- Assay duration:Multiple steps
- Assay Type (ELISA with LOV):Sandwich
- Format:Pre-coated
- Primary antibody reactivity:Other
- Target protein:Creatine Kinase MB
- Description:Porcine creatine kinase MB ELISA kit
- Size:96 tests
- Sample Type:Serum, plasma, tissue homogenates and other biological fluids
- Cross Reactivity:Porcine Creatine Kinase MB ELISA Kit exhibits high specificity and excellent specificity for the detection of porcine Creatine Kinase MB. No significant cross-reactivity or interference between Creatine Kinase MB 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:0.234 - 15 ng/ml
- Storage Temperature:4 °C
- Sample Volume:100 μl
- Sensitivity:0.141 ng/ml
- Regulatory Status:RUO
- Cat. No.:76745-816
Porcine Creatine Kinase MB ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of porcine Creatine Kinase MB in serum, plasma, tissue homogenates, and other biological fluids.
- Ready To Use ELISA Kit
- Detection Range: 0.234 to 15 ng/ml
- Sensitivity: 0.141 ng/ml
- Sample Type: Serum, plasma, tissue homogenates, and other biological fluids
- Assay Precision: Intra - Assay: CV <8%, Inter - Assay: CV <10%
Porcine Creatine Kinase MB ELISA Kit (A74711) employs the sandwich enzyme immunoassay technique for the quantitative measurement of porcine Creatine Kinase MB in serum, plasma, tissue homogenates, and other biological fluids. An antibody specific for Creatine Kinase MB has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the Creatine Kinase MB 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-Creatine Kinase MB Antibody, which binds the captured Creatine Kinase MB 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 Creatine Kinase MB captured in each well. The concentration of Creatine Kinase MB can then be calculated by reading the O.D. absorbance at 450nm in a microplate reader and referring to the standard curve.