad/pXyl+pSB1C3 S,P dephosphorylated + E0040+B0014 X,P. <br />
+•	Ran gel with: <br />
+.	A3+pSB1C3 1 <br />
+.	A3+pSB1C3 2 <br />
+.	A3+pSB1C3 3 <br />
+.	A3+pSB1C3 4 <br />
+.	A3+pSB1C3 5 <br />
+.	A3+pSB1C3 6 <br />
+.	A3+pSB1C3 7 <br />
+.	A3+pSB1C3 8 <br />
+.	A3+pSB1C3 9 <br />
+.	A3+pSB1C3 10 <br />
+.	A3+pSB1C3 11 <br />
+.	A3+pSB1C3 6 control <br />
+.	AmyE 5’+P4+CI+E1010+B0014 1 <br />
+.	AmyE 5’+P4+CI+E1010+B0014 2 <br />
+.	AmyE 5’+P4+CI+E1010+B0014 3 <br />
+.	AmyE 5’+P4+CI+E1010+B0014 4 <br />
+.	AmyE 5’+P4+CI+E1010+B0014 5 <br />
+.	AmyE 5’+P4+CI+E1010+B0014 6 <br />
+.	AmyE 5’+P4+CI+E1010+B0014 7 <br />
+.	P4+CI+E1010+B0014 1 control <br />
+<br />
+<h2>10/09/12</h2><br />
+<br />
+•	Ligate: <br />
+K143001+pBad/pXyl + p4+CI+E1010+TT E,X dephosphorylated. <br />
+•	Ligate: <br />
+pVeg S,P dephosphorylated + XylR X,P. <br />
+•	Ligate: <br />
+A3 PCR 1/50 E,P + pSB1C3 E,P dephosphorylated <br />
+<br />
+<h2>10/13/12</h2><br />
+<br />
+•	Digested AmyE 5’ with S,P. Then dephosphorylated. <br />
+•	Ligate: <br />
+AmyE 5’ S,P dephosphorylated + <br />
+-	R0079 X,P <br />
+-	pVeg 96 X,P <br />
+-	A3 PCR 1/50 X,P <br />
+-	A3+pSB1C3 colony 6 X,P <br />
+-	R0079+E0040+B0014 E,X <br />
+•	Ligate: <br />
+pBad/pXyl+pSB1C3 S,P dephosphorylated + E0040+B0014 X,P <br />
+•	Ran a gel with: <br />
+.	A3+pSB1C3 1 <br />
+.	A3+pSB1C3 2 <br />
+.	A3+pSB1C3 3 <br />
+.	A3+pSB1C3 4 <br />
+.	A3+pSB1C3 5 <br />
+.	A3+pSB1C3 6 <br />
+.	A3+pSB1C3 7 <br />
+.	A3+pSB1C3 8 <br />
+.	A3+pSB1C3 9 <br />
+.	A3+pSB1C3 10 <br />
+.	A3+pSB1C3 11 <br />
+.	A3+pSB1C3 6 control <br />
+.	AmyE 5’+P4+CI+E1010+B0014 8 <br />
+.	AmyE 5’+P4+CI+E1010+B0014 9 <br />
+.	AmyE 5’+P4+CI+E1010+B0014 10 <br />
+.	P4+CI+E1010+B0014 1 control <br />
+.	pVeg+XylR 1 <br />
+.	pVeg+XylR 2 <br />
+.	pVeg+XylR 3 <br />
+.	pVeg+XylR 4 <br />
+.	pVeg+XylR 5 <br />
+.	pVeg+XylR 6 <br />
+.	pVeg+XylR 7 <br />
+.	pVeg+XylR 8 <br />
+.	pVeg+XylR 10 <br />
+.	pVeg+XylR 11 <br />
+.	pVeg+XylR 12 <br />
+.	pVeg 96 control <br />
+•	Ran gel with: <br />
+.	A3 1/50 PCR X,P <br />
+.	A3+pSB1C3 6 X,P <br />
+.	pVeg 96 X,P <br />
+.	pVeg+pSB1C3 1 X,P <br />
+.	pVeg+pSB1C3 3 X,P <br />
+.	R0079 X,P <br />
+.	pBad/pXyl+pSB1C3 S,P dephosphorylated <br />
+.	ladder <br />
+.	Digested: <br />
+-	A3+pSB1C3 colonies 3,4,5 and 10 with E,P. <br />
+-	 AmyE 5’+pBad/pXyl+P4+CI+E1010*B0014 colonies 1,2,7 and 8 with E,P. <br />
+-	pVeg+XylR 1,4,5 and 12 with E,P. <br />
+•	Ran gel with: <br />
+.	GFP+TT 1 X,P <br />
+.	GFP+TT 1 X,P <br />
+.	GFP+TT 1 E,S <br />
+.	GFP+TT 1 E,S <br />
+.	GFP+TT 2 X,P <br />
+.	GFP+TT 2 X,P <br />
+.	GFP+TT 2 E,S <br />
+.	GFP+TT 2 E,S <br />
+.	Ladder  <br />
+.	A3 1/50 PCR X,P <br />
+.	A3+pSB1C3 6 X,P <br />
+.	pVeg 96 X,P <br />
+.	pVeg+pSB1C3 1 X,P <br />
+.	R0079 X,P <br />
+.	AmyE 5’ S,P <br />
+<h2>10/16/12</h2><br />
+•	Made liquid cultures from yesterday transformations: <br />
+-	AmyE 5’+R0079 <br />
+-	AmyE 5’+R0079_2 <br />
+-	AmyE 5’+A3 <br />
+-	AmyE 5’+pVeg <br />
+-	pBad/pXyl+E0040+B0014 in pSB1C3 plasmid. <br />
+•	Digested: <br />
+-	AmyE 5’+pBad/pXyl+P4+CI+E1010+B0014 colonies 1,2,7 and 8 with E,P. <br />
+-	pVeg+XylR 1,4,5 and 12 with E,P. <br />
+-	R0079+GFP+TT and R0079+GFP+TT_2 with X,P. <br />
 }}

Team:UNAM Genomics Mexico/Notebook/ANDSugar

From 2012.igem.org

Latest revision as of 03:52, 27 October 2012

Arabinose/Xylose AND Gate Notebook

JUNE

06/07/12

06/12/12

06/13/12

06/14/12

06/15/12

06/18/12

06/19/12

06/22/12

06/25/12

06/26/12

06/27/12

06/29/12

JULY

07/03/12

07/04/12

07/06/12

07/07/12

07/08/12

07/09/12

07/10/12

07/11/12

07/12/12

07/13/12

07/14/12

07/16/12

07/17/12

07/18/12

07/19/12

07/20/12

07/23/12

07/24/12

07/25/12

07/26/12

07/27/12

07/30/12

07/31/12

AUGUST

08/01/12

08/02/12

08/03/12

08/06/12

08/08/12

08/09/12

08/10/12

08/13/12

08/16/12

08/20/12

08/21/12

08/22/12

08/23/12

08/24/12

08/25/12

08/28/12

08/29/12

08/30/12

08/31/12

SEPTEMBER

09/01/12

09/03/12

09/04/12

09/05/12

09/06/12

09/14/12

09/16/12

09/17/12

09/18/12

09/19/12

09/19/12

09/20/12

09/21/12

09/22/12

09/23/12

09/24/12

09/26/12

09/27/12