Spécifications
- Durée du test:Multiple steps
- Type de test:Sandwich
- Format:Pre-coated
- Primary antibody reactivity:Human
- Cible:beta Crosslaps/beta CTx
- Désignation:Human beta Crosslaps/beta CTx ELISA kit
- Type déchantillon:Serum, plasma, tissue homogenates, and other biological fluids
- Réactivité croisée:Human beta Crosslaps/beta CTx ELISA Kit exhibits high specificity and excellent specificity for the detection of human beta Crosslaps/beta CTx. No significant cross-reactivity or interference between beta Crosslaps/beta CTx and analogues was observed.
- Méthode de détection:Colorimetric
- Time to Results:4 hours
- Durée de conservation:Store for 6 months at 4 °C
- Portée de détection:7,813 - 500 pg/ml
- Température de stockage:4 °C
- Volume d'échantillon:100 μl
- Sensibilité:4,688 pg/ml
- Regulatory status:RUO
- Tests par set:96 tests
Spécifications
À propos de cet article
Human beta Crosslaps/beta CTx ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human beta Crosslaps/beta CTx in serum, plasma, tissue homogenates, and other biological fluids.
- Ready-To-Use ELISA kit
- Assay Precision: Intra-Assay: CV <8%, Inter-Assay: CV <10%
Human beta Crosslaps/beta CTx ELISA kit employs the sandwich enzyme immunoassay technique for the quantitative measurement of human beta Crosslaps/beta CTx in serum, plasma, tissue homogenates, and other biological fluids. An antibody specific for beta Crosslaps/beta CTx has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the beta Crosslaps/beta CTx 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-beta Crosslaps/beta CTx Antibody, which binds the captured beta Crosslaps/beta CTx 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 beta Crosslaps/beta CTx captured in each well. The concentration of beta Crosslaps/beta CTx can then be calculated by reading the O.D. absorbance at 450 nm in a microplate reader and referring to the standard curve.