ELK9816-96T, Rat FHL1(Four And A Half LIM Domains Protein 1) ELISA Kit, 96T

ELK9816-96T, Rat FHL1(Four And A Half LIM Domains Protein 1) ELISA Kit, 96T

ELK9817-96T, EPA(Eicosapentaenoic Acid) ELISA Kit, 96T

ELK9817-96T, EPA(Eicosapentaenoic Acid) ELISA Kit, 96T

ELK9817-48T, EPA(Eicosapentaenoic Acid) ELISA Kit, 48T

2.142,00 RON

EPA(Eicosapentaenoic Acid) ELISA Kit

SKU
ELK9817-48T

Alternative Names: Icosapentaenoic Acid; Timnodonic Acid

Species: General

Assay Type: Competitive Inhibition

Sensitivity: 0.13 ng/mL

Standard: 20 ng/mL

Detection range: 0.31-20 ng/mL

Sample type: serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids

Assay length: 2h

Research Area: Biochemicals

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

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Description

Alternative Names: Icosapentaenoic Acid; Timnodonic Acid

Species: General

Assay Type: Competitive Inhibition

Sensitivity: 0.13 ng/mL

Standard: 20 ng/mL

Detection range: 0.31-20 ng/mL

Sample type: serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids

Assay length: 2h

Research Area: Biochemicals

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