ELK7869-96T, HA(Histamine) ELISA Kit, 96T

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ELK7870-96T, VD2(Vitamin D2) ELISA Kit, 96T

ELK7870-96T, VD2(Vitamin D2) ELISA Kit, 96T

ELK7870-48T, VD2(Vitamin D2) ELISA Kit, 48T

1.814,75 RON

VD2(Vitamin D2) ELISA Kit

SKU
ELK7870-48T

Alternative Names: Ergocalciferol; Deltalin; Drisdol; Calcidol

Species: General

Assay Type: Competitive Inhibition

Sensitivity: 0.53 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: Metabolic pathway;Neuro science;Nutrition metabolism;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 VD2 protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to VD2. 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 VD2 in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: Ergocalciferol; Deltalin; Drisdol; Calcidol

Species: General

Assay Type: Competitive Inhibition

Sensitivity: 0.53 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: Metabolic pathway;Neuro science;Nutrition metabolism;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 VD2 protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to VD2. 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 VD2 in the samples is then determined by comparing the OD of the samples to the standard curve.