Specifications
- VE:96 Tests
- Testdauer:Multiple steps
- Testtyp:Sandwich
- Format:Pre-coated
- Reaktivität der primären Antikörper:Human
- Target protein:SLC16A8
- Bezeichnung:Human SLC16A8 ELISA kit
- Probentyp:Serum, plasma, tissue homogenates and other biological fluids
- Kreuzreaktivität:Human SLC16A8 ELISA kit exhibits high specificity and excellent specificity for the detection of human SLC16A8. No significant cross-reactivity or interference between SLC16A8 and analogues was observed.
- Erkennungsmethode:Colorimetric
- Time to Results:4 h 30 min
- Testprinzip:Quantitative
- Shelf life:Store for 6 months at 4 °C
- Erfassungsbereich:0,625 - 40 ng/ml
- Lagertemperatur:4 °C
- Probenvolumen:100 μl
- Empfindlichkeit:0,375 ng/ml
- Regulatory status:RUO
Specifications
About this item
Human SLC16A8 ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human SLC16A8 in serum, plasma, tissue homogenates, and other biological fluids.
- Ready-to-use ELISA kit
- Detection range: 0,625 to 40 ng/ml
- Sensitivity: 0,375 ng/ml
- Sample type: Serum, plasma, tissue homogenates, and other biological fluids
- Assay Precision: Intra-Assay: CV <8%, Inter-Assay: CV <10%
Human SLC16A8 ELISA kit (A74997) employs the sandwich enzyme immunoassay technique for the quantitative measurement of human SLC16A8 in serum, plasma, tissue homogenates, and other biological fluids. An antibody specific for SLC16A8 has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the SLC16A8 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-SLC16A8 Antibody, which binds the captured SLC16A8 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 SLC16A8 captured in each well. The concentration of SLC16A8 can then be calculated by reading the O.D. absorbance at 450 nm in a microplate reader and referring to the standard curve.