ELK8708-96T, Goat IGF1(Insulin Like Growth Factor 1) ELISA Kit, 96T

ELK8708-96T, Goat IGF1(Insulin Like Growth Factor 1) ELISA Kit, 96T

ELK8709-96T, Goat MDA(Malondialdehyde) ELISA Kit, 96T

ELK8709-96T, Goat MDA(Malondialdehyde) ELISA Kit, 96T

ELK8709-48T, Goat MDA(Malondialdehyde) ELISA Kit, 48T

1.814,75 RON

Goat MDA(Malondialdehyde) ELISA Kit

SKU
ELK8709-48T

Alternative Names: Malondialdehyde; MDA

Species: Goat

Assay Type: Competitive Inhibition

Sensitivity: 5.39 pg/mL

Standard: 1000 pg/mL

Detection range: 15.63-1000 pg/mL

Sample type: serum, plasma and other biological fluids

Assay length: 2h

Research Area: Metabolic pathway;Hepatology;Hormone metabolism;

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

Mai multe informatii
Price 1.525,00 RON (preturile sunt fara TVA)
Description

Alternative Names: Malondialdehyde; MDA

Species: Goat

Assay Type: Competitive Inhibition

Sensitivity: 5.39 pg/mL

Standard: 1000 pg/mL

Detection range: 15.63-1000 pg/mL

Sample type: serum, plasma and other biological fluids

Assay length: 2h

Research Area: Metabolic pathway;Hepatology;Hormone metabolism;

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