Human MI gamma/CXCL9 (Monocyte Interferon Gamma Inducing Factor) ELISA Kit
The Human MIγ/CXCL9 (Monocyte Interferon Gamma-Inducing Factor) ELISA Kit is a specialized assay intended for the precise quantification of Monocyte Interferon Gamma-Inducing Factor, also known as MIγ or CXCL9, in various biological samples. MIγ/CXCL9 is a chemokine that plays a crucial role in immune responses and cell signaling by attracting monocytes and activated T cells to sites of inflammation. Accurate measurement of MIγ/CXCL9 levels is essential for understanding its role in immune modulation, inflammation, and immune cell recruitment. This ELISA kit offers exceptional sensitivity and specificity, ensuring accurate and reproducible results. Manufactured with strict adherence to quality control standards, the MIγ/CXCL9 ELISA Kit delivers robust performance while being user-friendly, making it an excellent choice for both research and clinical applications. Researchers can rely on this kit to quantify MIγ/CXCL9 efficiently and effectively in their studies.
Product Name:
Human MI gamma/CXCL9 (Monocyte Interferon Gamma Inducing Factor) ELISA Kit
SKU:
AEES00098
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.
