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ELK8169-48T, TG(Triglyceride) ELISA Kit, 48T
1.814,75 RON
TG(Triglyceride) ELISA Kit
SKU
ELK8169-48T
Alternative Names: TAG; Triacylglycerol; Triacylglyceride
Species: General
Assay Type: Competitive Inhibition
Sensitivity: 1.8 µg/mL
Standard: 1000 µg/mL
Detection range: 15.63-1000 µg/mL
Sample type: serum, plasma, tissue homogenates and other biological fluids
Assay length: 2h
Research Area: Metabolic pathway;Cardiovascular biology;Hepatology;Nutrition metabolism;
Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with TG protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to TG. 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 TG in the samples is then determined by comparing the OD of the samples to the standard curve.
| Price | 1.525,00 RON (preturile sunt fara TVA) |
|---|---|
| Description |
Alternative Names: TAG; Triacylglycerol; Triacylglyceride Species: General Assay Type: Competitive Inhibition Sensitivity: 1.8 µg/mL Standard: 1000 µg/mL Detection range: 15.63-1000 µg/mL Sample type: serum, plasma, tissue homogenates and other biological fluids Assay length: 2h Research Area: Metabolic pathway;Cardiovascular biology;Hepatology;Nutrition metabolism; Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with TG protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to TG. 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 TG in the samples is then determined by comparing the OD of the samples to the standard curve. |
