IGEM:MIT/2006/Notebook/2006-8-1
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to do (am)
- ask Isadora to help with fax machine
- order new pchA reverse primer (ask Tom for help?)
- run a gel of BAT2 and THI3 pcr products
- test osmY+E0840(A,B,C) part with plate reader
- miniprep/nanodrop 7 overnight liquid cultures
- repeat failed/funky digestions (and run gel --NO GEL EXTRACTION)
to do (pm)
- nanodrop and run a gel of digest products (NO GEL EXTRACTION)
- do ligations using new 8/1 digest products
- transform
repeat failed/funky digestions (and then gel extract)
- R0040: SP
- RBS30A-ATF1mut: ES
- RBS30B-ATF1mut: ES
- RBS30C-ATF1mut: ES
- RBS32A-ATF1mut: ES
- RBS32B-ATF1mut: ES
- RBS32C-ATF1mut: ES
other cut pieces we have ready to use
- B0015: EX
- B0030: SP
- B0032: SP
- R0040:SP (didn't show with 5μL loaded on wide lane gel, but could still be there)
ligations (with 7/31 gel extract pieces 1-8 above)
- R0040+1->Prom-RBS30A-CDS-Term
- R0040+2->Prom-RBS30B-CDS-Term
- R0040+3->Prom-RBS30C-CDS-Term
- 4+Term->RBS32C-ATF1mut-Term
- 5+Term->RBS32A-ATF1mut-Term
- 6+Term->RBS30A-ATF1mut-Term
- 7+Term->RBS30B-ATF1mut-Term
- R0040+8(E0840)->CP-RBS-GFP-Term
transformations (@ 2:30 pm)
- prepare 9 plates, review the resistance of backbones
- use fresh Top10 cells, pUC19 control, 200 μL