ELK4600-48T, Human GDA(Guanine Deaminase) ELISA Kit, 48T

ELK4600-48T, Human GDA(Guanine Deaminase) ELISA Kit, 48T

ELK4601-48T, Human HS2ST1(Heparan Sulfate-2-O-Sulfotransferase 1) ELISA Kit, 48T

ELK4601-48T, Human HS2ST1(Heparan Sulfate-2-O-Sulfotransferase 1) ELISA Kit, 48T

ELK4600-96T, Human GDA(Guanine Deaminase) ELISA Kit, 96T

2.963,10 RON

Human GDA(Guanine Deaminase) ELISA Kit

SKU
ELK4600-96T

Alternative Names: CYPIN; Guanase; Guanine aminase; Guanine aminohydrolase; p51-nedasin

Species: Human

Assay Type: Sandwich

Sensitivity: 0.129 ng/mL

Standard: 20 ng/mL

Detection range: 0.32-20 ng/mL

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

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Description

Alternative Names: CYPIN; Guanase; Guanine aminase; Guanine aminohydrolase; p51-nedasin

Species: Human

Assay Type: Sandwich

Sensitivity: 0.129 ng/mL

Standard: 20 ng/mL

Detection range: 0.32-20 ng/mL

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