MILLIPLEX MAP & Cell Signaling Pathways
Cell signaling, often called signal transduction, is a complex system of communication that enables cells to perceive, communicate with and respond to their microenvironment. This communication may occur as a result of:
- Direct cell-to-cell contact
- Effects that are induced when a receptor that has been activated by a ligand interacts directly with other proteins inside the cell
- Cellular changes resulting from complex signal transduction pathways involving kinase receptors that, when bound to a ligand, become phosphorylated
Signaling | 391,660 | |
Protein Kinase | 324,422 | |
Phosphorylation | 166,174 | 53,262 |
Acetylation | 1,882 | 2,788 |
Methylation | 2,329 | 832 |
Ubiquitin | 24,504 | 488 |
SUMO | 1,518 | 386 |
The binding of a growth factor to its receptor on the membrane triggers a cascade of kinase activation, resulting in the phosphorylation of a transcription factor, which binds to DNA in the nucleus that promotes specific expression of genes associated with, for example, cell division.
These multi-component cell signaling pathways are so complex that often there is feedback, signal amplification, and interactions between more than one signal and among several signaling pathways.
The cell’s ability to respond to its environment is essential for normal development, cellular repair and immunity and is the basis of homeostasis. Errors in these pathways, caused by mutations that may result in constitutive expression or total inhibition of protein transcription, are responsible for such diseases as diabetes, autoimmune disorders and cancer.
Millipore is proud to provide you with two MILLIPLEX MAP cell signaling technologies, both using the Luminex xMAP platform:
Cell Signaling Assays | EpiQuant Cell Signaling Assays |
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Both technologies offer you the ability to investigate simultaneously the expression of intracellular total or phosphorylated proteins involved in multi-pathway signaling or focused in a specific pathway. Choose the technology that best meets your needs.

