Team:ESBS-Strasbourg/15 July 2008

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DryLab

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General Layout and content (MM)

Modeling

  • heavy work on the model (RS)

WetLab

Paul: -PCR of Gal4 and VP16 from the plasmid given by marielle
conditions: 100ng plasmid, 2.5µL primers, pFusion+MgSO4 buffer 5µL, 5µL dNTP (2mM), pFusion 1u
=>No amplifications, no trace of primers after gel migration (1g agar in 100mL, 100V)

-second migration:
same PCR gal4 product (20 µL in gel this time)
same PCR vp16 product (20 µL in gel this time)
Vp16 for: 1.25µL in 25µL
Vp16 rev: 1.25µL in 25µL
Gal4 for: 1.25µL in 25µL
Gal4 for: 2.5µL in 25µL
Gal4 for: 3.75µL in 25µL

General

Quote of the day

"I think that our WetLab-Team goes swimming..." (MW)

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