- Pk:96 T
- Assay duration:Multiple steps
- Assay Type:Competitive
- Format:Pre-coated
- Host:
- Primary antibody reactivity:Rabbit
- Target protein:Prostaglandin F2 alpha
- Description:Rabbit prostaglandin F2 alpha ELISA kit
- Environmentally Preferable:
- Sample type:Serum, plasma, tissue homogenates, and other biological fluids
- Cross reactivity:Rabbit Prostaglandin F2 alpha ELISA Kit exhibits high specificity and excellent specificity for the detection of rabbit Prostaglandin F2 alpha. No significant cross-reactivity or interference between Prostaglandin F2 alpha 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:7,813 - 500 pg/ml
- Storage temperature:4 °C
- Sample volume:50 μl
- Sensitivity:4,688 pg/ml
- Regulatory status:RUO
Rabbit Prostaglandin F2 alpha ELISA kit is a competitive Enzyme-Linked Immunosorbent Assay (cELISA) designed for the in vitro quantitative determination of rabbit Prostaglandin F2 alpha 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 Prostaglandin F2 alpha ELISA kit employs the competitive enzyme immunoassay technique for the quantitative measurement of rabbit Prostaglandin F2 alpha in serum, plasma, tissue homogenates, and other biological fluids. The 96-well microtiter plate has been pre-coated with Prostaglandin F2 alpha antigen. During the incubation, Prostaglandin F2 alpha present in the samples or standards competes with the fixed amount of immobilised Prostaglandin F2 alpha for binding sites on the Biotinylated Anti-Prostaglandin F2 alpha Antibody. The more Prostaglandin F2 alpha present in a sample or standard, the less Biotinylated Anti-Prostaglandin F2 alpha Antibody that binds to the plate. Following incubation, unbound Biotinylated Anti-Prostaglandin F2 alpha 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 Prostaglandin F2 alpha present in each sample or standard. The concentration of Prostaglandin F2 alpha can then be calculated by reading the O.D. absorbance at 450 nm in a microplate reader and referring to the standard curve.