Team:Evry-Genopole/Notebook/June/22
From 2012.igem.org
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<FONT SIZE=3>'''Bacterial Transformation'''</FONT> <br/> | <FONT SIZE=3>'''Bacterial Transformation'''</FONT> <br/> | ||
- | 'Bacteria': T10<br/> | + | '''Bacteria''': T10<br/> |
- | 'DNA': pCS2 (+) at 640 ng.uL-1<br/> | + | '''DNA''': pCS2 (+) at 640 ng.uL-1<br/> |
1) Keep constantly the cells on ice <br/> | 1) Keep constantly the cells on ice <br/> |
Revision as of 15:39, 29 June 2012
Promoters & Reporters workgroup
Bacterial Transformation
Bacteria: T10
DNA: pCS2 (+) at 640 ng.uL-1
1) Keep constantly the cells on ice
2) Add 1 uL of pCS2 (+) in 100 uL of T10
3) Incubate 30 min on ice
4) Heat shock the cells during 30 sec at 42 degree Celsius in a water-bath without shaking
5) Put 2 min on ice
6) Add 500 uL of pre warmed SOC-medium
7) Incubate 1h at 37 degree Celsius at 225 rpm
8) Spin at 5000 rpm during 30 sec
9) Remove 150 uL - 400 uL of supernatant
10) Resuspend the pellet in the 150 uL left
11) Spread on appropriate plates
12) Incubate overnight at 37 degree Celsius
List of promoters received:
p2 Flk-1
p2 Xlurp
p2 foxi short
p2 foxi long
p2 pax3
p2 Ef1a
p2 Rosa26
p2 LMO2 short
p2 LMO2 long
p2 vast
p2 HB9
p2 NBT
p2 HSP70
p2 pax6
p2 CMV
p2 brachyury
p2 vimentin
p2 14 xUAS E1b-ATG