Specifications
- Pk:96 Tests
- Assay duration:Multiple steps
- Assay Type:Sandwich
- Format:Pre-coated
- Primary antibody reactivity:Mouse
- Target protein:IL36 alpha/IL-1F6
- Description:Mouse IL36 alpha/IL-1F6 ELISA kit
- Sample type:Serum, plasma, tissue homogenates, and other biological fluids
- Cross reactivity:Mouse IL36 alpha/IL-1F6 ELISA Kit exhibits high specificity and excellent specificity for the detection of mouse IL36 alpha/IL-1F6. No significant cross-reactivity or interference between IL36 alpha/IL-1F6 and analogues was observed.
- Detection method:Colorimetric
- Time to Results:4 h 30 min
- Shelf life:Store for 6 months at 4 °C
- Detection range:15,625 - 1000 pg/ml
- Storage temperature:4 °C
- Sensitivity:9,375 pg/ml
- Regulatory status:RUO
Specifications
About this item
Mouse IL36 alpha/IL-1F6 ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of mouse IL36 alpha/IL-1F6 in serum, plasma, tissue homogenates, and other biological fluids.
- Ready to use ELISA kit
- Assay precision: Intra assay: CV <8%, Inter assay: CV <10%
Mouse IL36 alpha/IL-1F6 ELISA kit (A303602) employs the sandwich enzyme immunoassay technique for the quantitative measurement of mouse IL36 alpha/IL-1F6 in serum, plasma, tissue homogenates, and other biological fluids. An antibody specific for IL36 alpha/IL-1F6 has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the IL36 alpha/IL-1F6 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-IL36 alpha/IL-1F6 Antibody, which binds the captured IL36 alpha/IL-1F6 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 IL36 alpha/IL-1F6 captured in each well. The concentration of IL36 alpha/IL-1F6 can then be calculated by reading the O.D. absorbance at 450 nm in a microplate reader and referring to the standard curve.