Chromatin-immunoprecipitation (ChIP) is a powerful technique for mapping the protein-DNA interactions that occur in living cells. The critical technical determinant for successful ChIP is the availability of an appropriate, "ChIP-grade" serum. Here we present a technique designed to assess whether sera are suitable for ChIP, and to quantify their efficiency relative to a positive internal reference. This approach is useful as a first step toward ChIP-on-chip or ChIP-sequencing, especially in the case of recently identified proteins for which no binding sites are yet known.
机构:
Fox Chase Canc Ctr, Program Cell & Dev Biol, WW Smith Chair Canc Res, Philadelphia, PA 19111 USAFox Chase Canc Ctr, Program Cell & Dev Biol, WW Smith Chair Canc Res, Philadelphia, PA 19111 USA
Chaya, D
Zaret, KS
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机构:
Fox Chase Canc Ctr, Program Cell & Dev Biol, WW Smith Chair Canc Res, Philadelphia, PA 19111 USAFox Chase Canc Ctr, Program Cell & Dev Biol, WW Smith Chair Canc Res, Philadelphia, PA 19111 USA