ELK4164-48T, Human SQLE(Squalene Epoxidase) ELISA Kit, 48T

ELK4164-48T, Human SQLE(Squalene Epoxidase) ELISA Kit, 48T

ELK4165-48T, Human SGSH(N-Sulfoglucosamine Sulfohydrolase) ELISA Kit, 48T

ELK4165-48T, Human SGSH(N-Sulfoglucosamine Sulfohydrolase) ELISA Kit, 48T

ELK4164-96T, Human SQLE(Squalene Epoxidase) ELISA Kit, 96T

2.963,10 RON

Human SQLE(Squalene Epoxidase) ELISA Kit

SKU
ELK4164-96T

Alternative Names: SE; ERG1; Squalene monooxygenase

Species: Human

Assay Type: Sandwich

Sensitivity: 0.114 ng/mL

Standard: 20 ng/mL

Detection range: 0.32-20 ng/mL

Sample type: Tissue homogenates, cell lysates and other biological fluids

Assay length: 3.5h

Research Area: Enzyme & Kinase;

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

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Description

Alternative Names: SE; ERG1; Squalene monooxygenase

Species: Human

Assay Type: Sandwich

Sensitivity: 0.114 ng/mL

Standard: 20 ng/mL

Detection range: 0.32-20 ng/mL

Sample type: Tissue homogenates, cell lysates and other biological fluids

Assay length: 3.5h

Research Area: Enzyme & Kinase;

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