ELK8580-48T, Pig ADT(Androsterone) ELISA Kit, 48T

ELK8580-48T, Pig ADT(Androsterone) ELISA Kit, 48T

ELK8581-48T, Human HE4(Epididymal protein 4) ELISA Kit, 48T

ELK8581-48T, Human HE4(Epididymal protein 4) ELISA Kit, 48T

ELK8580-96T, Pig ADT(Androsterone) ELISA Kit, 96T

2.475,20 RON

Pig ADT(Androsterone) ELISA Kit

SKU
ELK8580-96T

Alternative Names: 17-Ketosteroid; 17-KS; 3a-Hydroxy-17-Androstanone

Species: Pig

Assay Type: Competitive Inhibition

Sensitivity: 144 pg/mL

Standard: 90000 pg/mL

Detection range: 1406.25-90000 pg/mL

Sample type: serum, plasma and other biological fluids

Assay length: 2h

Research Area: Biochemical research

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

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Description

Alternative Names: 17-Ketosteroid; 17-KS; 3a-Hydroxy-17-Androstanone

Species: Pig

Assay Type: Competitive Inhibition

Sensitivity: 144 pg/mL

Standard: 90000 pg/mL

Detection range: 1406.25-90000 pg/mL

Sample type: serum, plasma and other biological fluids

Assay length: 2h

Research Area: Biochemical research

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