ELK9739-96T, Rat KYNA(Kynurenic Acid) ELISA Kit, 96T

ELK9739-96T, Rat KYNA(Kynurenic Acid) ELISA Kit, 96T

ELK9740-96T, Rat Trp(Tryptophan) ELISA Kit, 96T

ELK9740-96T, Rat Trp(Tryptophan) ELISA Kit, 96T

ELK9740-48T, Rat Trp(Tryptophan) ELISA Kit, 48T

1.814,75 RON

Rat Trp(Tryptophan) ELISA Kit

SKU
ELK9740-48T

Alternative Names: Trp

Species: Rat

Assay Type: Competitive Inhibition

Sensitivity: 0.62 µg/mL

Standard: 100 µg/mL

Detection range: 1.57-100 µg/mL

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

Assay length: 2h

Research Area: Enzyme & Kinase;

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

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Description

Alternative Names: Trp

Species: Rat

Assay Type: Competitive Inhibition

Sensitivity: 0.62 µg/mL

Standard: 100 µg/mL

Detection range: 1.57-100 µg/mL

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

Assay length: 2h

Research Area: Enzyme & Kinase;

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