ELK0855-48T, Human PPP1R16B(Protein Phosphatase 1, Regulatory Subunit 16B) ELISA Kit, 48T

ELK0855-48T, Human PPP1R16B(Protein Phosphatase 1, Regulatory Subunit 16B) ELISA Kit, 48T

ELK0856-48T, Human Cit(Citrulline) ELISA Kit, 48T

ELK0856-48T, Human Cit(Citrulline) ELISA Kit, 48T

ELK0855-96T, Human PPP1R16B(Protein Phosphatase 1, Regulatory Subunit 16B) ELISA Kit, 96T

2.963,10 RON

Human PPP1R16B(Protein Phosphatase 1, Regulatory Subunit 16B) ELISA Kit

SKU
ELK0855-96T

Alternative Names: ANKRD4; TIMAP

Species: Human

Assay Type: Sandwich

Sensitivity: 0.051 ng/mL

Standard: 10 ng/mL

Detection range: 0.16-10 ng/mL

Sample type: Tissue homogenates, cell lysates and other biological fluids

Assay length: 3.5h

Research Area: Metabolic pathway;

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 PPP1R16B. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human PPP1R16B. 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 PPP1R16B, 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 PPP1R16B in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: ANKRD4; TIMAP

Species: Human

Assay Type: Sandwich

Sensitivity: 0.051 ng/mL

Standard: 10 ng/mL

Detection range: 0.16-10 ng/mL

Sample type: Tissue homogenates, cell lysates and other biological fluids

Assay length: 3.5h

Research Area: Metabolic pathway;

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 PPP1R16B. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human PPP1R16B. 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 PPP1R16B, 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 PPP1R16B in the samples is then determined by comparing the OD of the samples to the standard curve.