Team:Technion/13 September 2012

From 2012.igem.org

Revision as of 09:02, 20 September 2012 by Hila K R (Talk | contribs)



Team:Technion/13_September_2012
March
MTWTFSS
      1 2 3 4
5 6 7 8 9 10 11
12 13 14 15 16 17 18
19 20 21 22 23 24 25
26 27 28 29 30 31
April
MTWTFSS
            1
2 3 4 5 6 7 8
9 10 11 12 13 14 15
16 17 18 19 20 21 22
23 24 25 26 27 28 29
30
May
MTWTFSS
  1 2 3 4 5 6
7 8 9 10 11 12 13
14 15 16 17 18 19 20
21 22 23 24 25 26 27
28 29 30 31
June
MTWTFSS
        1 2 3
4 5 6 7 8 9 10
11 12 13 14 15 16 17
18 19 20 21 22 23 24
25 26 27 28 29 30
July
MTWTFSS
            1
2 3 4 5 6 7 8
9 10 11 12 13 14 15
16 17 18 19 20 21 22
23 24 25 26 27 28 29
30 31
August
MTWTFSS
    1 2 3 4 5
6 7 8 9 10 11 12
13 14 15 16 17 18 19
20 21 22 23 24 25 26
27 28 29 30 31
September
MTWTFSS
          1 2
3 4 5 6 7 8 9
10 11 12 13 14 15 16
17 18 19 20 21 22 23
24 25 26 27 28 29 30
October
MTWTFSS
1 2 3 4 5 6 7
8 9 10 11 12 13 14
15 16 17 18 19 20 21
22 23 24 25 26 27 28
29 30 31
November
MTWTFSS
      1 2 3 4
5 6 7 8 9 10 11
12 13 14 15 16 17 18
19 20 21 22 23 24 25
26 27 28 29 30


Ilya

- Began working on adding our parts to the registry.

Inbal

- Restriction for BBa_B0015 (ter+pSB1AK3) with XbaI (3189bp).
- 2 starters of T3 RNAP with CM resistance (BBa_K346000).

Asaf

I figured that I don't have enough insert (Riboswitch with polymerase) for ligation with the Psb1c3.
I have decided to extract more insert from gel from the product I got from the fusion PCR with Tm of 55C.
I couldn't find the T7* product. I have already used both products of T7.
So I ran the Riboswitch with the K1F, T3 and N4 polymerase genes on an extraction gel.
I got the expected bands,but I didn't get the 1Kb pattern, and cut the 3.2 kb bands (as I expected from previuos gels).

I cleaned the DNA from the gel.
I cut all of my inserts (Riboswitch with different polymerases) with EcoRI and PstI.
I also helped Evgeni and made glycerol stocks of his starters,
and also centerfuge the starters so that he could miniprep them tomorrow.

Hila

- Last and final colony PCR for fragments 1C, 4C, 6C and 7C in the pSB1C3_MCS plasmid. No positive colonies were found.
- In addition I made a PCR reaction for fragments 1C, 4C, 6C, 7C just in case I won't find positive colonies. The PCR for fragments 1C and 6C didn't work again…
- Additional amplification to F4, F4* and F5. In addition today the 250bp overlap primer arrived, so I amplified fragment F4' which will help us in the Gibson assembly calibration.

Lior

Noa

Evgeni

Shahar

Rachel