Mouse Leukotriene B4 receptor 1/BLT ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of mouse Leukotriene B4 receptor 1/BLT in serum, plasma, tissue homogenates, and other biological fluids.

• Ready To Use ELISA Kit
• Detection Range: 0.313 to 20 ng/ml
• Sensitivity: 0.188 ng/ml
• Sample Type: Serum, plasma, tissue homogenates, and other biological fluids
• Assay Precision: Intra - Assay: CV <8%, Inter - Assay: CV <10%

Mouse Leukotriene B4 Receptor 1 / BLT ELISA Kit (A76907) employs the sandwich enzyme immunoassay technique for the quantitative measurement of mouse Leukotriene B4 Receptor 1 / BLT in serum, plasma, tissue homogenates, and other biological fluids. An antibody specific for Leukotriene B4 Receptor 1 / BLT has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the Leukotriene B4 Receptor 1 / BLT 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-Leukotriene B4 Receptor 1 / BLT Antibody, which binds the captured Leukotriene B4 Receptor 1 / BLT 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 Leukotriene B4 Receptor 1 / BLT captured in each well. The concentration of Leukotriene B4 Receptor 1 / BLT can then be calculated by reading the O.D. absorbance at 450nm in a microplate reader and referring to the standard curve.