Specifications
- Pk:96 Tests
- Assay duration:Multiple steps
- Assay Type:Sandwich
- Format:Pre-coated
- Primary antibody reactivity:Mouse
- Target protein:Apolipoprotein CI/Apo-CI
- Description:Mouse apolipoprotein CI/Apo-CI ELISA kit
- Sample type:Serum, plasma, tissue homogenates and other biological fluids
- Cross reactivity:Mouse Apolipoprotein CI/Apo-CI ELISA kit exhibits high specificity and excellent specificity for the detection of mouse Apolipoprotein CI/Apo-CI. No significant cross-reactivity or interference between Apolipoprotein CI/Apo-CI 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:62,5 - 4000 ng/ml
- Storage temperature:4 °C
- Sample volume:100 μl
- Sensitivity:37,5 ng/ml
- Regulatory status:RUO
Specifications
About this item
Mouse Apolipoprotein CI/Apo-CI ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of mouse Apolipoprotein CI/Apo-CI in serum, plasma, tissue homogenates, and other biological fluids.
- Ready-to-use ELISA kit
- Detection range: 62,5 to 4000 ng/ml
- Sensitivity: 37,5 ng/ml
- Sample type: Serum, plasma, tissue homogenates, and other biological fluids
- Assay Precision: Intra-Assay: CV <8%, Inter-Assay: CV <10%
Mouse Apolipoprotein CI/Apo-CI ELISA kit (A74663) employs the sandwich enzyme immunoassay technique for the quantitative measurement of mouse Apolipoprotein CI/Apo-CI in serum, plasma, tissue homogenates, and other biological fluids. An antibody specific for Apolipoprotein CI/Apo-CI has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the Apolipoprotein CI/Apo-CI 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-Apolipoprotein CI/Apo-CI Antibody, which binds the captured Apolipoprotein CI/Apo-CI 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 Apolipoprotein CI/Apo-CI captured in each well. The concentration of Apolipoprotein CI/Apo-CI can then be calculated by reading the O.D. absorbance at 450 nm in a microplate reader and referring to the standard curve.