ELK0569-96T, Human C1QTNF7(C1q And Tumor Necrosis Factor Related Protein 7) ELISA Kit, 96T

ELK0569-96T, Human C1QTNF7(C1q And Tumor Necrosis Factor Related Protein 7) ELISA Kit, 96T

ELK056ES-96T, EasyStep Rat T4(Thyroxine) ELISA Kit, 96T

ELK056ES-96T, EasyStep Rat T4(Thyroxine) ELISA Kit, 96T

ELK056ES-48T, EasyStep Rat T4(Thyroxine) ELISA Kit, 48T

2.689,40 RON

EasyStep Rat T4(Thyroxine) ELISA Kit

SKU
ELK056ES-48T

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

Species: Rat

Assay Type: Competitive Inhibition

Sensitivity: 7 ng/mL

Standard: 600 ng/mL

Detection range: 9.38-600 ng/mL

Sample type: Serum, plasma

Assay length: 1.5h

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 Rat T4 antigen, and the Rat T4 standard plate wells that pre-coated using protein-related techniques are provided separately. Standard/Sample Diluent Buffer or samples are added to the appropriate microtiter plate wells ,then added a HRP-conjugated antibody specific to Rat T4 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 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: Rat

Assay Type: Competitive Inhibition

Sensitivity: 7 ng/mL

Standard: 600 ng/mL

Detection range: 9.38-600 ng/mL

Sample type: Serum, plasma

Assay length: 1.5h

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 Rat T4 antigen, and the Rat T4 standard plate wells that pre-coated using protein-related techniques are provided separately. Standard/Sample Diluent Buffer or samples are added to the appropriate microtiter plate wells ,then added a HRP-conjugated antibody specific to Rat T4 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 T4 in the samples is then determined by comparing the OD of the samples to the standard curve.