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BRCA1 Polyclonal Antibody Store at -20°C
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BRCA1 Polyclonal Antibody Store at -20°C

SKU: E-AB-10188-200

  • $ 33995
  • Save $ 6000



BRCA1 Polyclonal Antibody Store at -20°C

 

SKU # E-AB-10188
Reactivity Human
Host Rabbit
Applications IHC

 

Product Details

Isotype IgG
Host Rabbit
Reactivity Human
Applications IHC
Clonality Polyclonal
Immunogen Recombinant protein of human BRCA1
Abbre BRCA1
Synonyms BRCA 1,  BRCA1,  BRCA1 DNA repair associated,  BRCA1/BRCA2 containing complex subunit 1,  BRCA1/BRCA2-containing complex,  BRCAI,  BRCC 1,  BRCC1,  Breast Cancer 1,  Breast Cancer 1 Early Onset,  Breast and ovarian cancer susceptibility protein 1,  Breast cance,  subunit 1
Swissprot
Cellular Localization Cytoplasm, Nucleus, Localizes at sites of DNA damage at double-strand breaks (DSBs) and recruitment to DNA damage sites is mediated by the BRCA1-A complex.
Concentration 0.3 mg/mL
Buffer Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol.
Purification Method Affinity purification
Research Areas Cancer,  Cell Biology,  Epigenetics and Nuclear Signaling
Conjugation Unconjugated
Storage Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.
Shipping The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended.

 

Related Reagents

Applications Recommended Dilution
IHC 1:50-1:200

 

Background

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.