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PEI Transfection

更新時(shí)間:2015-12-25      點(diǎn)擊次數(shù):4328

PEI Transfection

 

 

Transfection:

 

  1. Split 293T cells one day before transfection in DMEM/10% FBS medium:
    1. 6 well dish: 0.5x106 cells
    2. 10cm dish: 4.0x106 cells
    3. 15cm dish: 9.0x106 cells

 

  1. Prior to transfection bring all reagents to room temperature.

 

  1. In a sterile tube dilute total plasmid DNA (ug) in serum-free DMEM w/o phenol red (volume of media is 10% of final volume in culture vessel). Use transgene: viral packaging (psPAX2):viral envelope (pMD2G) constructs at 4:2:1 DNA ratio

 

  1. 6 well dish: 200ul + 3 ug of total DNA
  2. 10cm dish: 1mL + 7-8 ug of total DNA
  3. 15cm dish: 2mL +  11-12 ug of total DNA

 

  1. Add PEI (1ug/uL) to the diluted DNA. Mix immediay by vortexing or pipeting. The volume of PEI used is based on a 3:1 ratio of PEI (ug):total DNA (ug).

 

  1. 6 well dish: 9ul of PEI(1ug/ul) = 9ug
  2. 10cm dish: 21ul of PEI (1ug/ul) = 21ug
  3. 15cm dish: 33ul of PEI(1ug/ul) = 33ug

 

  1. Incubate 15 minutes at RT
  2. Add DNA/PEI mixture to cells

 

  1. Harvest transfected cells and/or viral supernatant at 48 hours post-transfection

 

 

Reagents:

 

PEI (1ug/ul) – PEI is Polyethylenimine 25kD linear from Polysciences (cat# 23966-2). To make a stock solution:

  • Dissolve PEI in endotoxin-free dH2O that has been heated to ~80°C.
  • Let cool to room temperature.
  • Neutralize to pH 7.0, filter sterilize (0.22um), aliquot and store at -20°C; a working stock can be kept at 4°C.
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    23966-2POLYETHYLENIMINE LINEAR28642 gpolysciences大量現(xiàn)貨
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    78002qf01線(xiàn)性PEI轉(zhuǎn)染液2001ml78bio23966配制
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    78004qf01POLYETHYLENIMINE LINEAR14321g78bio23966分裝
    78005qf01POLYETHYLENEIMINE 'MAX'(40 000M.W.*15921g78bio24765分裝
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