The AlphaLISA® Mouse/Rat C-C Motif Chemokine 2/Monocyte Chemoattractant Protein 1 (CCL2/MCP1) Detection Kit is designed for detection and quantitation of mouse or rat CCL2/MCP1 in buffered solution or cell culture medium in a homogeneous (no-wash steps, no separation steps) assay. Mouse CCL2/MCP1 can be quantitatively measured in mouse serum. The analyte in this kit is mouse CCL2/MCP1.
For research use only. Not for use in diagnostic procedures.
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Mouse and rat C-C Motif Chemokine 2 (CCL2) or Monocyte Chemoattractant Protein 1 (MCP1) contain 125 amino acids and are glycosylated. CCL2 is part of the CXC subfamily of cytokines. In mouse, fibroblasts, tumor cells, smooth muscle cells, endothelial cells, and mononuclear phagocytes can produce CCL2 either constitutively or upon stimulation. CCL2 displays chemotactic activity for monocytes and basophils, but not for neutrophils or eosinophils. It also regulates adhesion molecule expression and cytokine production in mouse monocytes. CCL2 has been implicated in the pathogenesis of diseases characterized by monocytic infiltrates, like psoriasis, rheumatoid arthritis and atherosclerosis. CCL2 is considered as an important biomarker in cardiovascular diseases.
AlphaLISA technology allows the detection of molecules of interest in a no-wash, highly sensitive, quantitative assay. In an AlphaLISA assay, a biotinylated anti-analyte antibody binds to the Streptavidin-coated Donor beads while another anti-analyte antibody is conjugated to AlphaLISA Acceptor beads. In the presence of the analyte, the beads come into close proximity. The excitation of the Donor beads causes the release of singlet oxygen molecules that triggers a cascade of energy transfer in the Acceptor beads, resulting in a sharp peak of light emission at 615 nm.
|Assay Target Class||Cytokine|
|Experimental Type||In vitro|
|Product Brand Name||AlphaLISA|
|Shipping Condition||Blue Ice|
|Unit Size||5,000 assay points|
The AlphaLISA® assay is a homogeneous immunoassay alternative to classical ELISA. AlphaLISA assays were originally utilized to detect analytesin cell cultures upernatants or serum/plasma samples.