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NBN Rabbit anti-Human, Polyclonal Antibody, Abnova™
Rabbit polyclonal antibody raised against synthetic peptide of NBN.
Brand: Abnova PAB24951.100uL
Description
Mutations in this gene are associated with Nijmegen breakage syndrome, an autosomal recessive chromosomal instability syndrome characterized by microcephaly, growth retardation, immunodeficiency, and cancer predisposition. The encoded protein is a member of the MRE11/RAD50 double-strand break repair complex which consists of 5 proteins. This gene product is thought to be involved in DNA double-strand break repair and DNA damage-induced checkpoint activation. [provided by RefSeq
Specifications
| NBN | |
| Polyclonal | |
| Unconjugated | |
| Western Blot (1:500-1:1000) Immunofluorescence (1:50-1:200) The optimal working dilution should be determined by the end user. | |
| NBN | |
| NBN | |
| A synthetic peptide corresponding to NBN. | |
| 100 μL | |
| Primary | |
| NBN polyclonal antibody detects endogenous levels of NBN protein. | |
| Store at 4°C. For long term storage store at -20°C. Aliquot to avoid repeated freezing and thawing. |
| Immunofluorescence, Western Blot | |
| 1 mg/mL | |
| Rabbit polyclonal antibody raised against synthetic peptide of NBN. | |
| In PBS, pH 7.2 (0.05% sodium azide) | |
| AT-V1/AT-V2/ATV/FLJ10155/MGC87362/NBS/NBS1/P95 | |
| Rabbit | |
| Antigen affinity purification | |
| RUO | |
| 4683 | |
| Human | |
| Liquid |
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