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Revision as of 22:20, 25 September 2012

Week 1

[all]

09.07. - 15.07.2012

09.07.2012

Inoculation: E. coli strain C600 Mucts 62' in DYT-medium

10.07.2012

Isolation of chromosomal DNA: E. coli strain C600 Mucts 62
Inoculation: E. coli strain DH5a and TOP10 in DYT-medium

11.07.2012

Preparation of chemically competent E. coli cells: TOP10

12.07.2012

Transformation: GFP, GFP_fusion, CFP, mRFP, RBS, P108, P100, PLac with E.coli Top10

Name	Biobrick	Plate	Well	Backbone	Resistance
GFP	[http://partsregistry.org/Part:BBa_E0040 BBa_E0040]	1	14K	pSB1A2	Ampicillin
GFP_fusion	[http://partsregistry.org/Part:BBa_K125500 BBa_K125500]	3	2P	pSB1A2	Ampicillin
CFP	[http://partsregistry.org/Part:BBa_E0020 BBa_E0020]	1	6A	pSB1A2	Ampicillin
mRFP	[http://partsregistry.org/Part:BBa_E1010 BBa_E1010]	1	18F	pSB2K3	Kanamycin
RBS	[http://partsregistry.org/Part:BBa_J61100 BBa_J61100]	1	5J	pSB1A2	Ampicillin
P108	[http://partsregistry.org/Part:BBa_J23108 BBa_J23108]	2	2E	BBa_J61002	Ampicillin
P100	[http://partsregistry.org/Part:BBa_J23100 BBa_J23100]	1	18C	BBa_J61002	Ampicillin
PLac	[http://partsregistry.org/Part:BBa_I14032 BBa_I14032]	2	11P	pSB2K3	Kanamycin

Week 2

16.07. - 22.07.2012

16.07.2012

PCR: AmiC (primer: MS1 + MS2); HU (primer: MS3 + MS4); GroES (primer: MS5 + MS6); GixR (primer: MS7 + MS8); Enhancer (primer: MS9 + MS10); ⇒ template-DNA: chromosomal DNA, annealing: 30 sec; 60 °C, elongation: 30 sec; 72 °C, 35 cycles

Inoculation: GFP; GFP_fusion; CFP; mRFP; RBS; P108; LacIQ; P100

17.07.2012

Plasmid preparation: GFP; GFP_fusion; CFP; mRFP; RBS; P108; ~~LacIQ~~; P100

18.07.2012

Agarose gel: pipet scheme

DNA Gel extraction: Enhancer; GroES; HU

GixR Hybridization

5 µl primer MS7 (100 µM) + 5 µl primer MS8 (100 µM)
- 5 min 99°C
- over night, room temperature
- -80°C

19.07.2012

Fill-in reaction (primer extension): Enhancer

Restriction: Enhancer (EcoRI/PstI)

PCR: AmiC (primer: MS1 + MS2)

⇒ template-DNA: chromosomal DNA, annealing: 30 sec; 85 °C, elongation: 36 sec; 72 °C, 35 cycles, 1) 2 µl DMSO; 1 µl chrom. DNA | 2) 2 µl DMSO; 5 µl chrom. DNA | 3) without DMSO; 1 µl chrom. DNA | 4) without DMSO; 5 µl chrom. DNA | 5) 2 µl DMSO; without chrom. DNA

Test restriction: 7) CFP (EcoRI/PstI); 8) GFP (EcoRI/PstI); 9) GFP-fusion (EcoRI/PstI); 10) mRFP (EcoRI/PstI); ⇒ all negative

Agarose gel: pipet scheme

1)|2)|3)|4)|5)|marker|7)|8)|9)|10) (bild 2)

Control digest: CFP (EcoRI/PstI); GFP (EcoRI/PstI); GFP-fusion (EcoRI/PstI); mRFP (EcoRI/PstI); ⇒ restriction over night

20.07.2012

Agarose gel: pipet scheme; ⇒ marker|GFP|GFP-fusion|CFP|mRFP (all positive)

(bild 3)

Week 3

23.07. - 29.07.2012

26.07.2012

Restriction: pSB1T3 (XbaI/SpeI and DpnI); pSB1A3 (XbaI/SpeI and DpnI); pSB1K3 (XbaI/SpeI and DpnI); pSB1C3 (XbaI/SpeI and DpnI)

Ligation: GixR + pSB1A3; Enhancer + pSB1K3; cyclisation of pSB1C3, pSB1K3, pSB1A3, pSB1T3 (couldn’t work)

Week 4

30.07. - 05.08.2012

30.07.2012

PCR: CFP (primer: MS16 + MS17) ⇒ template-DNA: BBa_E0010; ⇒ positive; mRFP (primer: MS14 + MS15) ⇒ template-DNA: BBa_E1010; ⇒ positive; Gin (primer: MS11 + MS13) ⇒ template-DNA: chromosomal DNA (that was wrong); RBS-Gin (primer: MS13 + MS12) ⇒ template-DNA: chromosomal DNA (that was wrong); ⇒ annealing: 30 sec; 60 °C, elongation: 40 sec; 72 °C, 35 cycles

Transformation: all vector-backbone-ligations; Enhancer (K3); GixR (A3)

31.07.2012

Result: transformation; pSB1A3: 3 colonies; pSB1K3: 60 colonies; pSB1C3: 9 colonies; pSB1T3: 0 colonies; Enhancer (K3): 0 colonies; GixR (A3): 0 colonies

Agarose gel: pipet scheme; ⇒ gix|marker|AmiC from 16.07.| AmiC from 16.07.| AmiC from 19.07.| AmiC from 19.07.; ⇒ all negative

(bild 4,5)

Agarose gel: pipet scheme; ⇒ marker|RBS-Gin from 30.07.|AmiC from 16.07.|Gin from 30.07.|CFP from 30.07.|mRFP from 30.07.|control; ⇒ all negative

Resuspension of a biobrick: BBa_B0010 (terminator)

DNA Gel extraction: CFP; mRFP

PCR: AmiC (primer: MS1 + MS2); RBS-Gin (primer: MS12 + MS13); Gin (primer: MS11 + MS13); ⇒ template-DNA: chromosomal DNA, annealing: 30 sec; 55 °C, elongation: 40 sec; 72 °C, 35 cycles

Restriction: pSB1A3 (EcoRI/PstI); CFP (EcoRI/PstI); mRFP (EcoRI/PstI)

Transformation: pSB1A3; pSB1C3; pSB1T3; Terminator; GixR; Enhancer

Inoculation: pSB1A3; pSB1C3; pSB1K3

Ligation: pSB1A3 + CFP; pSB1A3 + mRFP

GixR Hybridization

5 µl primer MS7 (100 µM) + 5 µl primer MS8 (100 µM)
- 5 min 99°C
- over night, room temperature
- -80°C

DNA Gel extraction: AmiC

Ligation: AmiC + pSV2 (suicide vector)

01.08.2012

Result: transformation; Only BBa_B0010 colonies present

Plasmid preparation: pSB1A3 ⇒ only clone 1, 3 Positive; pSB1C3 ⇒ all negative; pSB1K3 ⇒ all negative

Ligation: GixR hyb. + pJET2_1; ⇒ over blunt ends

Restriction: GixR hyb. (EcoRI/PstI); pSB1C3 (EcoRI/PstI)

Agarose gel: pipet scheme; Marker|RBS-Gin1 +DMSO|RBS-Gin2 -DMSO|Gin1 +DMSO|Gin2 -DMSO|control

(bild 6)

Agarose gel: pipet scheme; Marker|AmiC1 +DMSO| AmiC2 –DMSO

(bild 7)

DNA Gel extraction: RBS-Gin; Gin; AmiC

Test restriction: pSB1A3 (EcoRI)

Restriction: RBS-Gin (EcoRI/PstI); Gin (EcoRI/PstI); AmiC (EcoRI/PstI); pSB1C3 (EcoRI/PstI); pSB1K3 (EcoRI/PstI); pSB1T3 (EcoRI/PstI)

Ligation: cyclisation of pSB1T3

Fill-in reaction (primer extension): Enhancer

Ligation: Enhancer and GixR in pSV2; Enhancer in pSB1K3; GixR in pSB1C3

Agarose gel: pipet scheme; Marker| pSB1A3 1,2,3| pSB1C3 1,2,3,4| pSB1K3 1,2,3,4

(bild 8)

pSB1A3 c2

pSB1C3 c4

pSB1K3 c3

Transformation: pSB1A3 religation; CFP in A3; mRFP in A3; AmiC in pJET; GixR in pJET; Enhancer in pJET; GixR in C3; Enhancer in K3

Ligation: AmiC + pSB1T3; RBS-Gin + pSB1K3; Gin + pSB1K3

02.08.2012

Resuspension of a biobrick: pSB3C5; ⇒ for ccdB

Plasmid preparation: BBa_B0010 (terminator)

Test restriction: Terminator c1,2,3,4 (EcoRI/PstI)

Agarose gel: pipet scheme; Marker|Terminator 1,2,3,4

(bild 9)

Transformation: pSB1T3 recycled; AmiC in T3; Gin-RBS in K3; Gin in K3; pSB3C5 linear (false)

03.08.2012

Plasmid preparation: Enhancer in pJET

Week 5

06.08. - 12.08.2012

06.08.2012

Resuspension and transformation of a biobrick: BBa_J04450 in pSB1A3; BBa_J04450 in pSB1C3; BBa_J04450 in pSB1K3; BBa_J04450 in pSB1T3

Restriction: GFP-fusion (EcoRI/SpeI); Terminator (XbaI/PstI); Promoter BBa_J23100 (EcoRI/SpeI); Promoter BBa_J23108 (EcoRI/SpeI); RBS (XbaI/PstI)

Ligation: RBS-Gin in T3; Gin in T3; GFP-fusion (EcoRI/SpeI) + Terminator (XbaI/PstI) in pSB1K3; Promoter BBa_J23108 (EcoRI/SpeI) + RBS (XbaI/PstI) in pSB1K3; Promoter BBa_J23100 (EcoRI/SpeI) + RBS (XbaI/PstI) in pSB1K3

GixR Hybridization

1(3) µl primer MS7 (100 µM) + 1(3) µl primer MS8 (100 µM) + T4-Ligasebuffer
- 5 min 95°C
- over night, room temperature
- -80°C

Transformation: GixR in C3; Gin in T3; RBS-Gin in T3; mRFP in A3; CFP in A3

07.08.2012

Transformation: GFP-fusion; CFP; J23108-RBS; J23100-RBS

Plasmid preparation: GixR 1,2,3

Restriction: GixR hyb. 1,2,3 (EcoRI/PstI); pSB1C3 (EcoRI/PstI)

Ligation: GixR hyb. 1,2,3 in pJET; GixR hyb. 1,2,3 in C3

Transformation: GixR hyb. 1,2,3 in pJET; GixR hyb. 1,2,3 in C3

Test restriction: pSB3C5 (XbaI); pJET (XbaI)

Agarose gel: pipet scheme; Marker|pSB3C5 c1a,2a,3a,4a|Marker|pSB3C5 c1b,2b,3b,4b|Marker|Enhancer-pJET c1,2,3,4|Marker

(bild 10)

⇒ positive: pSB3C5 c3a,4a,3b,4b,; Enhancer-pJET c1,2,3,4

08.08.2012

Result transformation: GFP-fusion (20 clones); J23108-RBS (20 clones); J23100-RBS (20 clones); GixR hyb. 1,2,3 in pJET (10 clones); GixR hyb. 1,2,3 in C3 (10 clones); CFP (5 clones)

Restriktion: Enhancer in pJET (EcoRI/PstI); pSB1C3 (EcoRI/PstI)

Agarose gel: pipet scheme; Marker| Enhancer|pSB1C3

(bild 11)

DNA Gel extraction: Enhancer; pSB1C3

Ligation: Enhancer 1,2 in C3

Transformation: Enhancer 1,2 in C3; C3; mRFP

09.08.2012

Result transformation: GFP-fusion ⇒ positive; J23108-RBS ⇒ positive; J23100-RBS ⇒ positive; CFP ⇒ positive; GixR in C3 c1 ⇒ negative; GixR in C3 c2 ⇒ negative; GixR in C3 c3 ⇒ negative

Plasmid preparation: GFP-fusion; J23108-RBS; J23100-RBS; CFP

Test restriction: GFP-fusion (EcoRI/PstI); J23108-RBS (EcoRI); J23100-RBS (EcoRI); CFP (EcoRI/PstI)

Agarose gel: pipet scheme; Marker|GFP-fusion 1,2,3,4,5,6,7,8,9| Marker|10,11,12,13,14,15,16,17,18

(bild 12)

Marker|J23108-RBS 1,2,3,4,5,6,7,8,9| Marker|10,11,12,13,14,15,16,17,18

(bild 13)

Marker|J23100-RBS 1,2,3,4,5,6,7,8,9| Marker|10,11,12,13,14,15,16,17,18

(bild 14)

(bild 15)

Inoculation: GixR in C3; Gin in T3; Gin-RBS in T3; pSB1C3; Enhancer in C3; mRFP in A3

Week 6

13.08. - 19.08.2012

13.08.12

PCR: GroES (primer: MS5 + MS6 (b)); HU (primer: MS3 + MS4 (b)); ⇒ with and without DMSO, template-DNA: chromosomal DNA, annealing: 30 sec; 60 °C, elongation: 40 sec; 72 °C, 35 cycles

Agarose gel: pipet scheme; Marker|HU +DMSO|HU -DMSO|GroES +DMSO|GroES –DMSO|control

(bild 16)

Transformation: LacIQ (BBa_I14032)

14.08.12

Restriction: pSB1K3 (EcoRI/PstI); Enhancer 3,4 (EcoRI/ PstI); GFP-fusion (EcoRI/SpeI); Terminator (XbaI/PstI)

Test restriction: RBS-Gin in T3 (EcoRI/ PstI)

Ligation: GFP-fusion (EcoRI/SpeI) + Terminator (XbaI/PstI) in pSB1K3 (EcoRI/PstI); Promotor J23108 (EcoRI/SpeI) + RBS (XbaI/PstI) in pSB1K3 (EcoRI/PstI); Enhancer 3,4 (EcoRI/ PstI) + pSB1K3 (EcoRI/PstI)

Transformation: GFP-fusion-Terminator in pSB1K3; Promotor-RBS in pSB1K3; Enhancer 3 in pSB1K3; Enhancer 4 in pSB1K3; GixR in pJET

15.08.2012

PCR: GroES (primer: MS5 + MS6 (b)); HU (primer: MS3 + MS4 (b)); ⇒ with and without DMSO, template-DNA: chromosomal DNA, annealing: 30 sec; 55 °C, elongation: 30 sec; 72 °C or annealing/elongation: 30 sec; 72 °C, 35 cycles

Agarose gel: pipet scheme; Marker|HU +DMSO|HU -DMSO|GroES +DMSO|GroES –DMSO| HU +DMSO two-step PCR|HU -DMSO two-step PCR |GroES +DMSO two-step PCR |GroES –DMSO two-step PCR

(bild 17)

Resuspension of a biobrick: BBa_J04450 in pSB1A3; BBa_J04450 in pSB1T3; BBa_J04450 in pSB1C3; BBa_J04450 in pSB1K3

Agarose gel: pipet scheme; Marker|HU -DMSO|HU +DMSO|GroES -DMSO|GroES +DMSO

(bild 18)

⇒ 2-step PCR didn’t work, HU 1,2

DNA Gel extraction: HU 1,2

Transformation: BBa_J04450 in pSB1A3; BBa_J04450 in pSB1T3; BBa_J04450 in pSB1C3; BBa_J04450 in pSB1K3

Test restriction: pSB1T3 (EcoRI/PstI and DpnI); pSB1K3 (EcoRI/PstI and DpnI); pSB1C3 (EcoRI/PstI and DpnI); pSB1A3 (EcoRI/PstI and DpnI)

16.08.2012

PCR: GroES (primer: MS5 + MS6 (b)); ⇒ with and without DMSO, template-DNA: chromosomal DNA, annealing: 30 sec; 55 °C, elongation: 30 sec; 72 °C , 35 cycles

Agarose gel: pipet scheme; Marker| GroES 1, 2 +DMSO

(bild 19)

Plasmid preparation: P-RBS

Test restriction: P-RBS (EcoRI/PstI)

Agarose gel: pipet scheme; control|P-RBS|marker

(bild 20)

Restriction: Enhancer 3,4 (EcoRI/ PstI); HU (EcoRI/ PstI); AmiC (EcoRI/ PstI); Promoter, GFP (EcoRI/SpeI); RBS; Terminator (XbaI/PstI)

Ligation: HU, AmiC in pSB1A3; Enhancer 3,4 in pSB1K3; P-RBS in pSB1K3; GFP fusion-Terminator in pSB1K3

DNA Gel extraction: GroES 1, P-RBS

Transformation: AmiC; HU; Enhancer 3,4, 3 alt,4 alt

Inoculation: BBa_J04450 in pSB1A3; BBa_J04450 in pSB1T3; BBa_J04450 in pSB1C3; BBa_J04450 in pSB1K3; AmiC; P-RBS

17.08.2012

Restriction: GroES (EcoRI/SpeI)

Ligation: GroES in pSB1C3

Transformation: GroES in pSB1C3

Test restriction: P-RBS (EcoRI/PstI); BBa_J04450 in pSB1A3 (EcoRI/PstI); BBa_J04450 in pSB1T3 (EcoRI/PstI); BBa_J04450 in pSB1C3 (EcoRI/PstI); BBa_J04450 in pSB1K3 (EcoRI/PstI)

Agarose gel: pipet scheme; marker|BBa_J04450 in pSB1A3 1,2,3,4|BBa_J04450 in pSB1K3 1,2,3,4| marker| BBa_J04450 in pSB1C3 1,2,3,4

(bild 21)

Agarose gel: pipet scheme; marker|P-RBS 1,2,3,4| P-RBS 1,2,3,4| marker| BBa_J04450 in pSB1K3 1,2,3,4

(bild 22)

Week 7

20.08. - 26.08.2012

20.08.2012

PCR: Backbone (primer MS24 + MS25); ⇒ template-DNA: pSB1A3, pSB1T3, pSB1C3 and pSB1K3, annealing: 30 sec; 55 °C, elongation: 30 sec; 72 °C , 35 cycles

Agarose gel: pipet scheme; marker|: pSB1A3|pSB1T3|pSB1C3|pSB1K3

(bild 23)

Transformation: BBa_JH023

Inoculation: GroES; P-RBS; GFP-T; Enhancer 3,4; AmiC; P-RBS alt; GFP-T alt

21.08.2012

Results: colonies of BBa_JH023; inoculations except AmiC and P-RBS alt successful

PCR: pSB1A3-BBa_J04450 (template DNA); pSB1T3-BBa_J04450 (template DNA); pSB1C3-BBa_J04450 (template DNA); pSB1K3-BBa_J04450 (template DNA); used primer --> MS24Prefix_rev + MS25Suffix_fwd; initial denaturation 98°C - 5min; denaturation: 98°C - 1min; annealing: 55°C - 30s; elongation: 72°C - 2.5min -->repeat 35 times; 72°C - 5min --> 4°C - ∞

miniprep: GroES, Enh 3/4 (+old), P-RBS (+old), GFP-T (+old)

Test restriction: of miniprep; over night, 37°C

Agarose gel (1%): watch pic

Inoculation: E.coli BBa_I14032; over night, 37°C

22.08.2012

PCR: CFP; mRFP; initial denaturation 98°C - 5min; denaturation: 98°C - 10s; annealing: 60°C - 30s; elongation: 72°C - 40s -->repeat 35 times; 72°C - 5min --> 4°C - ∞

Agarose gel (1%): watch picture

miniprep: of LacIQ

Test restriction: of LacIQ with EcoRI and PstI; watch picture

Agarose gel: test restriction of GroES and GFP-T (->21.08.12), gel 1%; watch picture; test restriction of Enhancer (->21.08.12), gel 2%; watch picture; test restriction of Enhancer and P-RBS (->21.08.12), gel 2%; watch picture

23.08.2012

Svetti please check! -->lacIQ evtl ganz rausnehmen?! ;)

24.08.2012

Svetti please check!

Week 8

27.08. - 02.09.2012

27.08.2012

Results: CFP: 1 colony; CFP (neu): Colonies; mRFP: colonies; mRFP (neu): no colonies

PCR: template: backbones (pSB1K3/T3/C3/A3; parameters: 98°C 5min, >> 98°C 1min, 70°C 30s, 72°C 2.5min << x30, 72°C 5min, 4°C ∞

colony-PCR: parameters: 98°C 5min, >> 98°C 1min, 72°C 1min << x30, 72°C 5min, 4°C ∞

Agarose gel of backbone PCR: no result

elution of the backbones of Friday the 24th

Agarose gel of colony PCR: watch picture

Inoculation: pSB1C3_...; mRFP clone 20,24; CFP clone 14,15,17,18; gix clone 1,2; 5ml LB, over night, 37°C

28.08.2012

production of competent TOP10

PCR: Enhancer, Terminator, Gix, P-RBS; parameters: 98°C 5', 98°C 1', 66°C 30", 72°C 30", 72°C 5', 4°C ~; watch picture

Transformation: pBad, araC, pSacB; over night, 37°C

miniprep: GixR (1,2); CFP (14,15,17,18); mRFP (20,24); alle in pSB1C3

29.08.2012

Results: Transformation: no colonies

PCR: Terminator, Gix, Enhancer, P-RBS; diluted templates: Terminator, P-RBS, Gix 1 --> 1:10; Enhancer, Gix 2 --> 1:20; watch picture

3AA: CFP, mRFP with Terminator; 2µl DNA; 1µl SpeI; 2µl Tango; 15µl dH2O; --> 1h at 37°C; +1µl EcoRI; +2,5µl Tange; --> 1h at 37°C; --> inactivation for 20min at 80°C

Ligation: 3AA products in pSB1T3; 18.5µl H2O; 2.5 µl Buffer; 1µl Insert CFP or mRFP (EcoRI + SpeI); 1µl Insert Terminator (BBa_B0010) (XbaI + PstI); 1µl pSB1T3 (EcoRI + PstI); 1µl Ligase; --> 1h at RT

Transformation: pBad --> TOP10 + pSB2K3; CFP-T, mRFP-T --> TOP10 + pSB1T3

Sequencing: bitte mal nachschlagen, die Notizen peil ich nicht ;)

30.08.2012

Results: Transformation: no colonies --> testing Trafo with BBa_J04450 A/K/T/C; 2 colonies at pBad-Trafo from 28.08.2012 --> liquid culture for miniprep; 1 colony at pSacB-Trafo from 28.08.2012 --> tested on succrose-sensitivity

31.08.2012

PCR: SacB; Parameters No.1: 95°C 5', >>95°C 30", 60°C 30", 72°C 1'<< x30, 72°C 5', 4°C; Parameters No.2: 95°C 5', >>95°C 30", 72°C 1.5'<< x30, 72°C 5', 4°C

Agarose gel: watch picture; cut out lines at 1.5kb

Ligation: 3AA (CFP-T, mRFP-T); watch 29.08.; used vector: pSB1K3/T3

Transformation: of ligation in TOP10

miniprep: pBad/araC K.1+2

restriction: GixR rehybridization; cut with EcoRI and PstI

ligation: 1µl GixRhyb E+P; 1µl pSB1C3 E+P; 1µl Th-Pol; 2µl Buffer; 15µl dH2O

Transformation: ligation + TOP10 --> LB(cam)

Results of test-trafo: Amp, Km, Cm OK --> Km with fewer colonies; Tet --> hardly colonies; --> comp.TOP10 obviously all right, exclusion of Tet in future work

Week 9

03.09. - 09.09.2012

03.09.2012

Results: Transformation; GixR in C3 --> no colonies; CFP-T/mRFP-T in C3(31.8.) --> no colonies; CFP-T/mRFP-T in T3(31.8.) --> many but small colonies; CFP-T/mRFP-T in T3(29.8.) --> less colonies

PCR: of colonies (CFP-T, mRFP-T); parameters: 98°C 5', >>98°C 1', 72°C 1'<<x30, 72°C 5', 4°C

Agarose gel: 6x colony pT3-CFP-T from 29./31.8.; 6x colony pT3-mRFP-T from 29./31.8.; pC3-CFP (14); pC3.mRFP (24); result watch picture

Week 10

10.09. - 16.09.2012

11.09.2012

microscopy-screening: GroES-GFP ⇒; no fluorescence; GroES-CFP ⇒; no fluorescence; AmiC-mRFP ⇒; no fluorescence; AmiC-GFP ⇒; no fluorescence

colony-PCR: GixR; RBS-Gin; Terminator

3A-Assembly (digestion, ligation, transformation): GroES (E/S) + Terminator (X/P) + pSB1K3 (P/E); AmiC (E/S) + Terminator (X/P) + pSB1K3 (P/E)

plasmid-prep and control-digestion (E/P): GroES-GFP; GroES-CFP; AmiC-mRFP; AmiC-GFP; GroES-Terminator; Enhancer; GFP-Terminator; Terminator

@@ Line 132: / Line 132: @@
 ==16.07.2012==
 ; PCR
-: AmiC (primer: MS1 + MS2)
+: AmiC (primer: [[Team:Marburg_SYNMIKRO/Primer#MS1|MS1]] + [[Team:Marburg_SYNMIKRO/Primer#MS2|MS2]])
 : HU (primer: MS3 + MS4)
 : GroES (primer: MS5 + MS6)

Team:Marburg SYNMIKRO/Notebook