ELK2934-96T, Human RANk(Receptor Activator Of Nuclear Factor Kappa B) ELISA Kit, 96T

ELK2934-96T, Human RANk(Receptor Activator Of Nuclear Factor Kappa B) ELISA Kit, 96T

ELK2935-96T, Human VLDL(Very Low Density Lipoprotein) ELISA Kit, 96T

ELK2935-96T, Human VLDL(Very Low Density Lipoprotein) ELISA Kit, 96T

ELK2935-48T, Human VLDL(Very Low Density Lipoprotein) ELISA Kit, 48T

2.142,00 RON

Human VLDL(Very Low Density Lipoprotein) ELISA Kit

SKU
ELK2935-48T

Alternative Names: Pre-β-Lipoprotein; Pre-Beta Lipoprotein

Species: Human

Assay Type: Sandwich

Sensitivity: 0.11 ng/mL

Standard: 15 ng/mL

Detection range: 0.24-15 ng/mL

Sample type: serum, plasma and other biological fluids

Assay length: 3.5h

Research Area: Metabolic pathway;Endocrinology;Cardiovascular biology;Nutrition metabolism;

Test principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Human VLDL. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human VLDL. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Human VLDL, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. 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 VLDL in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: Pre-β-Lipoprotein; Pre-Beta Lipoprotein

Species: Human

Assay Type: Sandwich

Sensitivity: 0.11 ng/mL

Standard: 15 ng/mL

Detection range: 0.24-15 ng/mL

Sample type: serum, plasma and other biological fluids

Assay length: 3.5h

Research Area: Metabolic pathway;Endocrinology;Cardiovascular biology;Nutrition metabolism;

Test principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Human VLDL. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human VLDL. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Human VLDL, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. 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 VLDL in the samples is then determined by comparing the OD of the samples to the standard curve.