ELK8174-48T, BA(Butyric Acid) ELISA Kit, 48T

ELK8174-48T, BA(Butyric Acid) ELISA Kit, 48T

ELK8175-48T, ADP(Adenosine Diphosphate) ELISA Kit, 48T

ELK8175-48T, ADP(Adenosine Diphosphate) ELISA Kit, 48T

ELK8174-96T, BA(Butyric Acid) ELISA Kit, 96T

2.475,20 RON

BA(Butyric Acid) ELISA Kit

SKU
ELK8174-96T

Alternative Names: Propanecarboxylic Acid; Butanoic Acid

Species: General

Assay Type: Competitive Inhibition

Sensitivity: 51.5 pg/mL

Standard: 10000 pg/mL

Detection range: 156.25-10000 pg/mL

Sample type: Biological agents

Assay length: 2h

Research Area: Signal transduction;Metabolic pathway;Endocrinology;

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

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Description

Alternative Names: Propanecarboxylic Acid; Butanoic Acid

Species: General

Assay Type: Competitive Inhibition

Sensitivity: 51.5 pg/mL

Standard: 10000 pg/mL

Detection range: 156.25-10000 pg/mL

Sample type: Biological agents

Assay length: 2h

Research Area: Signal transduction;Metabolic pathway;Endocrinology;

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