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- Pk:96 Tests
- Assay duration:Multiple steps
- Assay Type:Competitive
- Format:Pre-coated
- Host:
- Primary antibody reactivity:Mouse
- Target protein:Free Thyroxine/T4
- Description:Mouse free thyroxine/T4 ELISA kit
- Environmentally Preferable:
- Sample type:Serum, plasma, tissue homogenates and other biological fluids
- Cross reactivity:Mouse Free Thyroxine/T4 ELISA kit exhibits high specificity and excellent specificity for the detection of mouse Free Thyroxine/T4. No significant cross-reactivity or interference between Free Thyroxine/T4 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:1,563 - 100 pg/ml
- Storage temperature:4 °C
- Sample volume:50 μl
- Sensitivity:0,938 pg/ml
- Regulatory status:RUO
Mouse Free Thyroxine/T4 ELISA kit is a competitive Enzyme-Linked Immunosorbent Assay (cELISA) designed for the in vitro quantitative determination of mouse Free Thyroxine/T4 in serum, plasma, tissue homogenates, and other biological fluids.
- Ready to use ELISA kit
- Detection range: 1,563 to 100 pg/ml
- Sensitivity: 0,938 pg/ml
- Sample type: Serum, plasma, tissue homogenates, and other biological fluids
- Assay Precision: Intra assay: CV <8%, Inter assay: CV <10%
Mouse Free Thyroxine/T4 ELISA kit (A78110) employs the competitive enzyme immunoassay technique for the quantitative measurement of mouse Free Thyroxine/T4 in serum, plasma, tissue homogenates, and other biological fluids. The 96-well microtiter plate has been pre-coated with Free Thyroxine/T4 antigen. During the incubation, Free Thyroxine/T4 present in the samples or standards competes with the fixed amount of immobilised Free Thyroxine/T4 for binding sites on the Biotinylated Anti-Free Thyroxine/T4 Antibody. The more Free Thyroxine/T4 present in a sample or standard, the less Biotinylated Anti-Free Thyroxine/T4 Antibody that binds to the plate. Following incubation, unbound Biotinylated Anti-Free Thyroxine/T4 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 Free Thyroxine/T4 present in each sample or standard. The concentration of Free Thyroxine/T4 can then be calculated by reading the O.D. absorbance at 450 nm in a microplate reader and referring to the standard curve.