ELK9177-96T, Human CoQ10(Coenzyme Q10) ELISA Kit, 96T

ELK9177-96T, Human CoQ10(Coenzyme Q10) ELISA Kit, 96T

ELK9178-96T, LTD4(Leukotriene D4) ELISA Kit, 96T

ELK9178-96T, LTD4(Leukotriene D4) ELISA Kit, 96T

ELK9178-48T, LTD4(Leukotriene D4) ELISA Kit, 48T

2.142,00 RON

LTD4(Leukotriene D4) ELISA Kit

SKU
ELK9178-48T

Alternative Names: LTD4

Species: General

Assay Type: Competitive Inhibition

Sensitivity: 0.082 ng/mL

Standard: 20 ng/mL

Detection range: 0.31-20 ng/mL

Sample type: serum, plasma and other biological fluids

Assay length: 3.5h

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 LTD4 protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to LTD4. 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 LTD4 in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: LTD4

Species: General

Assay Type: Competitive Inhibition

Sensitivity: 0.082 ng/mL

Standard: 20 ng/mL

Detection range: 0.31-20 ng/mL

Sample type: serum, plasma and other biological fluids

Assay length: 3.5h

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 LTD4 protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to LTD4. 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 LTD4 in the samples is then determined by comparing the OD of the samples to the standard curve.