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NBN Rabbit anti-Human, Polyclonal Antibody, Abnova™

Rabbit polyclonal antibody raised against synthetic peptide of NBN.

Supplier:  Abnova Corporation PAB26645

Catalog No. 89-128-282


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Description

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

Sequence: S-L-Sp-Q-G
Specifications

Specifications

NBN
Polyclonal
Unconjugated
Western Blot (1:500-1:1000) Immunohistochemistry (1:50-1:100) The optimal working dilution should be determined by the end user.
NBN
NBN
A synthetic peptide corresponding to residues surrounding S343 of human NBN.
100 μg
Primary
Human
Liquid
Immunohistochemistry (PFA fixed), Western Blot
1 mg/mL
Rabbit polyclonal antibody raised against synthetic peptide of NBN.
In PBS (without Mg2+ and Ca2+), 150mM NaCl, pH 7.4 (50% glycerol, 0.02% sodium azide)
AT-V1/AT-V2/ATV/FLJ10155/MGC87362/NBS/NBS1/P95
Rabbit
Affinity chromatography
RUO
4683
Store at -20°C.
Aliquot to avoid repeated freezing and thawing.
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