ELK6962-96T, Human CCT2(Chaperonin Containing TCP1, Subunit 2) ELISA Kit, 96T

ELK6962-96T, Human CCT2(Chaperonin Containing TCP1, Subunit 2) ELISA Kit, 96T

ELK6963-96T, Human UACA(Uveal Autoantigen With Coiled Coil Domains And Ankyrin Repeats) ELISA Kit, 96T

ELK6963-96T, Human UACA(Uveal Autoantigen With Coiled Coil Domains And Ankyrin Repeats) ELISA Kit, 96T

ELK6963-48T, Human UACA(Uveal Autoantigen With Coiled Coil Domains And Ankyrin Repeats) ELISA Kit, 48T

2.142,00 RON

Human UACA(Uveal Autoantigen With Coiled Coil Domains And Ankyrin Repeats) ELISA Kit

SKU
ELK6963-48T

Alternative Names: NUCLING

Species: Human

Assay Type: Sandwich

Sensitivity: 0.108 ng/mL

Standard: 20 ng/mL

Detection range: 0.32-20 ng/mL

Sample type: Tissue homogenates and other biological fluids.

Assay length: 3.5h

Research Area: Signal transduction;

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 Human UACA. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human UACA. 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 Human UACA, 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 Human UACA in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: NUCLING

Species: Human

Assay Type: Sandwich

Sensitivity: 0.108 ng/mL

Standard: 20 ng/mL

Detection range: 0.32-20 ng/mL

Sample type: Tissue homogenates and other biological fluids.

Assay length: 3.5h

Research Area: Signal transduction;

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 Human UACA. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human UACA. 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 Human UACA, 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 Human UACA in the samples is then determined by comparing the OD of the samples to the standard curve.