Spécifications
- Durée du test:Multiple steps
- Type de test:Sandwich
- Format:Pre-coated
- Primary antibody reactivity:Goat
- Cible:VEGFA
- Désignation:Goat VEGFA ELISA kit
- Type déchantillon:Serum, plasma, tissue homogenates, and other biological fluids
- Réactivité croisée:Goat VEGFA ELISA Kit exhibits high specificity and excellent specificity for the detection of goat VEGFA. No significant cross-reactivity or interference between VEGFA 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:31,25 - 2000 pg/ml
- Température de stockage:4 °C
- Volume d'échantillon:100 μl
- Sensibilité:18,75 pg/ml
- Regulatory status:RUO
- Tests par set:96 tests
Spécifications
À propos de cet article
Goat VEGFA ELISA Kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of goat VEGFA in serum, plasma, tissue homogenates, and other biological fluids.
- Ready-to-use ELISA kit
- Assay Precision: Intra-Assay: CV <8%, Inter-Assay: CV <10%
Goat VEGFA ELISA Kit employs the sandwich enzyme immunoassay technique for the quantitative measurement of goat VEGFA in serum, plasma, tissue homogenates, and other biological fluids. An antibody specific for VEGFA has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the VEGFA 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-VEGFA Antibody, which binds the captured VEGFA 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 VEGFA captured in each well. The concentration of VEGFA can then be calculated by reading the O.D. absorbance at 450 nm in a microplate reader and referring to the standard curve.