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- Pk:96 Tests
- Assay duration:Multiple steps
- Assay Type:Sandwich
- Format:Pre-coated
- Primary antibody reactivity:Human
- Target protein:ATP Synthase C
- Description:Human ATP synthase C ELISA kit
- Sample type:Serum, plasma, tissue homogenates and other biological fluids
- Cross reactivity:Human ATP Synthase C ELISA Kit exhibits high specificity and excellent specificity for the detection of human ATP Synthase C. No significant cross-reactivity or interference between ATP Synthase C 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:15,625 - 1000 pg/ml
- Storage temperature:4 °C
- Sample volume:100 μl
- Sensitivity:9,375 pg/ml
- Regulatory status:RUO
Human ATP Synthase C ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human ATP Synthase C in serum, plasma, tissue homogenates, and other biological fluids.
- Ready to use ELISA kit
- Detection range: 15,625 to 1000 pg/ml
- Sensitivity: 9,375 pg/ml
- Sample type: Serum, plasma, tissue homogenates and other biological fluids
- Assay precision: Intra assay: CV <8%, Inter assay: CV <10%
Human ATP Synthase C ELISA kit (A75987) employs the sandwich enzyme immunoassay technique for the quantitative measurement of human ATP Synthase C in serum, plasma, tissue homogenates, and other biological fluids. An antibody specific for ATP Synthase C has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the ATP Synthase C 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-ATP Synthase C Antibody, which binds the captured ATP Synthase C 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 ATP Synthase C captured in each well. The concentration of ATP Synthase C can then be calculated by reading the O.D. absorbance at 450 nm in a microplate reader and referring to the standard curve.