From 2008.igem.org
Notebook
To Do List
-redo PCR of CrtI with giant primers to eliminate PstI sites and cut the PCR product with PstI to select only for "fixed" fragments (Dave and Lisa)
-cut and ligate the synthetic operon now that we have the genes cloned (Lisa, Ed, Brendan)
-test GFP tagged Klebsiella (Tin) and E. coli nissler (Brendan) in vivo to ensure plasmids work and those microbes are competitive
-attempt another lactobacilli electroporation (Brendan and Tin)
-cut and ligate RNAi constructs together (Moffman and Jen)
-work out deal to print T-shirts (Moffman)
-write more grants to Special grants and CSA - other fundraising ideas welcome (Jen)
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