ELISA VASP-P

Principle

A microwell plate is coated with a specific mouse monoclonal antihuman VASP antibody that binds to VASP to be measured. Then, a peroxidase-coupled mouse anti-human VASP-P monoclonal antibody binds to phosphorylated serine 239 antigenic determinant of VASP. The bound enzyme peroxidase is then revealed by its activity on the TMB substrate over a predetermined time. After stopping the reaction, absorbance at 450 nm is directly related to the concentration of VASP-P initially contained in the sample.

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Presentation

Reference

CP013 & CP019

Sample 80 µL citrated  whole blood
Quantity 47 samples maximum
Detection

ELISA

Reagents PGE1, PGE1 + ADP, Lysis buffer, Coated plate, Washing solution, Dilution buffer, Anti-human VASP-P antibody –peroxidase, TMB, Stop solution.
Description Enzyme immunoassay of VASP-P.