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.
Nbn
nibrin
:  ATV AT-V1 AT-V2 cell cycle regulatory protein p95 NBS Nbs1 Nijmegen breakage syndrome 1 (nibrin) Nijmegen breakage syndrome protein 1 nijmegen breakage syndrome protein 1 homolog P95 p95 protein of the MRE11/RAD50 complex
Product
Specifications
Ordering Information
Human
WB, IP
Between 625 and 675
100
$339
$229
$99
Mouse
WB, IP
Between 701 and 751
100
$339
$229
$99
Human
WB, IP, IHC-P
Between 425 and 475
100
$339
$229
$99
Human
WB, IP, IHC-P, PLA
Between 704 and 754
100
$339
$229
$99
Human, Mouse
100
Includes: 1 each of A300-187A, A301-284A, A301-289A and A301-290A
$937
Includes: 1 each of A300-187A, A301-284A, A301-289A and A301-290A
Human
IHC-P, IF
Between 704 and 754
100
$360
$99