Human ARHGAP32(Rho GTPase-activating protein 32)ELISA Kit

Starting at: $696.00

  • Model: ELI-14578h
  • 20 Units in Stock
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Human ARHGAP32 (Rho GTPase- activating protein 32) ELISA Kit (CUSTOM)

96 Tests

Operating instructions




Alternative name

Human Arhgap32 ELISA KIT ,Human GC-GAP ELISA KIT ,Human GRIT ELISA KIT ,Human PX-RICS ELISA KIT ,Human RICS ELISA KIT ,Human p200RhoGAP ELISA KIT ,Human p250GAP ELISA KIT ,Human GAB-associated CDC42 ELISA KIT ,Human GAB-associated Cdc42/Rac GTPase-activating protein ELISA KIT ,Human GTPase regulator interacting with TrkA ELISA KIT ,Human GTPase-activating protein for Cdc42 and Rac1 ELISA KIT ,Human RhoGAP involved in the -catenin-N-cadherin and NMDA receptor signaling ELISA KIT ,Human brain-specific Rho GTP-ase-activating protein ELISA KIT ,Human brain-specific Rho GTPase-activating protein ELISA KIT ,Human rac GTPase activating protein ELISA KIT ,Human rho-type GTPase-activating protein 32 ELISA KIT ,Human rho/Cdc42/Rac GTPase-activating protein RICS ELISA KIT ,Human rhoGAP involved in the beta-catenin-N-cadherin and NMDA receptor signaling ELISA KIT ,Human Rho GTPase activating protein 32 ELISA KIT


Intended use

Human ARHGAP32 ELISA kit allows for the in vitro quantitative determination of Human Rho GTPase- activating protein 32 concentrations in serum, plasma, tissue homogenates, cell culture supernates, and other biological fluids.


Test principle

Human ARHGAP32 ELISA kit is based on the competitive binding enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with an antibody specific to ARHGAP32, During the reaction, ARHGAP32 in the sample or standard competes with a fixed amount of biotin-labeled ARHGAP32 for sites on a pre-coated Monoclonal antibody specific to ARHGAP32. Excess conjugate and unbound sample or standard are washed from the plate. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then a TMB substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The concentration of ARHGAP32 in the samples is then determined by comparing the O.D. of the samples to the standard curve.

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