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SH2D1A antibody

This anti-SH2D1A antibody is a Rabbit Polyclonal antibody detecting SH2D1A in WB, ELISA and IHC. Suitable for Human, Mouse and Rat.
Catalog No. ABIN7119006

Quick Overview for SH2D1A antibody (ABIN7119006)

Target

See all SH2D1A Antibodies
SH2D1A (SH2 Domain Containing 1A (SH2D1A))

Reactivity

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  • 1
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Human, Mouse, Rat

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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  • 1
  • 1
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  • 1
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This SH2D1A antibody is un-conjugated

Application

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Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
  • Purification

    Immunogen affinity purified

    Purity

    ≥95 % as determined by SDS-PAGE

    Immunogen

    SH2 domain protein 1A

    Isotype

    IgG
  • Application Notes

    WB: 1:500 - 1:2000, IHC: 1:50 - 1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide and 50 % glycerol pH 7.3 ,

    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

    -20 °C

    Storage Comment

    -20°C for 12 months (Avoid repeated freeze / thaw cycles.)

    Expiry Date

    12 months
  • Target

    SH2D1A (SH2 Domain Containing 1A (SH2D1A))

    Alternative Name

    SH2D1A

    Background

    Synonyms:DSHP, SAP Background:This gene encodes a protein that plays a major role in the bidirectional stimulation of T and B cells. This protein contains an SH2 domain and a short tail. It associates with the signaling lymphocyte-activation molecule, thereby acting as an inhibitor of this transmembrane protein by blocking the recruitment of the SH2-domain-containing signal-transduction molecule SHP-2 to its docking site. This protein can also bind to other related surface molecules that are expressed on activated T, B and NK cells, thereby modifying signal transduction pathways in these cells. Mutations in this gene cause lymphoproliferative syndrome X-linked type 1 or Duncan disease, a rare immunodeficiency characterized by extreme susceptibility to infection with Epstein-Barr virus, with symptoms including severe mononucleosis and malignant lymphoma. Multiple transcript variants encoding different isoforms have been found for this gene.

    Molecular Weight

    17 kDa

    Gene ID

    4068

    UniProt

    O60880

    Pathways

    Regulation of Leukocyte Mediated Immunity, Positive Regulation of Immune Effector Process
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