ELK8183-96T, Human Anti-SNCa(Anti-Synuclein Alpha Antibody) ELISA Kit, 96T

ELK8183-96T, Human Anti-SNCa(Anti-Synuclein Alpha Antibody) ELISA Kit, 96T

ELK8184-96T, ALCAR(Acetylcarnitine) ELISA Kit, 96T

ELK8184-96T, ALCAR(Acetylcarnitine) ELISA Kit, 96T

ELK8184-48T, ALCAR(Acetylcarnitine) ELISA Kit, 48T

1.814,75 RON

ALCAR(Acetylcarnitine) ELISA Kit

SKU
ELK8184-48T

Alternative Names: Acetyl-L-carnitine

Species: General

Assay Type: Competitive Inhibition

Sensitivity: 25.2 ng/mL

Standard: 5000 ng/mL

Detection range: 78.13-5000 ng/mL

Sample type: serum, plasma and other biological fluids

Assay length: 2h

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

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Description

Alternative Names: Acetyl-L-carnitine

Species: General

Assay Type: Competitive Inhibition

Sensitivity: 25.2 ng/mL

Standard: 5000 ng/mL

Detection range: 78.13-5000 ng/mL

Sample type: serum, plasma and other biological fluids

Assay length: 2h

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