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ELK8535-96T, MGO(Methylglyoxal) ELISA Kit, 96T
2.475,20 RON
MGO(Methylglyoxal) ELISA Kit
SKU
ELK8535-96T
Alternative Names: Methylglyoxal
Species: General
Assay Type: Competitive Inhibition
Sensitivity: 0.51 ng/mL
Standard: 100 ng/mL
Detection range: 1.57-100 ng/mL
Sample type: serum, plasma and other biological fluids
Assay length: 2h
Research Area: Signal transduction;Metabolic pathway;
Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with MGO protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to MGO. 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 MGO 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: Methylglyoxal Species: General Assay Type: Competitive Inhibition Sensitivity: 0.51 ng/mL Standard: 100 ng/mL Detection range: 1.57-100 ng/mL Sample type: serum, plasma and other biological fluids Assay length: 2h Research Area: Signal transduction;Metabolic pathway; Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with MGO protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to MGO. 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 MGO in the samples is then determined by comparing the OD of the samples to the standard curve. |
