Human PLAU/uPA (Urokinase-Type Plasminogen Activator) CLIA Kit
The Human PLAU (UPA) Urokinase-type Plasminogen Activator CLIA Kit is a cutting-edge tool designed for the precise measurement of PLAU levels in human samples such as serum, plasma, and cell culture supernatants. With its exceptional sensitivity and specificity, this kit delivers dependable and reproducible results, making it an invaluable asset for various research purposes.PLAU, also known as Urokinase-type Plasminogen Activator, plays a vital role in processes such as fibrinolysis, cell migration, and tissue remodeling. Increased PLAU levels have been linked to various diseases including cancer, inflammatory disorders, and cardiovascular diseases. Therefore, detecting and quantifying PLAU levels can provide valuable insights for studying these conditions and developing targeted therapies.Overall, the Human PLAU (UPA) Urokinase-type Plasminogen Activator CLIA Kit is a must-have tool for researchers seeking to explore the role of PLAU in health and disease. Get your kit today and unlock new possibilities in your research endeavors.
Product Name:
Human PLAU/uPA (Urokinase-Type Plasminogen Activator) CLIA Kit
SKU:
HUES00991
Size:
96 Assays
Detection Method:
Chemiluminescence
Assay type:
Sandwich-CLIA
Assay time:
3 h 30 min
Sensitivity:
9.38 pg/mL
Detection range:
15.63-1000 pg/mL
Reovery:
80%-120%
This kit uses a sandwich chemiluminescence immunoassay (CLIA) principle. The microplate is pre-coated with an antibody specific to the target protein. Standards or samples are added to the wells and bind to the immobilized antibody. A biotinylated detection antibody is then added, followed by HRP-conjugated streptavidin to form a sandwich complex. After washing to remove unbound components, a chemiluminescent substrate is added. The HRP enzyme catalyzes a light-emitting reaction. The intensity of the emitted light is directly proportional to the concentration of the target protein in the sample. The signal is measured using a luminometer, and the concentration of the analyte is calculated based on a standard curve.
