NBN antibody (clone 30000), anti-human
€435.00
In stock
SKU
AC-AT2976a
Catalog Number: AC-AT2976a
Size: 100 µg
Isotype: mouse IgG2a Kappa
Applications: WB, E
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Size: 100 µg
Isotype: mouse IgG2a Kappa
Applications: WB, E
Request Information AC-AT2976a">Request Information
Background:
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.
Other Names:
Nibrin, Cell cycle regulatory protein p95, Nijmegen breakage syndrome protein 1, NBN, NBS, NBS1, P95
Antigen Type:
Recombinant Protein
Gene Name: NBN (HGNC:7652)
Gene ID: 4683
NCBI Accession: NP_002476.2
Primary Accession: O60934
Other Accession: NM_002485
Format: Clear, colorless solution in phosphate buffered saline, pH 7.2 .
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.
Other Names:
Nibrin, Cell cycle regulatory protein p95, Nijmegen breakage syndrome protein 1, NBN, NBS, NBS1, P95
Antigen Type:
Recombinant Protein
Gene Name: NBN (HGNC:7652)
Gene ID: 4683
NCBI Accession: NP_002476.2
Primary Accession: O60934
Other Accession: NM_002485
Format: Clear, colorless solution in phosphate buffered saline, pH 7.2 .
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