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BRAF antibody (AA 25-75)

This anti-BRAF antibody is a Rabbit Polyclonal antibody detecting BRAF in WB, IP and IHC (fp). Suitable for Human.
Catalog No. ABIN7454774

Quick Overview for BRAF antibody (AA 25-75) (ABIN7454774)

Target

See all BRAF Antibodies
BRAF (B-Raf proto-oncogene, serine/threonine kinase (BRAF))

Reactivity

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  • 69
  • 49
  • 5
  • 5
  • 3
  • 2
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  • 1
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Human

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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  • 8
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This BRAF antibody is un-conjugated

Application

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Western Blotting (WB), Immunoprecipitation (IP), Immunohistochemistry (Formalin-fixed Paraffin-embedded Sections) (IHC (fp))
  • Binding Specificity

    • 18
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    AA 25-75

    Purpose

    Rabbit anti-BRAF Antibody, Affinity Purified

    Predicted Reactivity

    Mouse

    Purification

    Affinity Purified

    Immunogen

    between AA 25 and 75

    Isotype

    IgG
  • Application Notes

    IHC: 1:200 - 1:1,000. Epitope retrieval with citrate buffer pH 6.0 is recommended for FFPE tissue sections.

    IP: 2 - 5 μg/mg lysate

    WB: 1:2,000 - 1:10,000

    Restrictions

    For Research Use only
  • Concentration

    200 μg/mL

    Buffer

    Tris-buffered Saline containing 0.1 % BSA and 0.09 % Sodium Azide

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    4 °C

    Expiry Date

    12 months
  • Target

    BRAF (B-Raf proto-oncogene, serine/threonine kinase (BRAF))

    Alternative Name

    BRAF

    Background

    Background: B-Raf proto-oncogene serine/threonine-protein kinase (BRAF) is a member of the raf/mil family of serine/threonine kinases. BRAF is involved in transducing mitogenic signals via the MAP kinase/ERKs signaling pathway. Mutations in BRAF are involved in a wide range of cancers such as lung, non-Hodgkin lymphoma, and colorectal cancer. Defects in BRAF are also the cause of cardiofaciocutaneous syndrome (CFC), an autosomal dominant syndrome characterized by facial anomalies, heart defects, and ectodermal abnormalities.

    Gene ID

    673

    NCBI Accession

    NP_004324

    UniProt

    P15056

    Pathways

    MAPK Signaling, RTK Signaling, Neurotrophin Signaling Pathway, Ribonucleoprotein Complex Subunit Organization, Hepatitis C, Autophagy
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