- Pk:96 Tests
- Assay duration:Multiple steps
- Assay Type:Competitive
- Format:Pre-coated
- Primary antibody reactivity:Mouse
- Target protein:Testosterone
- Description:Mouse testosterone ELISA kit
- Sample type:Serum, plasma, tissue homogenates and other biological fluids
- Cross reactivity:Mouse Testosterone ELISA kit exhibits high specificity and excellent specificity for the detection of mouse Testosterone. No significant cross-reactivity or interference between Testosterone and analogues was observed.
- Detection method:Colorimetric
- Time to Results:4 h 30 min
- Assay Principle:Quantitative
- Shelf life:Store for 6 months at 4 °C
- Detection range:0,313 - 20 ng/ml
- Storage temperature:4 °C
- Sample volume:50 μl
- Sensitivity:0,188 ng/ml
- Regulatory status:RUO
Mouse Testosterone ELISA kit is a competitive Enzyme-Linked Immunosorbent Assay (cELISA) designed for the in vitro quantitative determination of mouse Testosterone in serum, plasma, tissue homogenates, and other biological fluids.
- Ready-to-use ELISA kit
- Detection Range: 0,313 to 20 ng/ml
- Sensitivity: 0,188 ng/ml
- Sample Type: Serum, plasma, tissue homogenates, and other biological fluids
- Assay Precision: Intra-Assay: CV <8%, Inter-Assay: CV <10%
Mouse Testosterone ELISA kit employs the competitive enzyme immunoassay technique for the quantitative measurement of mouse Testosterone in serum, plasma, tissue homogenates, and other biological fluids. The 96-well microtiter plate has been pre-coated with Testosterone antigen. During the incubation, Testosterone present in the samples or standards competes with the fixed amount of immobilised Testosterone for binding sites on the Biotinylated Anti-Testosterone Antibody. The more Testosterone present in a sample or standard, the less Biotinylated Anti-Testosterone Antibody that binds to the plate. Following incubation, unbound Biotinylated Anti-Testosterone 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 Testosterone present in each sample or standard. The concentration of Testosterone can then be calculated by reading the O.D. absorbance at 450 nm in a microplate reader and referring to the standard curve.