89-115-682

BRCA1 (phospho S988), Rabbit anti-Human, Polyclonal Antibody, Abnova™

Manufacturer: Abnova Corporation

Select a Size

Pack Size SKU Availability Price
Each of 1 89-115-682-Each-of-1 In Stock ₹ 57,138.00

89-115-682 - Each of 1

₹ 57,138.00

In Stock

Quantity

1

Base Price: ₹ 57,138.00

GST (18%): ₹ 10,284.84

Total Price: ₹ 67,422.84

Antigen

BRCA1

Classification

Polyclonal

Description

Rabbit polyclonal antibody raised against synthetic phosphopeptide of BRCA1.

Formulation

In PBS (without mg2+and Ca2+), 150mM NaCl, pH 7.4 (50% glycerol, 0.02% sodium azide)

Gene Accession No.

P38398

Gene Symbols

BRCA1

Immunogen

Synthetic phosphopeptide (conjugated with KLH) corresponding to residues surrounding S988 of human BRCA1.

Regulatory Status

RUO

Gene ID (Entrez)

672

Target Species

Human

Form

Liquid

Applications

Immunofluorescence

Conjugate

Unconjugated

Dilution

Immunofluorescence (1:100-1:200) The optimal working dilution should be determined by the end user.

Gene

BRCA1

Gene Alias

BRCAI/BRCC1/IRIS/PSCP/RNF53

Host Species

Rabbit

Quantity

100 μL

Primary or Secondary

Primary

Test Specificity

BRCA1 (phospho-Ser988) antibody detects endogenous levels of BRCA1 only when phosphorylated at serine 988.

Content And Storage

Store at -20°C.Aliquot to avoid repeated freezing and thawing.

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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
  • 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 Sequence: IKSpFV