ELK6424-96T, Rat CPB1(Carboxypeptidase B1, Tissue) ELISA Kit, 96T

ELK6424-96T, Rat CPB1(Carboxypeptidase B1, Tissue) ELISA Kit, 96T

ELK6425-96T, Rat IDE(Insulin Degrading Enzyme) ELISA Kit, 96T

ELK6425-96T, Rat IDE(Insulin Degrading Enzyme) ELISA Kit, 96T

ELK6425-48T, Rat IDE(Insulin Degrading Enzyme) ELISA Kit, 48T

2.142,00 RON

Rat IDE(Insulin Degrading Enzyme) ELISA Kit

SKU
ELK6425-48T

Alternative Names: Insulysin; Insulin Protease; Abeta-degrading protease; Insulinase

Species: Rat

Assay Type: Sandwich

Sensitivity: 0.112 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;Metabolic pathway;Endocrinology;Cardiovascular biology;

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

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Description

Alternative Names: Insulysin; Insulin Protease; Abeta-degrading protease; Insulinase

Species: Rat

Assay Type: Sandwich

Sensitivity: 0.112 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;Metabolic pathway;Endocrinology;Cardiovascular biology;

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