Plant SA (Salicylic Acid) ELISA Kit
Alternative Names: SA
Species: Plant
Assay Type: Competitive Inhibition
Sensitivity: 0.61 ng/mL
Standard: 10 ng/mL
Detection range: 1.57-100 ng/mL
Sample type: plant tissues
Assay length: 2h
Research Area: Enzyme & Kinase;
Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Plant Salicylic Acid protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Plant Salicylic Acid. 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 Plant Salicylic Acid 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: SA Species: Plant Assay Type: Competitive Inhibition Sensitivity: 0.61 ng/mL Standard: 10 ng/mL Detection range: 1.57-100 ng/mL Sample type: plant tissues Assay length: 2h Research Area: Enzyme & Kinase; Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Plant Salicylic Acid protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Plant Salicylic Acid. 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 Plant Salicylic Acid in the samples is then determined by comparing the OD of the samples to the standard curve. |