ELK9557-48T, Horse KL(Klotho) ELISA Kit, 48T

ELK9557-48T, Horse KL(Klotho) ELISA Kit, 48T

ELK9558-48T, Mouse MDGA1(MAM domain-containing glycosylphosphatidylinositol anchor protein 1) ELISA Kit, 48T

ELK9558-48T, Mouse MDGA1(MAM domain-containing glycosylphosphatidylinositol anchor protein 1) ELISA Kit, 48T

ELK9557-96T, Horse KL(Klotho) ELISA Kit, 96T

2.963,10 RON

Horse KL(Klotho) ELISA Kit

SKU
ELK9557-96T

Alternative Names: Kl ; KLOT; Klotho peptide

Species: Horse

Assay Type: Sandwich

Sensitivity: 0.113 ng/mL

Standard: 20 ng/mL

Detection range: 0.32-20 ng/mL

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

Assay length: 3.5h

Research Area: Metabolic pathway;

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

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Description

Alternative Names: Kl ; KLOT; Klotho peptide

Species: Horse

Assay Type: Sandwich

Sensitivity: 0.113 ng/mL

Standard: 20 ng/mL

Detection range: 0.32-20 ng/mL

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

Assay length: 3.5h

Research Area: Metabolic pathway;

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