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To Do

  •      Monday morning
  •      Monday afternoon
  •          pick colonies from gibsons
  •          retransform Lyn, all the TRE parts.
  •          Pick colonies from APP, APPSwe
    Gibsons shouldn't exceed 30C, they are big and will recombine strangely at 37

Monday

  •  Tissue Culture
    •  Seed 3 plates (2 w/ glass cover slips 1 standard)
    •  Dilute remaining DNA
    •  Update Experiments Pages
    •  Experiment Timeline
  •  Cloning
    •  Transform
      •  TRE: Lyn-mKate verified mini
      •  TRE: Lyn-TEV LR
      •  TRE: Gmab L verified mini
      •  TRE: CD79B verified mini
      •  TRE: CD79A verified mini
      •  hEF1a: Lyn LR
      •  TRE: Syk-eYFP LR
    •  Pick Colonies
      •  A/B
      •  A4/B
      •  A/B4
      •  A4/B4
    •  LR
      •  TRE: Gmab H

 

Friday

  •  TC
    •  Dilute Midipreps
    •  Update Experiments Pages
    •  Experiment Timeline
    •  Seed
  •  Cloning
    •  Plasmids Library
  •  Thursday----------------------------------------------------------------------------------------
  •  TC
    •  Dilute Midipreps
    •  Stain Slides
    •  Finish Planning
    •  add Dox
    •  Seed?
  •  Wednesday-------------------------------------------------------------------------------------
  •  TC
    •  Path Foreward
    •  Dilute Midipreps
    •  Transfect
      •  Tango 2
      •  Membrane Localization Dilution Microscopy

Future

Process gibsons and APP stuff: minis, verify, grow midi, midi

grow minis, run minis, verify, grow midi, midi

pEXPR 6?

Plasmids library

digest app stuff

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