Human ACAT2/Acetyl-CoA Acetyltransferase ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human ACAT2/Acetyl-CoA Acetyltransferase in serum, plasma, tissue homogenates, and other biological fluids.

• Ready To Use ELISA Kit
• Detection Range: 78.125 to 5000 pg/ml
• Sensitivity: 46.875 pg/ml
• Sample Type: Serum, plasma, tissue homogenates, and other biological fluids
• Assay Precision: Intra - Assay: CV <8%, Inter - Assay: CV <10%

Human ACAT2 / Acetyl-CoA Acetyltransferase ELISA Kit (A75150) employs the sandwich enzyme immunoassay technique for the quantitative measurement of human ACAT2 / Acetyl-CoA Acetyltransferase in serum, plasma, tissue homogenates, and other biological fluids. An antibody specific for ACAT2 / Acetyl-CoA Acetyltransferase has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the ACAT2 / Acetyl-CoA Acetyltransferase 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-ACAT2 / Acetyl-CoA Acetyltransferase Antibody, which binds the captured ACAT2 / Acetyl-CoA Acetyltransferase 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 ACAT2 / Acetyl-CoA Acetyltransferase captured in each well. The concentration of ACAT2 / Acetyl-CoA Acetyltransferase can then be calculated by reading the O.D. absorbance at 450nm in a microplate reader and referring to the standard curve.