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Recombinant Rabbit Anti-ZAP70 Monoclonal Antibody
Recombinant Rabbit Anti-ZAP70 Monoclonal Antibody
ADMIO2; IMD48; SRK; STCD; STD; TZK; ZAP-70; mrtle; mur; ZAP70_HUMAN; ZAP70; 70 kDa zeta-chain associated protein; Syk-related tyrosine kinase; 2.7.10.2; ZAP70_MOUSE; zeta chain of T cell receptor associated protein kinase 70; tyrosine-protein kinase ZAP-7
Total $295.0
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Regular members: $236.0
  • NO.:SLA0712M
    concentration:1mg/ml
    React Species:Human, Mouse
    Immunogen Species:Mouse
    Clonality:Monoclonal
    Applications:WB, IHC-P, IHC-F, IF, ELISA
    Gene name:ZAP70
    UniProt Entry:P43403
    NCBI Gene Entry:7535
  • Goods click count:15
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Product NameRecombinant Rabbit Anti-ZAP70 Monoclonal Antibody
Cat No.SLA0712M
Chinese Namezeta相关蛋白70单克隆抗体
AliasADMIO2; IMD48; SRK; STCD; STD; TZK; ZAP-70; mrtle; mur; ZAP70_HUMAN; ZAP70; 70 kDa zeta-chain associated protein; Syk-related tyrosine kinase; 2.7.10.2; ZAP70_MOUSE; zeta chain of T cell receptor associated protein kinase 70; tyrosine-protein kinase ZAP-70
Host SpeciesMouse
IsotypeIgG1
ClonalityMonoclonal
Clone No.H5F1
React SpeciesHuman,Mouse
ApplicationsWB (1:500-2000)
IHC-P (1:100-500)
IHC-F (1:100-500)
IF (1:100-500)
ELISA (1:5000-10000)
Not yet tested in other applications.
Optimal working dilutions must be determined by the end user.
ImmunogenRecombinant human ZAP70 (Fragment) (His-tagged).
Purificationaffinity purified by Protein G
Concentration1mg/ml
Predicted MW.68 kDa
Subcellular LocationCytoplasm
Gene ID7535
Swiss-ProtP43403
Storage0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
BackgroundThis 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].
AttentionThis product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

 

FOR RESEARCH USE ONLY. Not for use in diagnostic or therapeutic procedures.

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