Mouse MI gamma/CXCL9 (Monocyte Interferon Gamma Inducing Factor) ELISA Kit
The Mouse MIγ/CXCL9 (Monocyte Interferon Gamma Inducing Factor) ELISA Kit is a sophisticated tool engineered for precise and quantitative measurement of MIγ/CXCL9 in various biological samples. MIγ/CXCL9, also known as Monocyte Interferon Gamma Inducing Factor, is a significant chemokine involved in immune responses and the recruitment of immune cells, particularly monocytes and T cells, to sites of inflammation. Accurate quantification of MIγ/CXCL9 levels is crucial for understanding its crucial role in mediating immune cell behaviors and regulating immune responses, particularly in the context of inflammatory processes and immune cell recruitment. This ELISA kit provides researchers with a reliable method to analyze the expression levels of MIγ/CXCL9, enabling a deeper exploration of its involvement in immune-related pathways and disease states. Our Mouse MIγ/CXCL9 ELISA Kit ensures exceptional sensitivity and specificity, guaranteeing accurate and reproducible results for your research needs. Manufactured with stringent quality control measures, this kit offers robust and reliable performance, making it an excellent choice for studies focusing on immune cell recruitment, inflammation, and immune response modulation.
Product Name:
Mouse MI gamma/CXCL9 (Monocyte Interferon Gamma Inducing Factor) ELISA Kit
SKU:
AEES00265
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.
