ELK6976-96T, Rat SGPP1(Sphingosine-1-Phosphate Phosphatase 1) ELISA Kit, 96T

ELK6976-96T, Rat SGPP1(Sphingosine-1-Phosphate Phosphatase 1) ELISA Kit, 96T

ELK6977-96T, Rat CALD(Caldesmon) ELISA Kit, 96T

ELK6977-96T, Rat CALD(Caldesmon) ELISA Kit, 96T

ELK6977-48T, Rat CALD(Caldesmon) ELISA Kit, 48T

2.142,00 RON

Rat CALD(Caldesmon) ELISA Kit

SKU
ELK6977-48T

Alternative Names: CALD1; CDM; H-CAD; L-CAD; NAG22

Species: Rat

Assay Type: Sandwich

Sensitivity: 0.104 ng/mL

Standard: 20 ng/mL

Detection range: 0.32-20 ng/mL

Sample type: Tissue homogenates and other biological fluids.

Assay length: 3.5h

Research Area: Metabolic pathway;Developmental science;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 CALD. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat CALD. 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 CALD, 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 CALD in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: CALD1; CDM; H-CAD; L-CAD; NAG22

Species: Rat

Assay Type: Sandwich

Sensitivity: 0.104 ng/mL

Standard: 20 ng/mL

Detection range: 0.32-20 ng/mL

Sample type: Tissue homogenates and other biological fluids.

Assay length: 3.5h

Research Area: Metabolic pathway;Developmental science;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 CALD. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat CALD. 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 CALD, 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 CALD in the samples is then determined by comparing the OD of the samples to the standard curve.