Team:University of Lethbridge/Notebook/Project1July

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July 1, 2008

Nathan Puhl

Subcultured RP1616 into liquid LB and pTopp cells into liquid LB + amp

July 2, 2008

Nathan Puhl, Christa, Munima

Plasma mini prepped pTopp cells

Attempted to make RP1616 cells competent using the open wet ware protocol. 100 uL aliquots of cells were froxen in liquid nitrogen and stored in the -80 freezer.

Ran CheZ in pUC19 plasmid and pUC19 plasmid from last year with high range ladder. The pUC19 plasmid seems weird, I don't think it should have two bands; I will have to ask someone about that. The CheZ plasmid appears to be the right size (2600 + 620 = 3220 bp)

Puc19 + cheZ.jpg

July 3, 2008

Nathan Puhl, Munima, Christa

No colonies on either plate, but the max-efficiency DH5-alpha cells transformed with pSB1A7 were successfully transformed (~1500 cfu). There are two possibilities: 1. the cells are competent but are low efficiency and we did not add enough DNA, or 2. The cells are not competent. To assess possibility one we will try more DNA. If that does not work we will try a protocol using electroporation.