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Human CXCL1 / GRO alpha ELISA Kit

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Human CXCL1 / GRO alpha ELISA Kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human CXCL1 / GRO alpha in serum, plasma, tissue homogenates, and other biological fluids.

Applications:Sandwich ELISA, Host:, Reactivity:Human, Product range:15.625-1000 pg/ml, Sensitivity:9.375 pg/ml, Storage:Store at +4?C. Do not use past expiration date!, Target:CXCL1 / GRO alpha, Sample type:Serum, plasma, tissue homogenates, and other biological fluids, Principle assay:Human CXCL1 / GRO alpha ELISA Kit (A76393) employs the sandwich enzyme immunoassay technique for the quantitative measurement of human CXCL1 / GRO alpha in serum, plasma, tissue homogenates, and other biological fluids. An antibody specific for CXCL1 / GRO alpha has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the CXCL1 / GRO alpha present in each sample is bound to the wells by the immobilized antibody. Following incubation, the wells are washed and then incubated with Biotinylated Anti-CXCL1 / GRO alpha Antibody, which binds the captured CXCL1 / GRO alpha present in each well. Following incubation, unbound biotinylated detection antibody is removed by washing, and an HRP-Streptavidin conjugate is added to the wells and the microtiter plate is incubated. Following incubation and washing, TMB substrate solution is then used to visualize the HRP enzymatic reaction by catalysis to produce a blue-coloured product that changes to yellow after addition of acidic stop solution. The density of yellow is proportional to the amount of CXCL1 / GRO alpha captured in each well. The concentration of CXCL1 / GRO alpha can then be calculated by reading the O.D. absorbance at 450nm in a microplate reader and referring to the standard curve, Assay type:Sandwich (quantitative), Detection type:Colorimetric, Platform:Pre-coated Microplate (12 x 8 well strips), Assay time:4h 30m

+25° C.

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USA

BTN - HC

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