ELK3809-96T, Human HPD(4-Hydroxyphenylpyruvate Dioxygenase) ELISA Kit, 96T

ELK3809-96T, Human HPD(4-Hydroxyphenylpyruvate Dioxygenase) ELISA Kit, 96T

ELK3810-96T, Human LECT2(Leukocyte Cell Derived Chemotaxin 2) ELISA Kit, 96T

ELK3810-96T, Human LECT2(Leukocyte Cell Derived Chemotaxin 2) ELISA Kit, 96T

ELK3810-48T, Human LECT2(Leukocyte Cell Derived Chemotaxin 2) ELISA Kit, 48T

2.142,00 RON

Human LECT2(Leukocyte Cell Derived Chemotaxin 2) ELISA Kit

SKU
ELK3810-48T

Alternative Names: Chm-II; Chm2

Species: Human

Assay Type: Sandwich

Sensitivity: 0.32 ng/mL

Standard: 50 ng/mL

Detection range: 0.79-50 ng/mL

Sample type: Serum, plasma and other biological fluids

Assay length: 3.5h

Research Area: Infection immunity;

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 LECT2. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human LECT2. 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 LECT2, 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 LECT2 in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: Chm-II; Chm2

Species: Human

Assay Type: Sandwich

Sensitivity: 0.32 ng/mL

Standard: 50 ng/mL

Detection range: 0.79-50 ng/mL

Sample type: Serum, plasma and other biological fluids

Assay length: 3.5h

Research Area: Infection immunity;

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 LECT2. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human LECT2. 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 LECT2, 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 LECT2 in the samples is then determined by comparing the OD of the samples to the standard curve.