Rabbit FPA(Fibrinopeptide A) ELISA Kit
Alternative Names: FP-A
Species: Rabbit
Assay Type: Competitive Inhibition
Sensitivity: 136.7 pg/mL
Standard: 30000 pg/mL
Detection range: 468.75-30000 pg/mL
Sample type: Plasma.
Assay length: 2h
Research Area: Signal transduction;Hematology;
Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Rabbit FPA protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rabbit FPA. 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 Rabbit FPA in the samples is then determined by comparing the OD of the samples to the standard curve.
Price | 1.800,00 RON (preturile sunt fara TVA) |
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Description |
Alternative Names: FP-A Species: Rabbit Assay Type: Competitive Inhibition Sensitivity: 136.7 pg/mL Standard: 30000 pg/mL Detection range: 468.75-30000 pg/mL Sample type: Plasma. Assay length: 2h Research Area: Signal transduction;Hematology; Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Rabbit FPA protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rabbit FPA. 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 Rabbit FPA in the samples is then determined by comparing the OD of the samples to the standard curve. |