ELK8433-48T, Human PP(Pepsin) ELISA Kit, 48T

ELK8433-48T, Human PP(Pepsin) ELISA Kit, 48T

ELK8434-48T, Rat IRS1(Insulin Receptor Substrate 1) ELISA Kit, 48T

ELK8434-48T, Rat IRS1(Insulin Receptor Substrate 1) ELISA Kit, 48T

ELK8433-96T, Human PP(Pepsin) ELISA Kit, 96T

2.963,10 RON

Human PP(Pepsin) ELISA Kit

SKU
ELK8433-96T

Alternative Names: PP; Pepsin

Species: Human

Assay Type: Competitive Inhibition

Sensitivity: 0.93 ng/mL

Standard: 200 ng/mL

Detection range: 3.13-200 ng/mL

Sample type: Serum, plasma and other biological fluids

Assay length: 2h

Research Area: Enzyme & Kinase;Tumor immunity;Gastroenterology;

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

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Description

Alternative Names: PP; Pepsin

Species: Human

Assay Type: Competitive Inhibition

Sensitivity: 0.93 ng/mL

Standard: 200 ng/mL

Detection range: 3.13-200 ng/mL

Sample type: Serum, plasma and other biological fluids

Assay length: 2h

Research Area: Enzyme & Kinase;Tumor immunity;Gastroenterology;

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