Mouse Glycosylated Hemoglobin A1c ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of mouse Glycosylated Hemoglobin A1c in serum, plasma, tissue homogenates, and other biological fluids.

• Ready to use ELISA kit
• Detection range: 1,25 to 80 ng/ml
• Sensitivity: 0,75 ng/ml
• Sample type: Serum, plasma, tissue homogenates, and other biological fluids
• Assay precision: Intra assay: CV <8%, Inter assay: CV <10%

Mouse Glycosylated Hemoglobin A1c employs the sandwich enzyme immunoassay technique for the quantitative measurement of mouse Glycosylated Hemoglobin A1c in serum, plasma, tissue homogenates, and other biological fluids. An antibody specific for Glycosylated Hemoglobin A1c has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the Glycosylated Hemoglobin A1c present in each sample is bound to the wells by the immobilised antibody. Following incubation, the wells are washed and then incubated with Biotinylated Anti-Glycosylated Hemoglobin A1c Antibody, which binds the captured Glycosylated Hemoglobin A1c 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 visualise 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 Glycosylated Hemoglobin A1c captured in each well. The concentration of Glycosylated Hemoglobin A1c can then be calculated by reading the O.D. absorbance at 450 nm in a microplate reader and referring to the standard curve.