Spécifications
- Cdt:96 Tests
- Durée du test:One step
- Type de test:Sandwich
- Format:Pre-coated
- Hôte:
- Primary antibody reactivity:Human
- Cible:IRK-2
- Désignation:Human IRK-2 ELISA kit
- Environmentally Preferable:
- Type déchantillon:Serum, plasma or other biological fluids
- Méthode de détection:Colorimetric
- Time to Results:1 h 30 min
- Durée de conservation:Store for 6 months at 4 °C
- Portée de détection:0,75 - 12 ng/ml
- Température de stockage:4 °C
- Volume d'échantillon:40 μl
- Sensibilité:0,021 ng/ml
- Regulatory status:RUO
Spécifications
À propos de cet article
Human IRK-2 ELISA kit is a 90 minutes sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human IRK-2 in serum, plasma, and other biological fluids.
- Higher throughput: Get results in just 90 minutess, with a single wash step
- Detection Range: 0,75 to 12 ng/ml
- Sensitivity: 0,021 ng/ml
- Sample Type: Serum, plasma or other biological fluids
- Assay Precision: Intra-Assay: CV <8%, Inter-Assay: CV <10%
Human IRK-2 ELISA kit employs the sandwich enzyme immunoassay technique for the quantitative measurement of human IRK-2 in serum, plasma or other biological fluids. An antibody specific for IRK-2 has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the IRK-2 present in each sample is bound to the wells by the immobilised antibody. Biotinylated anti-IRK-2 antibody, which also binds the IRK-2 present in each sample, and Streptavidin-HRP, which binds the Biotinylated anti-IRK-2 antibody, are added and the microtiter plate is incubated. Following incubation, unbound Biotinylated anti-IRK-2 antibody and unbound Streptavidin-HRP are removed by washing, and two substrate solutions are added to the wells. colour develops in proportion to the amount of IRK-2 captured in each well. The colour development is stopped by addition of stop solution which changes the colour from blue to yellow and the intensity of the colour is then measured. The concentration of IRK-2 in the samples can then be calculated by reading the O.D. absorbance at 450 nm in a microplate reader and referring to the standard curve.