The Human NRG-4 (Neuregulin-4) ELISA Kit is a specialized assay designed for the precise measurement of neuregulin-4 levels in human biological samples such as serum, plasma, and cell culture supernatants. This kit offers exceptional sensitivity and specificity, ensuring accurate and consistent results for a variety of research applications.Neuregulin-4 is a key signaling protein that plays a critical role in various biological processes, including cardiomyocyte function, lipid metabolism, and neuronal development. Dysregulation of neuregulin-4 has been linked to diseases such as heart failure, obesity, and neurological disorders, making it a valuable biomarker for studying these conditions and exploring potential therapeutic interventions.With its advanced technology and reliability, the Human NRG-4 ELISA Kit is an essential tool for researchers seeking to unravel the complex mechanisms involving neuregulin-4 and its implications in human health and disease.
Product Name:
Human NRG-4 (Neuregulin 4) ELISA Kit
SKU:
HUES02018
Size:
96 Assays
Detection Method:
Colorimetric method, ELISA, Sandwich
Assay type:
Sandwich-ELISA
Assay time:
3 h 30 min
Sensitivity:
0.47 ng/mL
Detection range:
0.78-50 ng/mL
Reovery:
80%-120%
This ELISA kit uses the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to the target protein. Standards or samples are added to the micro ELISA plate wells and bind to the immobilized antibody. A biotinylated detection antibody specific to the target protein is then added, followed by Avidin-Horseradish Peroxidase (HRP) conjugate. Free components are washed away. The substrate solution is added to each well, resulting in a color change. Only wells containing the target protein, detection antibody, and HRP conjugate will develop a blue color. The reaction is terminated by the addition of stop solution, resulting in a yellow color. The optical density (OD) is measured at 450 nm ± 2 nm. The OD value is directly proportional to the concentration of the target protein in the sample and is determined using a standard curve.
