Specifications
- Cdt:96 Tests
- Durée du test:Multiple steps
- Type de test:Sandwich
- Format:Pre-coated
- Hôte:
- Primary antibody reactivity:Rat
- Cible:Alanine Transaminase 1
- Désignation:Rat alanine transaminase 1 ELISA kit
- Environmentally Preferable:
- Type déchantillon:Serum, plasma, tissue homogenates and other biological fluids
- Réactivité croisée:Rat Alanine Transaminase 1 ELISA Kit exhibits high specificity and excellent specificity for the detection of rat Alanine Transaminase 1. No significant cross-reactivity or interference between Alanine Transaminase 1 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:0,313 - 20 mIU/ml
- Température de stockage:4 °C
- Volume d'échantillon:100 μl
- Sensibilité:0,188 mIU/ml
- Regulatory status:RUO
Specifications
About this item
Rat Alanine Transaminase 1 ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of rat Alanine Transaminase 1 in serum, plasma, tissue homogenates, and other biological fluids.
- Ready to use ELISA kit
- Detection range: 0,313 to 20 mIU/ml
- Sensitivity: 0,188 mIU/ml
- Sample type: Serum, plasma, tissue homogenates and other biological fluids
- Assay precision: Intra - Assay: CV <8%, Inter - Assay: CV <10%
Rat Alanine Transaminase 1 ELISA kit employs the sandwich enzyme immunoassay technique for the quantitative measurement of rat Alanine Transaminase 1 in serum, plasma, tissue homogenates, and other biological fluids. An antibody specific for Alanine Transaminase 1 has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the Alanine Transaminase 1 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-Alanine Transaminase 1 Antibody, which binds the captured Alanine Transaminase 1 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 Alanine Transaminase 1 captured in each well. The concentration of Alanine Transaminase 1 can then be calculated by reading the O.D. absorbance at 450 nm in a microplate reader and referring to the standard curve.