ELK7351-96T, Mouse PRM2(Protamine 2) ELISA Kit, 96T

ELK7351-96T, Mouse PRM2(Protamine 2) ELISA Kit, 96T

ELK7352-96T, Human bMSH(Beta-Melanocyte Stimulating Hormone) ELISA Kit, 96T

ELK7352-96T, Human bMSH(Beta-Melanocyte Stimulating Hormone) ELISA Kit, 96T

ELK7352-48T, Human bMSH(Beta-Melanocyte Stimulating Hormone) ELISA Kit, 48T

2.142,00 RON

Human bMSH(Beta-Melanocyte Stimulating Hormone) ELISA Kit

SKU
ELK7352-48T

Alternative Names: β-MSH

Species: Human

Assay Type: Competitive Inhibition

Sensitivity: 15.3 pg/mL

Standard: 3000 pg/mL

Detection range: 46.88-3000 pg/mL

Sample type: Serum, plasma and other biological fluids.

Assay length: 2h

Research Area: Tumor immunity;Endocrinology;Hormone metabolism;

Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Human bMSH protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human bMSH. 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 Human bMSH in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: β-MSH

Species: Human

Assay Type: Competitive Inhibition

Sensitivity: 15.3 pg/mL

Standard: 3000 pg/mL

Detection range: 46.88-3000 pg/mL

Sample type: Serum, plasma and other biological fluids.

Assay length: 2h

Research Area: Tumor immunity;Endocrinology;Hormone metabolism;

Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Human bMSH protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human bMSH. 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 Human bMSH in the samples is then determined by comparing the OD of the samples to the standard curve.