ELK0424-48T, SA(Sialic Acid) ELISA Kit, 48T

ELK0424-48T, SA(Sialic Acid) ELISA Kit, 48T

ELK0425-48T, Human ACAT1(Acetyl Coenzyme A Acetyltransferase 1) ELISA Kit, 48T

ELK0425-48T, Human ACAT1(Acetyl Coenzyme A Acetyltransferase 1) ELISA Kit, 48T

ELK0424-96T, SA(Sialic Acid) ELISA Kit, 96T

2.963,10 RON

SA(Sialic Acid) ELISA Kit

SKU
ELK0424-96T

Alternative Names: SA

Species: General

Assay Type: Competitive Inhibition

Sensitivity: 26.1 µg/mL

Standard: 5000 µg/mL

Detection range: 78.13-5000 µg/mL

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

Assay length: 2.5h

Research Area: Signal transduction;Tumor immunity;Hepatology;

Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with SA protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to SA. 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 SA in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: SA

Species: General

Assay Type: Competitive Inhibition

Sensitivity: 26.1 µg/mL

Standard: 5000 µg/mL

Detection range: 78.13-5000 µg/mL

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

Assay length: 2.5h

Research Area: Signal transduction;Tumor immunity;Hepatology;

Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with SA protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to SA. 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 SA in the samples is then determined by comparing the OD of the samples to the standard curve.