From 2008.igem.org
(Difference between revisions)
|
|
Line 21: |
Line 21: |
| | | |
| | | |
- | <h3>Preparation of alpha_A construct</h3> | + | <h3>Preparation of alpha_A construct (second attempt)</h3> |
| <h4>Antoni</h4> | | <h4>Antoni</h4> |
| <p> | | <p> |
Revision as of 03:40, 29 October 2008
|
|
|
|
MutD5 testing
Emilia
-
Inoculation MutD5 from previous day to new medium (liquid LB + 0.25mM IPTG + kanamycin + tetracyclin + 50 μl/ml + prey)
- 6 hours culture
-
Inoculation MutD5 from the morning to new medium (liquid LB + 0.25mM IPTG + kanamycin + tetracyclin + 50 μl/ml + prey)
Mutagenesis of protein APaweł
- Results of mutagenesis: no colonies on any plate.
- Mutagenesis repeated with modified conditions: fresh stock of dNTPs used and additional MgCl2 added.
Preparation of alpha_A construct (second attempt)
Antoni
- PCR on pKS plasmid containing protein A with
AL+link10+homo2 and AP+NotI
primers and 10% DMSO(20 cycles, elongation 40 s, annealing temperature 72°C).
- PCR on pUC19 plasmid with
AlphaL+SacI and AlphaP+link10+homo2
primers (20 cycles, elongation 45 s, annealing temperature 63°C).
As a result we got two PCR products (alpha-linker and linker-A) wich will be utilized as templates in next PCR.
- Gel electrophoresis of PCR products and gel-out of proper bands (alpha_linker - 570 bp and linker_A - 470 bp ).
- Measurment of concentration of both isolated products.
Piotr
- E. coli TOP10 transformation with overnight ligation of pSB1A3 and ΔA DNA fragments.
- Plating on LB + ampicillin.
|
|