SH2D1A Polyclonal Antibody

Rs. 21,832.00
SKU E-AB-60208


Synonyms DSHP,Duncan disease SH2 protein,Duncan disease SH2-protein,EBVS,IMD5,LYP,MTCP1,SAP,SAP/SH2D1A,SH2 domain containing 1A,SH2 domain protein 1A,SH2 domain-containing protein 1A,SH21A,SH2D1A,Signaling lymphocyte activation molecule associated protein,Signaling lymphocytic activation molecule-associated protein,SLAM associated protein,SLAM associated protein/SH2 domain protein 1A,SLAM-associated protein,T cell signal transduction molecule SAP,T-cell signal transduction molecule SAP,XLP,XLPD
Swissprot O60880
Source Rabbit
Reactivity Human,Mouse,Rat
Immunogen Recombinant protein of human SH2D1A
Application WB
Recommended dilution WB 1:500 - 1:2000
Concentration 1mg/ml
Clonality Polyclonal


Cellular localization  
Tissue specificity  
Isotype IgG
Purification Affinity purification
Conjugation Unconjugated
Storage instructions Store at -20℃. Avoid freeze / thaw cycles.
Storage buffer Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
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.


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