- Cdt:96 Tests
- Durée du test:Multiple steps
- Type de test:Sandwich
- Format:Pre-coated
- Primary antibody reactivity:Mouse
- Cible:Retinoic Acid receptor beta
- Désignation:Mouse Retinoic Acid receptor beta ELISA kit
- Type déchantillon:Serum, plasma, tissue homogenates and other biological fluids
- Réactivité croisée:Mouse Retinoic Acid receptor beta ELISA kit exhibits high specificity and excellent specificity for the detection of mouse Retinoic Acid receptor beta. No significant cross-reactivity or interference between Retinoic Acid receptor beta and analogues was observed.
- Méthode de détection:Colorimetric
- Time to Results:4 h 30 min
- Principe du test:Quantitative
- Durée de conservation:Store for 6 months at 4 °C
- Portée de détection:46,875 - 3000 pg/ml
- Température de stockage:4 °C
- Volume d'échantillon:100 μl
- Sensibilité:28,125 pg/ml
- Regulatory status:RUO
Mouse Retinoic Acid receptor beta ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of mouse Retinoic Acid receptor beta in serum, plasma, tissue homogenates, and other biological fluids.
- Ready to use ELISA kit
- Detection range: 46,875 to 3000 pg/ml
- Sensitivity: 28,125 pg/ml
- Sample type: Serum, plasma, tissue homogenates, and other biological fluids
- Assay Precision: Intra assay: CV <8%, Inter assay: CV <10%
Mouse Retinoic Acid Receptor beta ELISA kit (A78716) employs the sandwich enzyme immunoassay technique for the quantitative measurement of mouse Retinoic Acid Receptor beta in serum, plasma, tissue homogenates, and other biological fluids. An antibody specific for Retinoic Acid Receptor beta has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the Retinoic Acid Receptor beta present in each sample is bound to the wells by the immobilised antibody. Following incubation, the wells are washed and then incubated with Biotinylated Anti-Retinoic Acid Receptor beta Antibody, which binds the captured Retinoic Acid Receptor beta present in each well. Following incubation, unbound biotinylated detection 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 proportional to the amount of Retinoic Acid Receptor beta captured in each well. The concentration of Retinoic Acid Receptor beta can then be calculated by reading the O.D. absorbance at 450 nm in a microplate reader and referring to the standard curve.