ELK2906-96T, Human IDE(Insulin Degrading Enzyme) ELISA Kit, 96T

ELK2906-96T, Human IDE(Insulin Degrading Enzyme) ELISA Kit, 96T

ELK2907-96T, Human LACRT(Lacritin) ELISA Kit, 96T

ELK2907-96T, Human LACRT(Lacritin) ELISA Kit, 96T

ELK2907-48T, Human LACRT(Lacritin) ELISA Kit, 48T

2.142,00 RON

Human LACRT(Lacritin) ELISA Kit

SKU
ELK2907-48T

Alternative Names: Extracellular glycoprotein lacritin

Species: Human

Assay Type: Sandwich

Sensitivity: 0.63 ng/mL

Standard: 100 ng/mL

Detection range: 1.57-100 ng/mL

Sample type: saliva, tears and other biological fluids

Assay length: 3.5h

Research Area: Immune molecule;

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

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Description

Alternative Names: Extracellular glycoprotein lacritin

Species: Human

Assay Type: Sandwich

Sensitivity: 0.63 ng/mL

Standard: 100 ng/mL

Detection range: 1.57-100 ng/mL

Sample type: saliva, tears and other biological fluids

Assay length: 3.5h

Research Area: Immune molecule;

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