Date published: 2025-12-11

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CD43 Inhibitors

CD43, also known as sialophorin, is a highly glycosylated transmembrane protein predominantly expressed on the surface of leukocytes, where it plays a multifaceted role in mediating various aspects of the immune response. This protein is involved in the regulation of cell adhesion, migration, and the activation of T cells, contributing to its critical function in the immune system's ability to respond to pathogens. The extensive glycosylation of CD43 imparts a negative charge to the cell surface, which aids in the repulsion of other negatively charged cells, thereby modulating cell-cell interactions within the immune system. Additionally, CD43 extends outward from the cell membrane, acting as a physical barrier that modulates the accessibility of the cell surface to external factors, including pathogens and signaling molecules. This unique structure and function of CD43 underscore its importance in the immune surveillance and response mechanisms, facilitating the dynamic interplay between immune cells and their environment. The inhibition of CD43 function can significantly impact the immune system's efficacy, altering leukocyte behavior and compromising the body's defense mechanisms against infections and diseases. Inhibition can occur through various mechanisms, including the binding of antibodies or other molecules to CD43, which can block its interaction with ligands and signaling partners, thereby hindering its role in cell adhesion and migration. Additionally, genetic modifications or pharmacological agents that reduce the expression of CD43 on the cell surface can also inhibit its function, affecting the immune cell's ability to respond to inflammatory signals and migrate to sites of infection or injury. Furthermore, alterations in the glycosylation pattern of CD43 can modify its structural properties and interactions with other molecules, potentially inhibiting its normal function and impacting the immune response. Understanding the mechanisms by which CD43 can be inhibited offers valuable insights into its role in immune regulation and the potential consequences of its dysregulation, highlighting the complexity of immune system modulation and the critical function of CD43 in maintaining immune homeostasis.

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