Specifications
- Pk:96 Tests
- Assay duration:Multiple steps
- Assay Type:Sandwich
- Format:Pre-coated
- Primary antibody reactivity:Chicken
- Target protein:KIR3DL1
- Description:Chicken KIR3DL1 ELISA kit
- Sample type:Serum, plasma, tissue homogenates, and other biological fluids
- Cross reactivity:Chicken KIR3DL1 ELISA Kit exhibits high specificity and excellent specificity for the detection of chicken KIR3DL1. No significant cross-reactivity or interference between KIR3DL1 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:0,156 - 10 ng/ml
- Storage temperature:4 °C
- Sensitivity:0,094 ng/ml
- Regulatory status:RUO
Specifications
About this item
Chicken KIR3DL1 ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of chicken KIR3DL1 in serum, plasma, tissue homogenates, and other biological fluids.
- Ready to use ELISA kit
- Assay precision: Intra assay: CV <8%, Inter assay: CV <10%
Chicken KIR3DL1 ELISA kit (A303349) employs the sandwich enzyme immunoassay technique for the quantitative measurement of chicken KIR3DL1 in serum, plasma, tissue homogenates, and other biological fluids. An antibody specific for KIR3DL1 has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the KIR3DL1 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-KIR3DL1 Antibody, which binds the captured KIR3DL1 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 KIR3DL1 captured in each well. The concentration of KIR3DL1 can then be calculated by reading the O.D. absorbance at 450 nm in a microplate reader and referring to the standard curve.