特徴
- Background:nibrin(NBN) Homo sapiens 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, Jul 2008],
仕様
- サイズ:100ul
- Source:Rabbit
- Applications:WB,IHC-p,ELISA
- Species reactivity:Human,Rat
- Immunogen:The antiserum was produced against synthesized peptide derived from human p95/NBS1. AA range:310-359
- Purification:The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
- Concentration:1 mg/ml
- Observed band:85
- GeneID(Human):NBN
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商品のバリエーション (サイズ違い・スペック違い・オプション品など)
| 商品イメージ | アズワン品番 商品名 |
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86-7714-01
Nibrin Polyclonal Antibody 100ul
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86-7714-88
Nibrin Polyclonal Antibody 100ul
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86-7713-99
Nibrin Polyclonal Antibody 100ul
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