PARVB Antibody (N-term) Blocking peptide
€363.00
In stock
SKU
AC-BP11774a
Background:
Mutations in this gene are associated with Nijmegenbreakage syndrome, an autosomal recessive chromosomal instabilitysyndrome characterized by microcephaly, growth retardation,immunodeficiency, and cancer predisposition. The encoded protein isa member of the MRE11/RAD50 double-strand break repair complexwhich consists of 5 proteins. This gene product is thought to beinvolved in DNA double-strand break repair and DNA damage-inducedcheckpoint activation.
Other Names:
Beta-parvin, Affixin, PARVB
Gene Name: PARVB
Gene ID: 29780
Primary Accession: Q9HBI1
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
Mutations in this gene are associated with Nijmegenbreakage syndrome, an autosomal recessive chromosomal instabilitysyndrome characterized by microcephaly, growth retardation,immunodeficiency, and cancer predisposition. The encoded protein isa member of the MRE11/RAD50 double-strand break repair complexwhich consists of 5 proteins. This gene product is thought to beinvolved in DNA double-strand break repair and DNA damage-inducedcheckpoint activation.
Other Names:
Beta-parvin, Affixin, PARVB
Gene Name: PARVB
Gene ID: 29780
Primary Accession: Q9HBI1
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
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