ELK8660-96T, Mouse FABP1(Fatty Acid Binding Protein 1, Liver) ELISA Kit, 96T

ELK8660-96T, Mouse FABP1(Fatty Acid Binding Protein 1, Liver) ELISA Kit, 96T

ELK8661-96T, Human BA(Butyric Acid) ELISA Kit, 96T

ELK8661-96T, Human BA(Butyric Acid) ELISA Kit, 96T

ELK8661-48T, Human BA(Butyric Acid) ELISA Kit, 48T

1.814,75 RON

Human BA(Butyric Acid) ELISA Kit

SKU
ELK8661-48T

Alternative Names: Propanecarboxylic Acid; Butanoic Acid

Species: Human

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: Drug synthesis

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

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: Drug synthesis

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