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Spécifications
- Assay duration:Multiple steps
- Assay Type:Sandwich
- Reactivity:Mouse
- Sensitivity:0.234 ng/ml
- Target protein:Caspase-11
- Description:Mouse caspase-11 ELISA kit
- Format:Pre-coated
- Size:96 tests
- Sample type:Serum, plasma, tissue homogenates and other biological fluids
- Cross reactivity:Mouse Caspase-11 ELISA Kit exhibits high specificity and excellent specificity for the detection of mouse Caspase-11. No significant cross-reactivity or interference between Caspase-11 and analogues was observed.
- Detection method:Colorimetric
- Time to Results:4 h 30 min
- Assay Type:Quantitative
- Shelf life:Store for 6 months at 4 °C
- Detection range:0.391 - 25 ng/ml
- Storage temperature:4 °C
- Sample volume:100 μl
- Regulatory status:RUO
Spécifications
A propos de cet article
Mouse Caspase-11 ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of mouse Caspase-11 in serum, plasma, tissue homogenates, and other biological fluids.
- Ready To Use ELISA Kit
- Detection Range: 0.391 to 25 ng/ml
- Sensitivity: 0.234 ng/ml
- Sample Type: Serum, plasma, tissue homogenates, and other biological fluids
- Assay Precision: Intra - Assay: CV <8%, Inter - Assay: CV <10%
Mouse Caspase-11 ELISA Kit (A74697) employs the sandwich enzyme immunoassay technique for the quantitative measurement of mouse Caspase-11 in serum, plasma, tissue homogenates, and other biological fluids. An antibody specific for Caspase-11 has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the Caspase-11 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-Caspase-11 Antibody, which binds the captured Caspase-11 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 Caspase-11 captured in each well. The concentration of Caspase-11 can then be calculated by reading the O.D. absorbance at 450nm in a microplate reader and referring to the standard curve.