- Assay duration:Multiple steps
- Assay Type (ELISA with LOV):Sandwich
- Format:Pre-coated
- Primary antibody reactivity:Mouse
- Target protein:Pancreatic alpha Amylase
- Description:Mouse pancreatic alpha amylase ELISA kit
- Size:96 tests
- Sample Type:Serum, plasma, tissue homogenates and other biological fluids
- Cross Reactivity:Mouse Pancreatic alpha Amylase ELISA Kit exhibits high specificity and excellent specificity for the detection of mouse Pancreatic alpha Amylase. No significant cross-reactivity or interference between Pancreatic alpha Amylase and analogues was observed.
- Detection Method:Colorimetric
- Time to Results:4 h 30 min
- Assay Principle:Quantitative
- Shelf Life:Store for 6 months at 4 °C
- Detection Range:1.563 - 100 mIU/ml
- Storage Temperature:4 °C
- Sample Volume:100 μl
- Sensitivity:0.938 mIU/ml
- Regulatory Status:RUO
- Cat. No.:76735-108
Mouse Pancreatic alpha Amylase ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of mouse Pancreatic alpha Amylase in serum, plasma, tissue homogenates, and other biological fluids.
- Ready to use ELISA kit
- Detection range: 1.563 to 100 mIU/ml
- Sensitivity: 0.938 mIU/ml
- Sample type: Serum, plasma, tissue homogenates and other biological fluids
- Assay precision: Intra assay: CV <8%, Inter assay: CV <10%
Mouse Pancreatic alpha Amylase ELISA kit (A77678) employs the sandwich enzyme immunoassay technique for the quantitative measurement of mouse Pancreatic alpha Amylase in serum, plasma, tissue homogenates, and other biological fluids. An antibody specific for Pancreatic alpha Amylase has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the Pancreatic alpha Amylase 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-Pancreatic alpha Amylase Antibody, which binds the captured Pancreatic alpha Amylase 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 Pancreatic alpha Amylase captured in each well. The concentration of Pancreatic alpha Amylase can then be calculated by reading the O.D. absorbance at 450 nm in a microplate reader and referring to the standard curve.