Human GDF11 (Growth Differentiation Factor 11) ELISA Kit
The Human GDF11 (Growth Differentiation Factor 11) ELISA Kit is designed for the precise measurement of GDF11 levels in human serum, plasma, and cell culture supernatants. With its high sensitivity and specificity, this kit provides accurate and reproducible results, making it an ideal tool for various research applications.GDF11 is a key protein that regulates cell growth and differentiation, playing a critical role in developmental processes and tissue regeneration. Its dysregulation has been linked to various diseases such as cardiovascular disorders, musculoskeletal conditions, and aging-related pathologies, making it a valuable biomarker for studying these conditions and exploring potential therapeutic interventions.For more information or to purchase the Human GDF11 ELISA Kit, please visit www.assaygenie.com/human-gdf11-growth-differentiation-factor-11-elisa-kit-hues02855/.
Product Name:
Human GDF11 (Growth Differentiation Factor 11) ELISA Kit
SKU:
HUES02855
Size:
96 Assays
Detection Method:
Colorimetric method, ELISA, Sandwich
Assay type:
Sandwich-ELISA
Assay time:
3 h 30 min
Sensitivity:
9.38 pg/mL
Detection range:
15.63-1000 pg/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.
