IGEM:MIT/2006/Notebook/2006-9-11: Difference between revisions

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==to do==
==to do==
#analyze 24 sample sequence order
#analyze 24 sample sequence order (contains 399s and 320s) '''-done: KB, but would love for somebody else to check also'''
#*pending these sequences: we should (if neccesary) miniprep/sequence duplicates to try again
#*glycerol/miniprep/sequence any possibly correct 400 LCs in fridge
#do antartic phosphotase step to y0078:xs and y0080:xs digests from 9/9 '''-done, SP'''
#ligate y0078 and 70080 to J45014:XS (already cut and ready to go in corner of orange digest tray) '''-done, SP'''
#transform yeast vector constructs in regular top10 e.coli '''-done, SP and VV'''
#start LCs for testing osmY-inverter in the plate reader '''-done, KB: put 7 tubes into 37 room'''

Latest revision as of 15:42, 11 September 2006

to do

  1. analyze 24 sample sequence order (contains 399s and 320s) -done: KB, but would love for somebody else to check also
    • pending these sequences: we should (if neccesary) miniprep/sequence duplicates to try again
    • glycerol/miniprep/sequence any possibly correct 400 LCs in fridge
  2. do antartic phosphotase step to y0078:xs and y0080:xs digests from 9/9 -done, SP
  3. ligate y0078 and 70080 to J45014:XS (already cut and ready to go in corner of orange digest tray) -done, SP
  4. transform yeast vector constructs in regular top10 e.coli -done, SP and VV
  5. start LCs for testing osmY-inverter in the plate reader -done, KB: put 7 tubes into 37 room