Specifications
- Pk:96 Tests
- Assay duration:Multiple steps
- Assay Type:Sandwich
- Format:Pre-coated
- Host:
- Primary antibody reactivity:Mouse
- Target protein:MMP2
- Description:Mouse MMP2 ELISA kit
- Environmentally Preferable:
- Sample type:Serum, plasma, tissue homogenates and other biological fluids
- Cross reactivity:Mouse MMP2 ELISA kit exhibits high specificity and excellent specificity for the detection of mouse MMP2. No significant cross-reactivity or interference between MMP2 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:0,313 - 20 ng/ml
- Storage temperature:4 °C
- Sample volume:100 μl
- Sensitivity:0,188 ng/ml
- Regulatory status:RUO
Specifications
About this item
Mouse MMP2 ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of mouse MMP2 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 MMP2 employs the sandwich enzyme immunoassay technique for the quantitative measurement of mouse MMP2 in serum, plasma, tissue homogenates, and other biological fluids. An antibody specific for MMP2 has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the MMP2 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-MMP2 Antibody, which binds the captured MMP2 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 MMP2 captured in each well. The concentration of MMP2 can then be calculated by reading the O.D. absorbance at 450 nm in a microplate reader and referring to the standard curve.