Catalog name Description price
R-C-4969 DSPE-PEG350-Cyclodextrin-b β- Cyclodextrin, also known as cyclomaltose or cyclodextrin, is abbreviated as β- CD, which is extracted from starch by microbial enzymes, consists of 7 glucose residues β- A ring formed by the combination of 1,4-neneneba glycoside bond, with a relative molecular weight of 1135. price>
R-C-4970 dspe-polyethylene-glycol550-cyclodextrin-b β- Cyclodextrin, also known as cyclomaltose or cyclodextrin, is abbreviated as β- CD, which is extracted from starch by microbial enzymes, consists of 7 glucose residues β- A ring formed by the combination of 1,4-neneneba glycoside bond, with a relative molecular weight of 1135. price>
R-C-4971 Cyclodextrin-b-PEG750-DSPE β- Cyclodextrin, also known as cyclomaltose or cyclodextrin,is abbreviated as β- CD,which is extracted from starch by microbial enzymes,consists of 7 glucose residues β- A ring formed by the combination of 1,4-neneneba glycoside bond,with a relative molecular weight of 1135. price>
R-C-4973 DSPE-PEG-LPS Polyethylene glycol (PEG)-coupled DSPE is hydrophilic and can be used for drug delivery,gene transfection and biomolecular modification.PEGylation of phospholipid significantly improved the blood circulation time and stability of capsule drugs.Lipopolysaccharide is a substance buried on the outermost side of the cell wall of Gram negative bacteria, which can completely activate the activity of human immune cells. price>
R-C-4974 DSPE-PEG350-LPS Polyethylene glycol (PEG)-coupled DSPE is hydrophilic and can be used for drug delivery,gene transfection and biomolecular modification.PEGylation of phospholipid significantly improved the blood circulation time and stability of capsule drugs.Lipopolysaccharide is a substance buried on the outermost side of the cell wall of Gram negative bacteria, which can completely activate the activity of human immune cells. price>
R-C-4975 DSPE-polyethylene glycol550-LPS Polyethylene glycol (PEG)-coupled DSPE is hydrophilic and can be used for drug delivery,gene transfection and biomolecular modification.PEGylation of phospholipid significantly improved the blood circulation time and stability of capsule drugs.Lipopolysaccharide is a substance buried on the outermost side of the cell wall of Gram negative bacteria, which can completely activate the activity of human immune cells. price>
R-C-4976 lipopolysaccharide-PEG750-DSPE Polyethylene glycol (PEG)-coupled DSPE is hydrophilic and can be used for drug delivery,gene transfection and biomolecular modification.PEGylation of phospholipid significantly improved the blood circulation time and stability of capsule drugs.Lipopolysaccharide is a substance buried on the outermost side of the cell wall of Gram negative bacteria, which can completely activate the activity of human immune cells. price>
R-C-4977 DSPE-PEG-FPBA DSPE phosphonate, as a pharmaceutical excipient, has the functions of emulsification and drug solubilization, and is an important material for slow and controlled release pharmaceutical preparations such as liposomes, fat assessments, nanoparticle in recent years. Common modification methods include: introducing polymers to improve the blood circulation time and disintegration time of formulations; Introducing immune factors to enhance targeting; Introduce markers for diagnosis and tracking. price>
R-C-4978 DSPE-PEG350-FPBA DSPE phosphonate, as a pharmaceutical excipient, has the functions of emulsification and drug solubilization, and is an important material for slow and controlled release pharmaceutical preparations such as liposomes, fat assessments, nanoparticle in recent years. Common modification methods include: introducing polymers to improve the blood circulation time and disintegration time of formulations; Introducing immune factors to enhance targeting; Introduce markers for diagnosis and tracking. price>
R-C-4979 DSPE-polyethylene glycol550-FPBA DSPE phosphonate, as a pharmaceutical excipient, has the functions of emulsification and drug solubilization, and is an important material for slow and controlled release pharmaceutical preparations such as liposomes, fat assessments, nanoparticle in recent years. Common modification methods include: introducing polymers to improve the blood circulation time and disintegration time of formulations; Introducing immune factors to enhance targeting; Introduce markers for diagnosis and tracking. price>