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ELK0370-96T, Chicken VLDL(Very Low Density Lipoprotein) ELISA Kit, 96T

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ELK0370-48T, Chicken VLDL(Very Low Density Lipoprotein) ELISA Kit, 48T

2.142,00 RON

Chicken VLDL(Very Low Density Lipoprotein) ELISA Kit

SKU
ELK0370-48T

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

Species: Chicken

Assay Type: Sandwich

Sensitivity: 0.23 ng/mL

Standard: 50 ng/mL

Detection range: 0.78-50 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 Chicken VLDL. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Chicken 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 Chicken 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 Chicken 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: Chicken

Assay Type: Sandwich

Sensitivity: 0.23 ng/mL

Standard: 50 ng/mL

Detection range: 0.78-50 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 Chicken VLDL. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Chicken 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 Chicken 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 Chicken VLDL in the samples is then determined by comparing the OD of the samples to the standard curve.