Specifications
- Assay duration:Multiple steps
- Assay Type:Competitive
- Format:Pre-coated
- Primary antibody reactivity:Rabbit
- Target protein:CRH
- Description:Rabbit CRH ELISA kit
- Sample type:Serum, plasma, tissue homogenates, and other biological fluids
- Cross reactivity:Rabbit CRH ELISA Kit exhibits high specificity and excellent specificity for the detection of rabbit CRH. No significant cross-reactivity or interference between CRH and analogues was observed.
- Detection method:Colorimetric
- Time to Results:2 hours
- Shelf life:Store for 6 months at 4 °C
- Detection range:1,563 - 100 pg/ml
- Storage temperature:4 °C
- Sample volume:50 μl
- Sensitivity:0,938 pg/ml
- Regulatory status:RUO
- Tests per kit:96 tests
Specifications
About this item
Rabbit CRH ELISA Kit is a competitive Enzyme-Linked Immunosorbent Assay (cELISA) designed for the in vitro quantitative determination of rabbit CRH in serum, plasma, tissue homogenates, and other biological fluids.
- Ready-to-use ELISA kit
- Assay Precision: Intra-Assay: CV <8%, Inter-Assay: CV <10%
Rabbit CRH ELISA Kit employs the competitive enzyme immunoassay technique for the quantitative measurement of rabbit CRH in serum, plasma, tissue homogenates, and other biological fluids. The 96-well microtiter plate has been pre-coated with CRH antigen. During the incubation, CRH present in the samples or standards competes with the fixed amount of immobilised CRH for binding sites on the Biotinylated Anti-CRH Antibody. The more CRH present in a sample or standard, the less Biotinylated Anti-CRH Antibody that binds to the plate. Following incubation, unbound Biotinylated Anti-CRH 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 inversely proportional to the amount of CRH present in each sample or standard. The concentration of CRH can then be calculated by reading the O.D. absorbance at 450 nm in a microplate reader and referring to the standard curve.