ZAP70 antibody (pTyr493) (Cy5)
Quick Overview for ZAP70 antibody (pTyr493) (Cy5) (ABIN746952)
Target
See all ZAP70 AntibodiesReactivity
Host
Clonality
Conjugate
Application
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Binding Specificity
 - pTyr493
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Predicted Reactivity
 - Human,Mouse,Rat,Cow,Pig,Horse,Rabbit
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Purification
 - Purified by Protein A.
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Immunogen
 - KLH conjugated synthetic phosphopeptide derived from human Zap-70 around the phosphorylation site of Tyr493
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Isotype
 - IgG
 
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Application Notes
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                        FCM 1:20-100
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 - 
                                            
Restrictions
 - For Research Use only
 
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Format
 - Liquid
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Concentration
 - 1 μg/μL
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Buffer
 - Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
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Preservative
 - ProClin
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Precaution of Use
 - This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
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Storage
 - -20 °C
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Storage Comment
 - Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
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Expiry Date
 - 12 months
 
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- ZAP70 (zeta-Chain (TCR) Associated Protein Kinase 70kDa (ZAP70))
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Alternative Name
 - ZAP70
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Background
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Synonyms: Zap-70Tyr493, ZAP70 phospho Y493, p-ZAP70 Y292, p-Zap-70Tyr292, p-Zap-70Y292, ZAP-70, ZAP 70, ZAP70, zeta-associated protein 70, ZAP-70=protein tyrosine kinase Syk homolog {SH2-like and C-terminal kinase domains}, Tyrosine-protein kinase ZAP-70, 70 kDa zeta-associated protein, Syk-related tyrosine kinase. SRK, STD, TZK, ZAP70_HUMAN, Tyrosine-protein kinase ZAP-70, 70 kDa zeta-chain associated protein.
Background: This gene encodes an enzyme belonging to the protein tyrosine kinase family, and it plays a role in T-cell development and lymphocyte activation. This enzyme, which is phosphorylated on tyrosine residues upon T-cell antigen receptor (TCR) stimulation, functions in the initial step of TCR-mediated signal transduction in combination with the Src family kinases, Lck and Fyn. This enzyme is also essential for thymocyte development. Mutations in this gene cause selective T-cell defect, a severe combined immunodeficiency disease characterized by a selective absence of CD8-positive T-cells. Two transcript variants that encode different isoforms have been found for this gene. [provided by RefSeq, Jul 2008].
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Gene ID
 - 7535
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Pathways
 - TCR Signaling, Ubiquitin Proteasome Pathway
 
Target
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