ELK7925-48T, Arg(Arginine) ELISA Kit, 48T

ELK7925-48T, Arg(Arginine) ELISA Kit, 48T

ELK7926-48T, ADT(Androsterone) ELISA Kit, 48T

ELK7926-48T, ADT(Androsterone) ELISA Kit, 48T

ELK7925-96T, Arg(Arginine) ELISA Kit, 96T

2.475,20 RON

Arg(Arginine) ELISA Kit

SKU
ELK7925-96T

Alternative Names: (S)-2-Amino-5-Guanidinopentanoic Acid

Species: General

Assay Type: Competitive Inhibition

Sensitivity: 0.51 µg/mL

Standard: 100 µg/mL

Detection range: 1.57-100 µg/mL

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

Assay length: 2h

Research Area: Metabolic pathway;Nutrition metabolism;

Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Arg protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Arg. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added. 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 Arg in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: (S)-2-Amino-5-Guanidinopentanoic Acid

Species: General

Assay Type: Competitive Inhibition

Sensitivity: 0.51 µg/mL

Standard: 100 µg/mL

Detection range: 1.57-100 µg/mL

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

Assay length: 2h

Research Area: Metabolic pathway;Nutrition metabolism;

Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Arg protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Arg. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added. 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 Arg in the samples is then determined by comparing the OD of the samples to the standard curve.