Team:TUDelft/30 July 2009

From 2009.igem.org

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(Tim Weenink)
(Tim Weenink)
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Ligated and transformed assemblies according to protocol.
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15:20 Plated assemblies
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15:20 Done plating the assemblies.
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15:40 inoculated *S and *T cultures, four colonies each
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15:40 inoculated (2*4) *S and *T cultures
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16:55 Inoculated !A cultures from glycerole stock. Two tubes.
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16:55 Inoculated 2 !A cultures
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===Calin===
===Calin===

Revision as of 19:24, 30 July 2009

Lab Notebook

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30 July 2009

Tim Weenink

prepared assembly mixes for !B, !C and !D constructs. Standard Ginko assembly kit was used. DNA concentrations as below (these mixtures were added to 7.5 µl of digestion mixture):

Assembly name position Components volume in µl
 !B Upstream  !A DNA 33.0
H20 9.5
Downstream BBa_B0015 DNA 10.0
H20 32.5
Backbone pSB1AC3 DNA 6.5
H20 36
 !C Upstream BBa_R0040 DNA 10.0
H20 32.5
Downstream *I6 DNA 5.5
H20 37.0
Backbone pSB1AC3 DNA 6.5
H20 36
 !D Upstream *I6 DNA 5.5
H20 37.0
Downstream BBa_K145201 DNA 18.0
H20 24.5
Backbone pSB1AC3 DNA 6.5
H20 36

Ligated and transformed assemblies according to protocol.

15:20 Done plating the assemblies.

15:40 inoculated *S and *T cultures, four colonies each

16:55 Inoculated !A cultures from glycerole stock. Two tubes.

Calin

Plated three backbones left over from the transformation the other day. Did a digest on oriT-R with E and P.


Tim Vos

Minipreped pSB4C5, pSB.