IGEM:MIT/2006/Notebook/2006-8-30: Difference between revisions

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#glycerol new Q119 '''-done'''
#glycerol new Q119 '''-done'''
#sequence osmY (SO and SN) constructs in bright green box b/c smell test data is not on wiki '''-done'''
#sequence osmY (SO and SN) constructs in bright green box b/c smell test data is not on wiki '''-done'''
#resequence 0-Q-199A in case rerun doesn't work '''-done'''
#3-part assemble rbss to pchBA.15-muts and transform into top10 '''-done'''
#3-part assemble rbss to pchBA.15-muts and transform into top10 '''-done'''
#consider transforming O-Q-119 and O-Q-199 (?) into IK to smell test '''-done'''
#consider transforming O-Q-119 and O-Q-199 (?) into IK to smell test '''-done'''

Revision as of 12:01, 30 August 2006

to do

  1. digest J45298 miniprep (from 8/29) with XP (run a gel to make sure it looks correctly mutagenized) -done
  2. glycerol-done/miniprep -done/sequence J45396 -done
  3. glycerol new Q119 -done
  4. sequence osmY (SO and SN) constructs in bright green box b/c smell test data is not on wiki -done
  5. resequence 0-Q-199A in case rerun doesn't work -done
  6. 3-part assemble rbss to pchBA.15-muts and transform into top10 -done
  7. consider transforming O-Q-119 and O-Q-199 (?) into IK to smell test -done
  8. pick multiple colonies from 30.BAT.30.THI3.15 (i.e. J45399) plates and make LCs -done
  9. LC whatever we need for an osmY-Q0440-E0840 plate reader test (and sign up for the block)
  10. smell the pseudomonas cultures (with added methyl salicylate) to see if their minty-ness degraded overnight -done

do tomorrow

  1. primers should be arriving today, so we should try to PCR pmsCEAB-full out of PE3 and pE3R (minipreps of both plasmids from 8/29)
  2. check if the 0-Q-199A forward sequencing is in from the re-run and see if it looks good

help

  1. UPDATE REGISTRY: create registry biobrick parts and choose numbers for our inverter constructs (w/ and w/out osmY attached) as well as put all intermediate BGD, IAGD, SAGD parts into the registry!!!! - p.s. anybody out of town is welcome to help. we seem to be very behind on this.