ELK8898-48T, Human HAGH(Hydroxyacylglutathione Hydrolase) ELISA Kit, 48T

ELK8898-48T, Human HAGH(Hydroxyacylglutathione Hydrolase) ELISA Kit, 48T

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ELK8898-96T, Human HAGH(Hydroxyacylglutathione Hydrolase) ELISA Kit, 96T

2.963,10 RON

Human HAGH(Hydroxyacylglutathione Hydrolase) ELISA Kit

SKU
ELK8898-96T

Alternative Names: GLO2; GLX2; GLXII; HAGH1; Glyoxalase II; Hydroxyacyl Glutathione Hydrolase

Species: Human

Assay Type: Sandwich

Sensitivity: 0.119 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 HAGH. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human HAGH. 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 HAGH, 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 HAGH in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: GLO2; GLX2; GLXII; HAGH1; Glyoxalase II; Hydroxyacyl Glutathione Hydrolase

Species: Human

Assay Type: Sandwich

Sensitivity: 0.119 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 HAGH. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human HAGH. 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 HAGH, 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 HAGH in the samples is then determined by comparing the OD of the samples to the standard curve.