ELK8283-96T, Horse SAA(Serum Amyloid A) ELISA Kit, 96T

ELK8283-96T, Horse SAA(Serum Amyloid A) ELISA Kit, 96T

ELK8284-96T, SB(Stercobilin) ELISA Kit, 96T

ELK8284-96T, SB(Stercobilin) ELISA Kit, 96T

ELK8284-48T, SB(Stercobilin) ELISA Kit, 48T

1.814,75 RON

SB(Stercobilin) ELISA Kit

SKU
ELK8284-48T

Alternative Names: SB

Species: General

Assay Type: Competitive Inhibition

Sensitivity: 0.56 ng/mL

Standard: 100 ng/mL

Detection range: 1.57-100 ng/mL

Sample type: serum, plasma, stool and other biological fluids

Assay length: 2h

Research Area: Metabolic pathway;

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

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Description

Alternative Names: SB

Species: General

Assay Type: Competitive Inhibition

Sensitivity: 0.56 ng/mL

Standard: 100 ng/mL

Detection range: 1.57-100 ng/mL

Sample type: serum, plasma, stool and other biological fluids

Assay length: 2h

Research Area: Metabolic pathway;

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