The Human IL-24 (Interleukin-24) ELISA Kit is a reliable and accurate tool for detecting IL-24 levels in human samples such as serum, plasma, and cell culture supernatants. With high sensitivity and specificity, this kit provides consistent and reproducible results, making it ideal for a wide range of research applications.IL-24 is a cytokine that plays a crucial role in immune responses and inflammation. It has been implicated in various diseases, including cancer, autoimmune disorders, and infectious diseases. By measuring IL-24 levels, researchers can gain valuable insights into the underlying mechanisms of these conditions and potentially identify new therapeutic targets.Overall, the Human IL-24 ELISA Kit is a valuable resource for researchers studying immune responses, inflammation, and disease pathology. Its high-quality components and performance ensure accurate and reliable results, making it an essential tool for advancing scientific knowledge in the field.
Product Name:
Human IL-24 ELISA Kit
SKU:
HUES03294
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.
