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SH2 Domain Containing 1A (SH2D1A) Peptide

SH2D1A Reactivité: Mammifères Hôte: Synthetic BP, WB, IHC
N° du produit ABIN936059

Aperçu rapide pour SH2 Domain Containing 1A (SH2D1A) Peptide (ABIN936059)

Antigène

SH2D1A (SH2 Domain Containing 1A (SH2D1A))

Origine

Mammifères

Source

  • 7
Synthetic

Application

Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
  • Type de proteíne

    Synthetic

    Séquence

    YFRKIKNLIS AFQKPDQGIV IPLQYPVEKK SSARSTQGTT GIREDPDVCL

    Attributs du produit

    A synthetic peptide for use as a blocking control in assays to test for specificity of SH2 D2 antibody,
    Alternative Names: SH2D1A control peptide, SH2D1A antibody Blocking Peptide, Anti-SH2D1A Blocking Peptide, SH2 domain protein 1A Blocking Peptide, DSHP Blocking Peptide, EBVS Blocking Peptide, FLJ18687 Blocking Peptide, FLJ92177 Blocking Peptide, IMD5 Blocking Peptide, LYP Blocking Peptide, MTCP1 Blocking Peptide, SAP Blocking Peptide, XLP Blocking Peptide, XLPD Blocking Peptide, SH2D1A, SHD1A-2, SHD1A 2, SHD1A-2 Blocking Peptide, SHD1A 2 Blocking Peptide
  • Indications d'application

    Optimal conditions should be determined by the investigator

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Add 100 µL of distilled water for a final peptide concentration is 1 mg/mL.

    Buffer

    PBS

    Conseil sur la manipulation

    Avoid repeated freeze/thaw cycles.

    Stock

    -20 °C

    Stockage commentaire

    Store at -20 °C long term.
  • Antigène

    SH2D1A (SH2 Domain Containing 1A (SH2D1A))

    Sujet

    SH2D1A is a protein that plays a major role in the bidirectional stimulation of T and B cells. 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 SH2D1A 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.

    Poids moléculaire

    14 kDa
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