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NBN Mouse anti-Human, Clone:7E4C2, Abnova™
Mouse monoclonal antibody raised against recombinant human NBN.
Brand: Abnova MAB17791.100ug
This item is not returnable.
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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 | |
| Monoclonal | |
| Unconjugated | |
| ELISA (1:10000) Flow Cytometry (1:200-1:400) Immunocytochemistry (1:200-1:1000) Immunohistochemistry (1:200-1:1000) Western Blot (1:500-1:2000) The optimal working dilution should be determined by the end user. |
|
| NBN | |
| Mouse | |
| 100 μg | |
| Human | |
| Antibody | |
| IgG2a |
| ELISA, Flow Cytometry, Immunocytochemistry, Immunohistochemistry (Paraffin), Western Blot | |
| 7E4C2 | |
| nibrin | |
| In PBS (0.05% sodium azide) | |
| AT-V1, AT-V2, ATV, FLJ10155, MGC87362, NBS, NBS1, P95 | |
| Recombinant protein corresponding to amino acids 467-615 of human NBN from E. coli. | |
| 4683 | |
| Store at 4°C. For long term storage store at -20°C. Aliquot to avoid repeated freezing and thawing. |
|
| Liquid |
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