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ELK9785-48T, Human SDMA(Symmetric dimethylarginine) ELISA Kit, 48T
2.142,00 RON
Human SDMA(Symmetric dimethylarginine) ELISA Kit
SKU
ELK9785-48T
Alternative Names: Symmetric dimethylarginine
Species: Human
Assay Type: Competitive Inhibition
Sensitivity: 0.119 nmol/mL
Standard: 20 nmol/mL
Detection range: 0.32-20 nmol/mL
Sample type: EDTA Plasma, Serum
Assay length: 2h
Research Area: Signal transduction;Developmental science;Bone metabolism;
Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Human SDMA protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human SDMA. 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 Human SDMA 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) |
|---|---|
| Description |
Alternative Names: Symmetric dimethylarginine Species: Human Assay Type: Competitive Inhibition Sensitivity: 0.119 nmol/mL Standard: 20 nmol/mL Detection range: 0.32-20 nmol/mL Sample type: EDTA Plasma, Serum Assay length: 2h Research Area: Signal transduction;Developmental science;Bone metabolism; Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Human SDMA protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human SDMA. 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 Human SDMA in the samples is then determined by comparing the OD of the samples to the standard curve. |
