Team:BCCS-Bristol/Calendar-Notebook/1 July 2008

From 2008.igem.org

(Difference between revisions)
Line 1: Line 1:
 +
<html><link rel="stylesheet" href="http://www.chofski.co.uk/iGEM/bccs-igem.css" type="text/css"></html>
 +
__NOTOC__
 +
<div class="bccsNavBar">
 +
{|  align="center"
 +
!align="center"|[[Team:BCCS-Bristol|Home]]
 +
!align="center"|[[Team:BCCS-Bristol/Team|The Team]]
 +
!align="center"|[[Team:BCCS-Bristol/Project|The Project]]
 +
!align="center"|[[Team:BCCS-Bristol/Parts|Submitted Parts]]
 +
!align="center"|[[Team:BCCS-Bristol/Modeling|Modelling]]
 +
!align="center"|[[Team:BCCS-Bristol/Notebook|Wet Lab]]
 +
!align="center"|[[Team:BCCS-Bristol/Calendar|Calendar]]
 +
!align="center"|[[Team:BCCS-Bristol/Misc|Miscellaneous]]
 +
|}
 +
<br>
 +
</div>
 +
This is a page for any solutions
This is a page for any solutions

Revision as of 13:55, 24 July 2008

This is a page for any solutions

Media for Plates 0.3% 400ml 0.15% 150ml 0.5% 150ml
Bactotryptone4g1.5g1.5g
NaCl2g0.75g0.75g
BactoAgar1.2g0.225g0.75g

in addition did a streak out for master colonies of MG1655 in LB from table below overnight at 37oC

10ml LB '
Yeast Extract0.05
Tryptone0.1
Nacl0.1



SOC medium in preparation for Biobrick transformation this consisted of

Trypton 2g
Yeast Extract0.5g
NaCl0.05g

in 95ml of water, then autoclaved. after this add this:

MgCl2 0.5ml 2M solution
Glucose2ml 1M

then freeze at -20oC. this solution is from Molecular Cloning 3 A.2 SOB/SOC Medium.