Specifications
- Assay duration:Multiple steps
- Assay Type (ELISA with LOV):Sandwich
- Format:Pre-coated
- Primary antibody reactivity:Human
- Target protein:Interferon alpha 10
- Description:Human interferon alpha 10 ELISA kit
- Size:96 tests
- Sample Type:Serum, plasma, tissue homogenates and other biological fluids
- Cross Reactivity:Human Interferon alpha 10 ELISA Kit exhibits high specificity and excellent specificity for the detection of human Interferon alpha 10. No significant cross-reactivity or interference between Interferon alpha 10 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 ng/ml
- Storage Temperature:4 °C
- Sample Volume:100 μl
- Sensitivity:9.375 ng/ml
- Regulatory Status:RUO
- Cat. No.:76738-900
Specifications
About this item
Human Interferon alpha 10 ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human Interferon alpha 10 in serum, plasma, tissue homogenates, and other biological fluids.
- Ready To Use ELISA Kit
- Detection Range: 15.625 to 1000 ng/ml
- Sensitivity: 9.375 ng/ml
- Sample Type: Serum, plasma, tissue homogenates, and other biological fluids
- Assay Precision: Intra - Assay: CV <8%, Inter - Assay: CV <10%
Human Interferon alpha 10 ELISA Kit (A75494) employs the sandwich enzyme immunoassay technique for the quantitative measurement of human Interferon alpha 10 in serum, plasma, tissue homogenates, and other biological fluids. An antibody specific for Interferon alpha 10 has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the Interferon alpha 10 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-Interferon alpha 10 Antibody, which binds the captured Interferon alpha 10 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 Interferon alpha 10 captured in each well. The concentration of Interferon alpha 10 can then be calculated by reading the O.D. absorbance at 450nm in a microplate reader and referring to the standard curve.