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ELK0497-96T, PD1(Protectin D1) ELISA Kit, 96T
3.012,90 RON
PD1(Protectin D1) ELISA Kit
SKU
ELK0497-96T
Alternative Names: Neuroprotectin D1; NPD1
Species: General
Assay Type: Competitive Inhibition
Sensitivity: 0.072 ng/mL
Standard: 10 ng/mL
Detection range: 0.16-10 ng/mL
Sample type: Serum, plasma and other biological fluids.
Assay length: 2.5h
Research Area: Immunology & Inflammation
Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with PD1 protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to PD1. 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 PD1 in the samples is then determined by comparing the OD of the samples to the standard curve.
| Price | 2.490,00 RON (preturile sunt fara TVA) |
|---|---|
| Description |
Alternative Names: Neuroprotectin D1; NPD1 Species: General Assay Type: Competitive Inhibition Sensitivity: 0.072 ng/mL Standard: 10 ng/mL Detection range: 0.16-10 ng/mL Sample type: Serum, plasma and other biological fluids. Assay length: 2.5h Research Area: Immunology & Inflammation Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with PD1 protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to PD1. 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 PD1 in the samples is then determined by comparing the OD of the samples to the standard curve. |
