ELK8390-96T, Rat TLR1(Toll Like Receptor 1) ELISA Kit, 96T

ELK8390-96T, Rat TLR1(Toll Like Receptor 1) ELISA Kit, 96T

ELK8391-96T, Rat MAOB(Monoamine Oxidase B) ELISA Kit, 96T

ELK8391-96T, Rat MAOB(Monoamine Oxidase B) ELISA Kit, 96T

ELK8391-48T, Rat MAOB(Monoamine Oxidase B) ELISA Kit, 48T

2.142,00 RON

Rat MAOB(Monoamine Oxidase B) ELISA Kit

SKU
ELK8391-48T

Alternative Names: MAO-B; Amine oxidase [flavin-containing] B

Species: Rat

Assay Type: Sandwich

Sensitivity: 12.4 pg/mL

Standard: 2000 pg/mL

Detection range: 31.25-2000 pg/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 Rat MAOB. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat MAOB. 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 MAOB, 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 MAOB in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: MAO-B; Amine oxidase [flavin-containing] B

Species: Rat

Assay Type: Sandwich

Sensitivity: 12.4 pg/mL

Standard: 2000 pg/mL

Detection range: 31.25-2000 pg/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 Rat MAOB. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat MAOB. 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 MAOB, 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 MAOB in the samples is then determined by comparing the OD of the samples to the standard curve.