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NBS1 is a member of the MRE11/RAD50 double-strand break repair complex. Involved in DNA double-strand break repair and DNA damage-induced checkpoint activation. Mutation results in the Nijmegen breakage syndrome (NBS), an autosomal recessive chromosomal instability syndrome.

推荐稀释比 WB: 1/500-1/1000  IF: 1/50-1/200  IP: 1/50

Western

Western blot analysis of p95/NBS1 Phosphorylation in Jurkat lysates treated with Etopside using Phospho-p95 (Ser343) antibody.

-25 ~ -15℃保存，收到货之后有效期1年，避免反复冻融。