Team:USC/Notebook/Week1

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<h1 style="font-family:Verdana;font-weight:700;">Brainstorming</h1>
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[[Team:USC/Notebook/Week13|Week 13-14]]
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[[Team:USC/Notebook/Week14|Week 14]]
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<h3 style="font-family:Verdana; font-weight:700;background-color: #F0F0F0;">'''Week 1:'''</h3>
<h3 style="font-family:Verdana; font-weight:700;background-color: #F0F0F0;">'''Week 1:'''</h3>

Revision as of 03:19, 29 September 2011

USC Banner.jpg


Brainstorming

Brainstorming
Brain storm.JPG

Week 1
Week1.jpg

Week 2
Week2.jpg

Week 3
Week3.jpg

Week 4
Week4.jpg

Week 5
Week5.jpg

Week 6
Week6.jpg

Week 7
Week7.jpg

Week 8
Week8.jpg

Week 9
Week9.jpg

Week 10
Week10.jpg

Week 11
Week11.jpg

Week 12
Week12.jpg

Week 13
Week13.jpg

Week 14
Week14.jpg

Week 1:

06/07/2011
Transformation plasmids into DH5α Competent cells
Plasmids are from iGEM plates:
A. Plate 2 Well 7E (AHL signaling)
B. Plate 3 Well 20F (LovTAP composite)
C. Plate 4 Well 16O (LovTAP Composite)
D. Plate 1 Well 2B (GFP+PEST191)
E. Plate 2 Well 4A (Yeast ADH1 promoter)


06/08/2011
Transformation of E. Coli, Plasmids are from iGEM plates:
Plasmids are from iGEM plates:
A. Plate 2 Well 13J
B. Plate 1 Well 20F
C. Plate 4 Well 16M
D. Plate 1 Well 16K
E. Plate 3 Well 14H
F. Plate 4 Well 6O

06/09/2011
1. Inoculation for all the plasmid we have transformed before. Observation: all transformation except BBa-I15010

06/10/2011
1. Freeze the inoculated culture
2. Observation: BBa-I15008 and BBa-I63009don’t have as much growth as others

06/11/2011
1. Purify plasmid DNA from the culture
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