ELK2859-96T, Human CD99(Cluster Of Differentiation 99) ELISA Kit, 96T

ELK2859-96T, Human CD99(Cluster Of Differentiation 99) ELISA Kit, 96T

ELK2860-96T, Human GLa(Galactosidase Alpha) ELISA Kit, 96T

ELK2860-96T, Human GLa(Galactosidase Alpha) ELISA Kit, 96T

ELK2860-48T, Human GLa(Galactosidase Alpha) ELISA Kit, 48T

2.142,00 RON

Human GLa(Galactosidase Alpha) ELISA Kit

SKU
ELK2860-48T

Alternative Names: GALA; GL-A; Alpha-D-Galactoside Galactohydrolase; Alpha-D-Galactosidase A; Melibiase; Agalsidase

Species: Human

Assay Type: Sandwich

Sensitivity: 0.6 ng/mL

Standard: 100 ng/mL

Detection range: 1.57-100 ng/mL

Sample type: serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids

Assay length: 3.5h

Research Area: Enzyme & Kinase;Metabolic pathway;

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

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Description

Alternative Names: GALA; GL-A; Alpha-D-Galactoside Galactohydrolase; Alpha-D-Galactosidase A; Melibiase; Agalsidase

Species: Human

Assay Type: Sandwich

Sensitivity: 0.6 ng/mL

Standard: 100 ng/mL

Detection range: 1.57-100 ng/mL

Sample type: serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids

Assay length: 3.5h

Research Area: Enzyme & Kinase;Metabolic pathway;

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