|Application ||WB, E|
|Calculated MW||74123 Da|
|Antigen Region||313-340 aa|
|Other Names||Ubiquitin-associated and SH3 domain-containing protein A, Cbl-interacting protein 4, CLIP4, Suppressor of T-cell receptor signaling 2, STS-2, T-cell ubiquitin ligand 1, TULA-1, UBASH3A, STS2|
|Target/Specificity||This UBASH3A antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 313-340 amino acids from the Central region of human UBASH3A.|
|Format||Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification.|
|Storage||Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.|
|Precautions||UBASH3A Antibody (Center) is for research use only and not for use in diagnostic or therapeutic procedures.|
|Function||Interferes with CBL-mediated down-regulation and degradation of receptor-type tyrosine kinases. Promotes accumulation of activated target receptors, such as T-cell receptors, EGFR and PDGFRB, on the cell surface. Exhibits negligigle protein tyrosine phosphatase activity at neutral pH. May act as a dominant-negative regulator of UBASH3B-dependent dephosphorylation. May inhibit dynamin-dependent endocytic pathways by functionally sequestering dynamin via its SH3 domain.|
|Cellular Location||Cytoplasm. Nucleus.|
|Tissue Location||Highest expression of UBASH3A in tissues belonging to the immune system, including spleen, peripheral blood leukocytes, thymus and bone marrow.|
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Provided below are standard protocols that you may find useful for product applications.
UBASH3A interferes with CBL-mediated down-regulation and degradation of receptor-type tyrosine kinases. Promotes accumulation of activated target receptors, such as T-cell receptors, EGFR and PDGFRB, on the cell surface.
Hinks, A., et al. Ann. Rheum. Dis. (2010) In press :
Stahl, E.A., et al. Nat. Genet. 42(6):508-514(2010)
Jin, Y., et al. N. Engl. J. Med. 362(18):1686-1697(2010)
Barrett, J.C., et al. Nat. Genet. 41(6):703-707(2009)
Smyth, D.J., et al. N. Engl. J. Med. 359(26):2767-2777(2008)
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