TXB2(Thromboxane B2) ELISA Kit
Alternative Names: TX-B2
Species: General
Assay Type: Competitive Inhibition
Sensitivity: 7.2 pg/mL
Standard: 1500 pg/mL
Detection range: 23.44-1500 pg/mL
Sample type: Serum, plasma and other biological fluids
Assay length: 2h
Research Area: Metabolic pathway;Infection immunity;
Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with TXB2 protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to TXB2. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of TXB2 in the samples is then determined by comparing the OD of the samples to the standard curve.
Price | 2.080,00 RON (preturile sunt fara TVA) |
---|---|
Description |
Alternative Names: TX-B2 Species: General Assay Type: Competitive Inhibition Sensitivity: 7.2 pg/mL Standard: 1500 pg/mL Detection range: 23.44-1500 pg/mL Sample type: Serum, plasma and other biological fluids Assay length: 2h Research Area: Metabolic pathway;Infection immunity; Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with TXB2 protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to TXB2. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of TXB2 in the samples is then determined by comparing the OD of the samples to the standard curve. |