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Immunohistochemistry of paraffin-embedded Human liver cancer tissue using BRCA1 Polyclonal Antibody at dilution 1:35
Immunohistochemistry of paraffin-embedded Human liver cancer tissue using BRCA1 Polyclonal Antibody at dilution 1:35
Immunohistochemistry of paraffin-embedded Human liver cancer tissue using BRCA1 Polyclonal Antibody at dilution 1:35

BRCA1 Polyclonal Antibody

E-AB-10188
Elabscience
ApplicationsImmunoHistoChemistry
Product group Antibodies
TargetBRCA1
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Overview

  • Supplier
    Elabscience
  • Product Name
    BRCA1 Polyclonal Antibody
  • Delivery Days Customer
    12
  • Applications
    ImmunoHistoChemistry
  • Applications Supplier
    ELISA IHC
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    0.3 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID672
  • Target name
    BRCA1
  • Target description
    BRCA1 DNA repair associated
  • Target synonyms
    BRCAI, BRCC1, BROVCA1, FANCS, IRIS, PNCA4, PPP1R53, PSCP, RNF53, breast cancer type 1 susceptibility protein, BRCA1/BRCA2-containing complex, subunit 1, Fanconi anemia, complementation group S, RING finger protein 53, breast and ovarian cancer susceptibility protein 1, breast cancer 1, early onset, early onset breast cancer 1, protein phosphatase 1, regulatory subunit 53
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDP38398
  • Protein Name
    Breast cancer type 1 susceptibility protein
  • Scientific Description
    This gene encodes a nuclear phosphoprotein that plays a role in maintaining genomic stability, and it also acts as a tumor suppressor. The encoded protein combines with other tumor suppressors, DNA damage sensors, and signal transducers to form a large multi-subunit protein complex known as the BRCA1-associated genome surveillance complex (BASC). This gene product associates with RNA polymerase II, and through the C-terminal domain, also interacts with histone deacetylase complexes. This protein thus plays a role in transcription, DNA repair of double-stranded breaks, and recombination. Mutations in this gene are responsible for approximately 40% of inherited breast cancers and more than 80% of inherited breast and ovarian cancers. Alternative splicing plays a role in modulating the subcellular localization and physiological function of this gene.
  • Storage Instruction
    -20°C
  • UNSPSC
    41116161