ELK2654-96T, Human Des(Desmin) ELISA Kit, 96T

ELK2654-96T, Human Des(Desmin) ELISA Kit, 96T

ELK2655-96T, Rat Des(Desmin) ELISA Kit, 96T

ELK2655-96T, Rat Des(Desmin) ELISA Kit, 96T

ELK2655-48T, Rat Des(Desmin) ELISA Kit, 48T

2.142,00 RON

Rat Des(Desmin) ELISA Kit

SKU
ELK2655-48T

Alternative Names: CMD1I; CSM1; CSM2; Intermediate Filament Protein

Species: Rat

Assay Type: Sandwich

Sensitivity: 0.9 ng/mL

Standard: 150 ng/mL

Detection range: 2.35-150 ng/mL

Sample type: Serum, plasma, tissue homogenates and other biological fluids.

Assay length: 3.5h

Research Area: Signal transduction;Metabolic pathway;Bone metabolism;

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

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Description

Alternative Names: CMD1I; CSM1; CSM2; Intermediate Filament Protein

Species: Rat

Assay Type: Sandwich

Sensitivity: 0.9 ng/mL

Standard: 150 ng/mL

Detection range: 2.35-150 ng/mL

Sample type: Serum, plasma, tissue homogenates and other biological fluids.

Assay length: 3.5h

Research Area: Signal transduction;Metabolic pathway;Bone metabolism;

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