ELK8676-48T, Rat Malonyl CoA (Malonyl Coenzyme A) ELISA Kit, 48T

ELK8676-48T, Rat Malonyl CoA (Malonyl Coenzyme A) ELISA Kit, 48T

ELK8677-48T, Avian bHB(Beta-Hydroxybutyric Acid) ELISA Kit, 48T

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ELK8676-96T, Rat Malonyl CoA (Malonyl Coenzyme A) ELISA Kit, 96T

2.963,10 RON

Rat Malonyl CoA (Malonyl Coenzyme A) ELISA Kit

SKU
ELK8676-96T

Alternative Names: malonyl coenzyme A

Species: Rat

Assay Type: Sandwich

Sensitivity: 0.059 ng/mL

Standard: 10 ng/mL

Detection range: 0.16-10 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 Rat Malonyl CoA. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat Malonyl CoA. 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 Malonyl CoA, 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 Malonyl CoA in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: malonyl coenzyme A

Species: Rat

Assay Type: Sandwich

Sensitivity: 0.059 ng/mL

Standard: 10 ng/mL

Detection range: 0.16-10 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 Rat Malonyl CoA. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat Malonyl CoA. 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 Malonyl CoA, 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 Malonyl CoA in the samples is then determined by comparing the OD of the samples to the standard curve.