Spécifications
- Cdt:96 Tests
- Durée du test:Multiple steps
- Type de test:Sandwich
- Format:Pre-coated
- Hôte:
- Primary antibody reactivity:Rat
- Cible:Adenosine Receptor A2a
- Désignation:Rat adenosine receptor A2a ELISA kit
- Environmentally Preferable:
- Type déchantillon:Serum, plasma, tissue homogenates and other biological fluids
- Réactivité croisée:Rat Adenosine Receptor A2a ELISA kit exhibits high specificity and excellent specificity for the detection of rat Adenosine Receptor A2a. No significant cross-reactivity or interference between Adenosine Receptor A2a 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:0,156 - 10 ng/ml
- Température de stockage:4 °C
- Volume d'échantillon:100 μl
- Sensibilité:0,094 ng/ml
- Regulatory status:RUO
Spécifications
À propos de cet article
Rat Adenosine Receptor A2a ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of rat Adenosine Receptor A2a in serum, plasma, tissue homogenates, and other biological fluids.
- Ready to use ELISA kit
- Detection range: 0,156 to 10 ng/ml
- Sensitivity: 0,094 ng/ml
- Sample type: Serum, plasma, tissue homogenates, and other biological fluids
- Assay precision: Intra assay: CV <8%, Inter assay: CV <10%
Rat Adenosine Receptor A2a ELISA kit (A76108) employs the sandwich enzyme immunoassay technique for the quantitative measurement of rat Adenosine Receptor A2a in serum, plasma, tissue homogenates, and other biological fluids. An antibody specific for Adenosine Receptor A2a has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the Adenosine Receptor A2a 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-Adenosine Receptor A2a Antibody, which binds the captured Adenosine Receptor A2a 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 Adenosine Receptor A2a captured in each well. The concentration of Adenosine Receptor A2a can then be calculated by reading the O.D. absorbance at 450 nm in a microplate reader and referring to the standard curve.