bs-20442R [Primary Antibody]
Rabbit  Anti-Phospho-BRCA1 (Ser1466)  Polyclonal Antibody
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Host: Rabbit

Target Protein: Phospho-BRCA1 (Ser1466)

IR: Immunogen Range:PI(p-S)QN

Clonality: Polyclonal

Isotype: IgG

Entrez Gene: 672

Swiss Prot: P38398

Source: KLH conjugated synthesised phosphopeptide derived from human BRCA1 around the phosphorylation site of Ser1466:PI(p-S)QN 

Purification: affinity purified by Protein A

Storage: 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol. Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.

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. Many alternatively spliced transcript variants, some of which are disease-associated mutations, have been described for this gene, but the full-length natures of only some of these variants has been described. A related pseudogene, which is also located on chromosome 17, has been identified. [provided by RefSeq, May 2009].

Size: 100ul

Concentration: 1mg/ml

Applications: IHC-P=1:100-500, IHC-F=1:100-500, ICC=1:100-500, IF=1:100-500, Flow-Cyt=1μg/Test, ELISA=1:5000-10000

Cross Reactive Species: Human (predicted: Horse)

For research use only. Not intended for diagnostic or therapeutic use.

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