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BRAF antibody (AA 299-447)

This anti-BRAF antibody is a Mouse Monoclonal antibody detecting BRAF in WB, ELISA, IHC and FACS. Suitable for Human and Rat.
Catalog No. ABIN7193853

Quick Overview for BRAF antibody (AA 299-447) (ABIN7193853)

Target

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

Reactivity

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Human, Rat

Host

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Mouse

Clonality

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Monoclonal

Conjugate

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This BRAF antibody is un-conjugated

Application

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Western Blotting (WB), ELISA, Immunohistochemistry (IHC), Flow Cytometry (FACS)

Clone

2A10D7
  • Binding Specificity

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    AA 299-447

    Purpose

    BRAF Antibody

    Purification

    Purified antibody

    Immunogen

    Purified recombinant fragment of human BRAF (AA: 299-447) expressed in HEK293-6e.

    Isotype

    IgG1
  • Application Notes

    ELISA: 1/10000

    FCM: 1/200 - 1/400

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified antibody in PBS with 0.05 % 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,-20 °C

    Storage Comment

    Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
  • Target

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

    Alternative Name

    BRAF

    Background

    This gene encodes a protein belonging to the RAF family of serine/threonine protein kinases. This protein plays a role in regulating the MAP kinase/ERK signaling pathway, which affects cell division, differentiation, and secretion. Mutations in this gene, most commonly the V600E mutation, are the most frequently identified cancer-causing mutations in melanoma, and have been identified in various other cancers as well, including non-Hodgkin lymphoma, colorectal cancer, thyroid carcinoma, non-small cell lung carcinoma, hairy cell leukemia and adenocarcinoma of lung. Mutations in this gene are also associated with cardiofaciocutaneous, Noonan, and Costello syndromes, which exhibit overlapping phenotypes. A pseudogene of this gene has been identified on the X chromosome. [provided by RefSeq, Aug 2017]

    Molecular Weight

    84.4 kDa

    Gene ID

    673

    UniProt

    P15056

    Pathways

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