Specifications
- Assay duration:Multiple steps
- Assay Type:Competitive
- Format:Pre-coated
- Primary antibody reactivity:Rabbit
- Target protein:FSH
- Description:Rabbit FSH ELISA kit
- Sample type:Serum, plasma, tissue homogenates, and other biological fluids
- Cross reactivity:Rabbit FSH ELISA Kit exhibits high specificity and excellent specificity for the detection of rabbit FSH. No significant cross-reactivity or interference between FSH 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 mIU/ml
- Storage temperature:4 °C
- Sample volume:50 μl
- Sensitivity:0,938m IU/ml
- Regulatory status:RUO
- Tests per kit:96 tests
Specifications
About this item
Rabbit FSH ELISA kit is a competitive Enzyme-Linked Immunosorbent Assay (cELISA) designed for the in vitro quantitative determination of rabbit FSH 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 FSH ELISA kit employs the competitive enzyme immunoassay technique for the quantitative measurement of rabbit FSH in serum, plasma, tissue homogenates, and other biological fluids. The 96-well microtiter plate has been pre-coated with FSH antigen. During the incubation, FSH present in the samples or standards competes with the fixed amount of immobilised FSH for binding sites on the Biotinylated Anti-FSH Antibody. The more FSH present in a sample or standard, the less Biotinylated Anti-FSH Antibody that binds to the plate. Following incubation, unbound Biotinylated Anti-FSH 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 FSH present in each sample or standard. The concentration of FSH can then be calculated by reading the O.D. absorbance at 450 nm in a microplate reader and referring to the standard curve.