NBN Mouse anti-Human, Clone: 1D7, Abnova™
Mouse monoclonal antibody raised against full length recombinant human NBN.
Manufacturer: Abnova Corporation MAB12925
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]
|Mouse monoclonal antibody raised against full length recombinant human NBN.|
|Store at 4°C. For long term storage store at -20°C.
Aliquot to avoid repeated freezing and thawing.
|Immunohistochemistry (PFA fixed), Immunoprecipitation, Western Blot|
|Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) (5 ug/mL) Immunoprecipitation Western Blot The optimal working dilution should be determined by the end user.|
|Recombinant protein corresponding to full length human NBN.|
|Protein G purification|
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