Team:Technion/13 September 2012
From 2012.igem.org
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I also helped Evgeni and made glycerol stocks of his starters,<br> and also centerfuge the starters so that he could miniprep them tomorrow. | I also helped Evgeni and made glycerol stocks of his starters,<br> and also centerfuge the starters so that he could miniprep them tomorrow. | ||
==Hila== | ==Hila== | ||
+ | - Last and final colony PCR for fragments 1C, 4C, 6C and 7C in the pSB1C3_MCS plasmid. No positive colonies were found. <br> | ||
+ | - 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… <br> | ||
+ | - 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. <br> | ||
==Lior== | ==Lior== |
Revision as of 09:02, 20 September 2012
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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.