- VE:96 Tests
- Testdauer:Multiple steps
- Testtyp:Sandwich
- Format:Pre-coated
- Reaktivität der primären Antikörper:Rat
- Target protein:ZnT1
- Bezeichnung:Rat ZnT1 ELISA kit
- Probentyp:Serum, plasma, tissue homogenates and other biological fluids
- Kreuzreaktivität:Rat ZnT1 ELISA kit exhibits high specificity and excellent specificity for the detection of rat ZnT1. No significant cross-reactivity or interference between ZnT1 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:78,125 - 5000 pg/ml
- Lagertemperatur:4 °C
- Probenvolumen:100 μl
- Empfindlichkeit:46,875 pg/ml
- Regulatory status:RUO
Rat ZnT1 ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of rat ZnT1 in serum, plasma, tissue homogenates, and other biological fluids.
- Ready to use ELISA kit
- Detection range: 78,125 to 5000 pg/ml
- Sensitivity: 46,875 pg/ml
- Sample type: Serum, plasma, tissue homogenates and other biological fluids
- Assay precision: Intra assay: CV <8%, Inter assay: CV <10%
Rat ZnT1 employs the sandwich enzyme immunoassay technique for the quantitative measurement of rat ZnT1 in serum, plasma, tissue homogenates, and other biological fluids. An antibody specific for ZnT1 has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the ZnT1 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-ZnT1 Antibody, which binds the captured ZnT1 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 ZnT1 captured in each well. The concentration of ZnT1 can then be calculated by reading the O.D. absorbance at 450 nm in a microplate reader and referring to the standard curve.