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BRCA1 antibody (AA 445-620)

This anti-BRCA1 antibody is a Mouse Monoclonal antibody detecting BRCA1 in IF, IHC (p) and FACS. Suitable for Human.
Catalog No. ABIN4949483

Quick Overview for BRCA1 antibody (AA 445-620) (ABIN4949483)

Target

See all BRCA1 Antibodies
BRCA1 (Breast Cancer 1 (BRCA1))

Reactivity

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Human

Host

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Mouse

Clonality

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Monoclonal

Conjugate

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This BRCA1 antibody is un-conjugated

Application

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Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Flow Cytometry (FACS)

Clone

BRCA1-1398
  • Binding Specificity

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    AA 445-620

    Purification

    Protein G affinity chromatography

    Immunogen

    Amino acids 445-620 were used as the immunogen for the BRCA1 antibody.

    Isotype

    IgG1
  • Application Notes

    Optimal dilution of the BRCA1 antibody should be determined by the researcher.\. Flow Cytometry: 2-4 μg/million cells in 0.1ml,Immunofluorescence: 2-4 μg/mL,IHC (FFPE): 5-10 μg/mL

    Restrictions

    For Research Use only
  • Concentration

    1 mg/mL

    Buffer

    1 mg/mL in 1X PBS, BSA free, sodium azide free

    Preservative

    Azide free

    Storage

    4 °C,-20 °C

    Storage Comment

    Store the BRCA1 antibody at 2-8°C (with azide) or aliquot and store at -20°C or colder (without azide).
  • Target

    BRCA1 (Breast Cancer 1 (BRCA1))

    Alternative Name

    BRCA1

    Background

    BRCA1 (Breast cancer type 1 susceptibility protein) is 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.

    Pathways

    Cell Division Cycle, DNA Damage Repair, Intracellular Steroid Hormone Receptor Signaling Pathway, Positive Regulation of Response to DNA Damage Stimulus
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