User:Karmella Haynes/Notebook/PcTF Genomics/2014/09/23: Difference between revisions

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'''Transductions'''<br>
'''Transductions'''<br>
Note: cells are in standard complete medium
# Plate 1: U2OS
# Plate 1: U2OS
# Plate 2: SK-N-SH
# Plate 2: SK-N-SH
# Plate 4: K562 b (1 mL) - no one was around to consult on whether I should pellet the 2mL and replate
# Plate 4: K562 b (1 mL) - no one was around to consult on whether I should pellet the 2mL and replate
Wells (for all plates) - added 400 μL virus
# well 1 - GFP
# well 2 - KAH160/015 (2010)
# well 3 - KAH160/015 (2014)
# well 4 - KAH165/015 (2010)
# well 6 - KAH165/015 (2014)
# well 7 - KAH170/015 (2014)


Abbreviated protocol (from Seron Eaton)
Abbreviated protocol (from Seron Eaton)
* Add
* Retrieve frozen aliquots of harvested virus from -80C freezer (just outside TC room)
* Thaw and quick-spin to get virus off of the inside of lid
* Biohazard set-up: 10 mL Wescodyne waste conical (50 mL), 10 mL Wescodyne rinse





Revision as of 06:40, 28 September 2014

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09/23/14

  • Transductions: U2OS, SK-N-SH, K562

Transductions
Note: cells are in standard complete medium

  1. Plate 1: U2OS
  2. Plate 2: SK-N-SH
  3. Plate 4: K562 b (1 mL) - no one was around to consult on whether I should pellet the 2mL and replate

Wells (for all plates) - added 400 μL virus

  1. well 1 - GFP
  2. well 2 - KAH160/015 (2010)
  3. well 3 - KAH160/015 (2014)
  4. well 4 - KAH165/015 (2010)
  5. well 6 - KAH165/015 (2014)
  6. well 7 - KAH170/015 (2014)

Abbreviated protocol (from Seron Eaton)

  • Retrieve frozen aliquots of harvested virus from -80C freezer (just outside TC room)
  • Thaw and quick-spin to get virus off of the inside of lid
  • Biohazard set-up: 10 mL Wescodyne waste conical (50 mL), 10 mL Wescodyne rinse