ELK1811-48T, Human CA50(Carbohydrate Antigen 50) ELISA Kit, 48T

ELK1811-48T, Human CA50(Carbohydrate Antigen 50) ELISA Kit, 48T

ELK1812-48T, Human SNCa(Synuclein Alpha) ELISA Kit, 48T

ELK1812-48T, Human SNCa(Synuclein Alpha) ELISA Kit, 48T

ELK1811-96T, Human CA50(Carbohydrate Antigen 50) ELISA Kit, 96T

2.963,10 RON

Human CA50(Carbohydrate Antigen 50) ELISA Kit

SKU
ELK1811-96T

Alternative Names: cancer Antigen 50

Species: Human

Assay Type: Sandwich

Sensitivity: 1.29 ng/mL

Standard: 200 ng/mL

Detection range: 3.13-200 ng/mL

Sample type: Serum, plasma and other biological fluids

Assay length: 3.5h

Research Area: Tumor immunity;Gastroenterology;

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 CA50. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human CA50. 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 CA50, 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 CA50 in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: cancer Antigen 50

Species: Human

Assay Type: Sandwich

Sensitivity: 1.29 ng/mL

Standard: 200 ng/mL

Detection range: 3.13-200 ng/mL

Sample type: Serum, plasma and other biological fluids

Assay length: 3.5h

Research Area: Tumor immunity;Gastroenterology;

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 CA50. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human CA50. 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 CA50, 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 CA50 in the samples is then determined by comparing the OD of the samples to the standard curve.