Human FDP (Fibrinogen Degradation Product) ELISA Kit
The Human FDP (Fibrinogen Degradation Product) ELISA Kit is a powerful tool for accurately measuring levels of FDP in human samples such as serum, plasma, and cell culture supernatants. This kit offers exceptional sensitivity and specificity, ensuring dependable and consistent results for a variety of research purposes.Fibrinogen degradation products are important indicators of fibrinolysis and coagulation activity in the body. Elevated levels of FDP are associated with conditions such as disseminated intravascular coagulation (DIC), sepsis, and thrombosis, making this ELISA kit invaluable for the study of these diseases and the development of potential therapies. Overall, the Human FDP ELISA Kit offers researchers a reliable and precise method for quantifying FDP levels, helping to advance our understanding of coagulation disorders and supporting the discovery of new treatment options.
Product Name:
Human FDP (Fibrinogen Degradation Product) ELISA Kit
SKU:
HUES03089
Size:
96 Assays
Detection Method:
Colorimetric method, ELISA, Sandwich
Assay type:
Sandwich-ELISA
Assay time:
3 h 30 min
Sensitivity:
0.94 ng/mL
Detection range:
1.56-100 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.
