ELK5019-48T, Human TAP(Trypsinogen Activation Peptide) ELISA Kit, 48T

ELK5019-48T, Human TAP(Trypsinogen Activation Peptide) ELISA Kit, 48T

ELK5020-48T, Human UST2(Urotensin 2) ELISA Kit, 48T

ELK5020-48T, Human UST2(Urotensin 2) ELISA Kit, 48T

ELK5019-96T, Human TAP(Trypsinogen Activation Peptide) ELISA Kit, 96T

2.963,10 RON

Human TAP(Trypsinogen Activation Peptide) ELISA Kit

SKU
ELK5019-96T

Alternative Names: Trypsinogen Activation Peptide

Species: Human

Assay Type: Competitive Inhibition

Sensitivity: 54.1 pg/mL

Standard: 10000 pg/mL

Detection range: 156.25-10000 pg/mL

Sample type: serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids

Assay length: 2h

Research Area: Infection immunity;Immune molecule;Hepatology;

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

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Description

Alternative Names: Trypsinogen Activation Peptide

Species: Human

Assay Type: Competitive Inhibition

Sensitivity: 54.1 pg/mL

Standard: 10000 pg/mL

Detection range: 156.25-10000 pg/mL

Sample type: serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids

Assay length: 2h

Research Area: Infection immunity;Immune molecule;Hepatology;

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