ELK3236-48T, Human UNG(Uracil DNA Glycosylase) ELISA Kit, 48T

ELK3236-48T, Human UNG(Uracil DNA Glycosylase) ELISA Kit, 48T

ELK3237-48T, Human TDG(Thymine DNA Glycosylase) ELISA Kit, 48T

ELK3237-48T, Human TDG(Thymine DNA Glycosylase) ELISA Kit, 48T

ELK3236-96T, Human UNG(Uracil DNA Glycosylase) ELISA Kit, 96T

2.963,10 RON

Human UNG(Uracil DNA Glycosylase) ELISA Kit

SKU
ELK3236-96T

Alternative Names: UDG; UNG1; UNG2; HIGM4

Species: Human

Assay Type: Sandwich

Sensitivity: 0.053 ng/mL

Standard: 10 ng/mL

Detection range: 0.16-10 ng/mL

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

Mai multe informatii
Price 2.490,00 RON (preturile sunt fara TVA)
Description

Alternative Names: UDG; UNG1; UNG2; HIGM4

Species: Human

Assay Type: Sandwich

Sensitivity: 0.053 ng/mL

Standard: 10 ng/mL

Detection range: 0.16-10 ng/mL

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