ELK7898-96T, rT3(Reverse Triiodothyronine) ELISA Kit, 96T

ELK7898-96T, rT3(Reverse Triiodothyronine) ELISA Kit, 96T

ELK7899-96T, SCT(Salmon Calcitonin) ELISA Kit, 96T

ELK7899-96T, SCT(Salmon Calcitonin) ELISA Kit, 96T

ELK7899-48T, SCT(Salmon Calcitonin) ELISA Kit, 48T

1.814,75 RON

SCT(Salmon Calcitonin) ELISA Kit

SKU
ELK7899-48T

Alternative Names: CGRP; Salcatonin

Species: General

Assay Type: Competitive Inhibition

Sensitivity: 31.4 pg/mL

Standard: 20000 pg/mL

Detection range: 312.5-20000 pg/mL

Sample type: biological agents

Assay length: 2h

Research Area: Metabolic pathway;Endocrinology;Hormone metabolism;Bone metabolism;

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

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Description

Alternative Names: CGRP; Salcatonin

Species: General

Assay Type: Competitive Inhibition

Sensitivity: 31.4 pg/mL

Standard: 20000 pg/mL

Detection range: 312.5-20000 pg/mL

Sample type: biological agents

Assay length: 2h

Research Area: Metabolic pathway;Endocrinology;Hormone metabolism;Bone metabolism;

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