ELK0548-96T, Rat MITF(Microphthalmia Associated Transcription Factor) ELISA Kit, 96T

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ELK0549-96T, Sheep T4(Thyroxine) ELISA Kit, 96T

ELK0549-96T, Sheep T4(Thyroxine) ELISA Kit, 96T

ELK0549-48T, Sheep T4(Thyroxine) ELISA Kit, 48T

1.814,75 RON

Sheep T4(Thyroxine) ELISA Kit

SKU
ELK0549-48T

Alternative Names: 3,5,3',5'-Tetraiodothyronine; L-Thyroxine; Levothyroxine

Species: Sheep

Assay Type: Competitive Inhibition

Sensitivity: 1.81 ng/mL

Standard: 300 ng/mL

Detection range: 4.69-300 ng/mL

Sample type: serum, plasma and other biological fluids

Assay length: 2.5h

Research Area: Endocrinology;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 Sheep T4 protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Sheep T4. 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 Sheep T4 in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: 3,5,3',5'-Tetraiodothyronine; L-Thyroxine; Levothyroxine

Species: Sheep

Assay Type: Competitive Inhibition

Sensitivity: 1.81 ng/mL

Standard: 300 ng/mL

Detection range: 4.69-300 ng/mL

Sample type: serum, plasma and other biological fluids

Assay length: 2.5h

Research Area: Endocrinology;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 Sheep T4 protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Sheep T4. 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 Sheep T4 in the samples is then determined by comparing the OD of the samples to the standard curve.