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>   首页   >   产品   >   一抗   >   精选抗体   >   磷酸化抗体   >    Phosphotyrosine (P-Tyr) Antibody - With BSA and Azide   

Phosphotyrosine (P-Tyr) Antibody - With BSA and Azide

Mouse Monoclonal Antibody [Clone PY793 ]

     
  • 2 -  Phosphotyrosine (P-Tyr) Antibody - With BSA and Azide AH12985
    Formalin-fixed, paraffin-embedded human Breast Carcinoma stained with Phosphotyrosine Monoclonal Antibody (PY793).
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Product Information
Application
  • Applications Legend:
  • E=ELISA
  • WB=Western Blotting
  • IHC=Immunohistochemistry
  • IHC-P=Immunohistochemistry (Paraffin)
  • IP=Immunoprecipitation
  • IF=Immunofluorescence
  • IC=Immunochemistry
  • ICC=Immunocytochemistry
  • FC=Flow Cytometry
  • DB=Dot Blot
IHC, IF, FC
Host Mouse
Clonality Monoclonal
Isotype Mouse / IgG2b
Clone Names PY793
Calculated MW Depends upon the phosphorylated target
Additional Information
Application Note IHC~~1:100~500
IF~~1:50~200
FC~~1:10~50
StorageStore at 2 to 8°C.Antibody is stable for 24 months.
Precautions Phosphotyrosine (P-Tyr) Antibody - With BSA and Azide is for research use only and not for use in diagnostic or therapeutic procedures.
Research Areas

For Research Use Only. Not For Use In Diagnostic Procedures.

BACKGROUND

Protein phosphorylation is a fundamental event in the regulation of a large number of intracellular processes. Phosphorylation of specific tyrosine residues is the result of activation or stimulation of their respective protein tyrosine kinases. The phosphorylated proteins can be auto-phosphorylated kinases or certain cellular protein substrates. Tyrosine-phosphorylated proteins are involved in signal transduction and in the regulation of cell proliferation. Antibody to phosphotyrosine provides an excellent tool for the detection, characterization, and purification of phosphotyrosine containing proteins. This MAb shows no cross-reaction with other phosphoamino acids and is superb for multiple applications including staining of formalin/paraffin tissues.

REFERENCES

Hunter, T., et al. 1985. Protein-tyrosine kinases. Annu. Rev. Biochem. 54: 897-930

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