NBS1 Antibody

Mutations in NBS1 (Nijmegen Breakage Syndrome 1), also known as nibrin, are associated with the autosomal recessive syndrome, Nijmegen breakage syndrome, characterized by microcephaly, growth retardation, immunodeficiency, and cancer predisposition. At the cellular level, NBS1 is part of the MRE11/RAD50 double-strand break repair complex that is critical to the DNA damage response, DNA recombination, telomere integrity, and cell cycle checkpoint control.

Alternative names for NBS1 Antibody include cell cycle regulatory protein p95 antibody, NBS antibody, NBN antibody, ATV antibody, AT-V1 antibody, AT-V2 antibody, FLJ10155 antibody, MGC87362 antibody.