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in vitro Transcription

来源:本站原创  2006/8/3 7:35:00   访问量:4809
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in vitro Transcription

Reaction

  • 1 µl 10X Transcription Buffer (Ambion)
  • 1 µl 10X NTPs (4 mM ATP, CTP, 1 mM GTP, UTP)
  • 2 µl 10 mM GpppG cap (Pharmacia)
  • 2 µl a[32P]-UTP (NEN) 800 Ci/mmol
  • 0.2 µl RNasin (Promega)
  • 1 µl 0.1M DTT
  • 1.8 µl H2O
  • 0.5 µl Linearized Transcription Template (1 µg/µl)
  • 0.5 µl Polymerase (SP6/T7/T3)

 

Incubate for 1 hour at 37°C.

Add 10 µl STOP solution (formamide loading buffer) to each reaction, boil, and load onto a pre-run 5% denaturing polyacrylamide gel.

Run desired distance.

Cut out bands and soak in 500 µl RNA elution buffer (300 mM NaOAc, pH 6.1, 0.2% SDS, 1 mM EDTA) for 1 hour - overnight

Precipitate RNA with 2 volumes ethanol.

Resuspend in 20 µl H2O and quantitate 0.5 µl.

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