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DateSummary
Anchor
6
6
06/01
  •  h:Lyn-TEV Colonies Picked
  • h:CDB-RFP-G4 transformation
  • h:CDA-RFP-G4 Sequence Analysis
  • Inocculate Midipreps
  • h:Lyn, h:CDB-TCS-G4 cryostocks
06/02
  • Cloning Redesign
  • Pick hEF1a:CD79B-pTet:RFP-Gal4VP16 Colonies
06/03
  • Miniprep hEF1a:CD79B-pTet:RFP-Gal4VP16
  • Cryostock hEF1a:CD79A-pTet:RFP-Gal4VP16
06/04
  • Glycerol Stock hEF1a:CD79A-pTet:RFP-Gal4VP16
  • Midiprep 4 Frozen pellets
  • Digest & Gel hEF1a:CD79B-pTet:RFP-Gal4VP16
06/08
  • hEF1a:CD79B-pTet:RFP-Gal4VP16 Digest & gel
06/09
  • Send for sequencing
06/11
  • Sequencing Analysis
  • Glycerol Stock H:CDA-RFP-G4
06/16
  • designed SDM primers
  • LR TRE:mKate, hEF1a:LacI, pLac:mKate
  • experimental design + deadlines
06/17
  • annealed linker halves
  • CD79A linker golden gates
06/18
  • transformed CD79A linker golden gates
  • transformed LRs (TRE:mKate, pLac:mKate, hEF1a:LacI)
  • LRed TREt:VP16Gal4
06/19
  • sdm primers are here
  • killed LR TREt:VP16Gal4
  • Transformed LR TREt:VP16Gal4
  • Re-transformed CA-9T6-G4
  • picked CD79A linker colonies
06/21
  • picked CA-9T6-G4 colonies
06/22
  • mini CD79A linkers
  • mini TRE:mKate, pLac:mKate, hEF1a:LacI
  • digest
  • run CD79B SDM gel
06/23
  • digests and gels for TRE:mKate, pLac:mKate, hEF1a:LacI
  • kill TRE:Gal4VP16 LR
  • transform TRE:Gal4VP16 LR
  • run SDM on gel -> gel extraction
  • CD79B-RFP-G4 SDM product transformation
06/24
  • SDM CD79B-RFP-Gal4
  • SDM DpnI digest
  • transform SDM product
  • transform TRE:Gal4VP16
06/25
  • redigest TRE:mKate, pLac:mKate, hEF1a:LacI
  • PCR syk, tevp, ttevp
  • gel verify PCRs and digested LRs
  • TRE:gal4VP16 pick colonies and minipreps
  • PCR purification of syk, tevp, ttevp
  • reLR of TRE:mKate, pLac:mKate, hEF1a:LacI
  • retransform SDM digests
06/26 
06/29 

Make a whole buncha plates

label gel station so people stop making gels.

 

 

 

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