How to re-amplify the DDRT-PCR band?
lha at med.pitt.edu
Fri Mar 14 10:52:22 EST 1997
In article <199703140250.KAA20930 at public3.bta.net.cn>,
nhwu at PUBLIC3.BTA.NET.CN wrote:
> Dear netters,
> I pleased my boss by good result of Differential Display. But I cannot
> re-amplify the band I interest in.
Here's the protocol we use: (Maniatis 6.46) The crush and soak technique.
Make elution buffer: Ammonium acetate 0.5 M, Mg acetate 10 mM, EDTA 1mM,
SDS 0.1%. Excise gel piece, crush it in 50-100 ul of elution buffer.
Incubate at 37C for 4 hrs, then centrifuge 12,000g x 1 min, recover
supernatant. Add another 50 ul of elution buffer to pellet, votex,
centrifuge, combine supernatants. Filter the elution through glass wool
to remove large particles, then Etoh precipitate and wash. Bring up in a
small volume (10 ul) of TE Buffer. Re-amplify using the same PCR
conditions and primers as DD-PCR.
U of Pittsburgh
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