ELK5665-96T, Dog EPO(Erythropoietin) ELISA Kit, 96T

ELK5665-96T, Dog EPO(Erythropoietin) ELISA Kit, 96T

ELK5666-96T, Rat MT1(Metallothionein 1) ELISA Kit, 96T

ELK5666-96T, Rat MT1(Metallothionein 1) ELISA Kit, 96T

ELK5666-48T, Rat MT1(Metallothionein 1) ELISA Kit, 48T

2.142,00 RON

Rat MT1(Metallothionein 1) ELISA Kit

SKU
ELK5666-48T

Alternative Names: MT1A; MT1S; MTC

Species: Rat

Assay Type: Sandwich

Sensitivity: 14.1 pg/mL

Standard: 2000 pg/mL

Detection range: 31.25-2000 pg/mL

Sample type: Serum, plasma, tissue homogenates and other biological fluids

Assay length: 3.5h

Research Area: Signal transduction;Tumor immunity;

Test principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Rat MT1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat MT1. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Rat MT1, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. 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 MT1 in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: MT1A; MT1S; MTC

Species: Rat

Assay Type: Sandwich

Sensitivity: 14.1 pg/mL

Standard: 2000 pg/mL

Detection range: 31.25-2000 pg/mL

Sample type: Serum, plasma, tissue homogenates and other biological fluids

Assay length: 3.5h

Research Area: Signal transduction;Tumor immunity;

Test principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Rat MT1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat MT1. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Rat MT1, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. 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 MT1 in the samples is then determined by comparing the OD of the samples to the standard curve.