DSPE-PEG2000-Maleimide free acid is a phospholipid-PEG conjugate designed for targeted liposome and nanoparticle applications. This compound exploits the amphiphilic properties of DSPE to integrate into lipid bilayers, enabling effective delivery systems. Through thiol-maleimide click chemistry, it allows for the covalent attachment of ligands, such as antibodies, peptides, or proteins, facilitating targeted therapy. DSPE-PEG2000-Maleimide free acid is particularly valuable in research concerning breast cancer, lymphoma, and inherited retinal degeneration.
DSPE-PEG2000-Maleimide free acid is a phospholipid-PEG conjugate designed for targeted liposome and nanoparticle applications. This compound exploits the amphiphilic properties of DSPE to integrate into lipid bilayers, enabling effective delivery systems. Through thiol-maleimide click chemistry, it allows for the covalent attachment of ligands, such as antibodies, peptides, or proteins, facilitating targeted therapy. DSPE-PEG2000-Maleimide free acid is particularly valuable in research concerning breast cancer, lymphoma, and inherited retinal degeneration.
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