Difference between revisions of "20.109(F17): Notes for M1"

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(M1D2)
(M1D1)
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*100ml glass bottles near weigh station
 
*100ml glass bottles near weigh station
 
*pre-cut gel bond at front bench
 
*pre-cut gel bond at front bench
 +
*Secure line II pen
  
 
===M1D2===
 
===M1D2===

Revision as of 17:45, 11 September 2017

20.109(F17): Laboratory Fundamentals of Biological Engineering

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       1. Measuring Genomic Instability        2. Manipulating Metabolism        3. Engineering Biomaterials              

M1D1

Per group, aliquot in Tissue Culture, sterile

  • 14ml of DMEM media
  • 3ml of PBS
  • 1ml of trypsin
  • set aside T75 flask

Per group

  • 50 mL 1x PBS in bottle
  • cylinder near weight station for PBS
  • 100ml glass bottles near weigh station
  • pre-cut gel bond at front bench
  • Secure line II pen

M1D2

Per group, aliquot

  • in main lab
    • 1x PBS glass bottle
    • 2 eppendorf tubes of LMP agarose (in eppendorf water bath)
    • print a large scheme of the plate so they can keep track of how to load chips
  • and separately, in the TC hood,
    • 5 mL 1x PBS
    • 10 mL MEF media
  • 4 binder clips
  • 1 glass slide
  • 1 bottomless 96-well plate
  • 1 razor blade
  • Pasteur pipets
  • sharp jar
  • pipet aid
  • team sticker to identify glass slides
  • printout of today's protocol
  • large scheme of the plate to hang in TC so they can keep track of how to load chips