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ELK Biotechnology
SKU:ELK10278
Human NGB(Neuroglobin) ELISA Kit
Human NGB(Neuroglobin) ELISA Kit
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Alternative Names: Neuroglobin
Assay Type: Sandwich
Sensitivity: 0.11 ng/mL
standard: 20 ng/mL
Detection range: 0.32-20 ng/mL
Sample type: serum, plasma and other biological fluids
Assay length: 3.5h
Research Area: Metabolic pathway;Neuro science;
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 NGB. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human NGB. 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 NGB, 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 NGB in the samples is then determined by comparing the OD of the samples to the standard curve.
UniProt ID: Q9NPG2
Assay Type: Sandwich
Sensitivity: 0.11 ng/mL
standard: 20 ng/mL
Detection range: 0.32-20 ng/mL
Sample type: serum, plasma and other biological fluids
Assay length: 3.5h
Research Area: Metabolic pathway;Neuro science;
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 NGB. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human NGB. 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 NGB, 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 NGB in the samples is then determined by comparing the OD of the samples to the standard curve.
UniProt ID: Q9NPG2
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