Product phospholipids -phosphadylethanolamine-pe

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Catalog	name	Description	price
R-C-5620	DSPE-PCB	DSPE-PCB20 had the same ability to enhance the serum stability of lipoplexes. However, quite different from the PEGylation, zwitterionic DSPE-PCB20 could offer stability without interfering with the siRNA encapsulation efficiency and endosomal/lysosomal escape ability of lipoplexes, which was favorable for the systemic delivery of siRNA.	price>
R-C-7205	DSPE-PEG-FA-Cy3	PEG endows with water solubility and biocompatibility.The presence of PEG reduces the immunogenicity of DSPE-PEG-FA,prevents serum protein adsorption,thereby reducing non-specific adsorption and improving the stability and bioavailability of drugs in vivo. Folic acid is used to target cells with high expression of folate receptors.Its core function is to achieve targeted delivery of tumor cells through folate receptors,while utilizing the fluorescence properties of CY3 for real-time tracking.	price>
R-C-7206	DSPE-PEG-TAT-FITC	DSPE-PEG-YGRKKRRQRRR-FITC,DSPE-PEG-TAT-FITC is a multifunctional nanomaterial that combines phospholipids(DSPE),polyethylene glycol(PEG), transmembrane peptides(TAT),and fluorescent dyes(FITC).It is mainly used for targeted drug delivery and fluorescence imaging.Its core structure works synergistically through hydrophobic anchoring,hydrophilic stability,and biometric recognition functions to achieve efficient cell penetration and visual tracking.	price>
R-C-7210	DPPE-FA	FA-DPPE,1,2-dipalmitoyl-sn-glycero-3-phosphoethanolamine-Folic acid-Folic acid(DPPE-FA)is a targeted drug delivery material formed by the chemical bond between 1,2-dipalmitoyl-sn-glycerin-3-phosphoethanolamine(DPPE)and folic acid.The DPPE in its core structure provides lipid bilayer stability,while the folate portion actively targets tumor cells by specifically binding to folate receptors(such as FRα).	price>
R-C-7211	DSPE-pSar25-Maleimide	DSPE-pSar-Maleimide is a lipid derivative mainly used in the construction of drug delivery systems,such as the preparation of lipid nanoparticles(LNP),which achieve targeted ligand coupling through specific reaction between maleimide groups and thiol groups(-SH).	price>
R-C-7217	DSPE-PEG-DSS6	DSS6-PEG-DSPE,DSPE-PEG-DSS6 is a composite molecule composed of phospholipids(DSPE),polyethylene glycol(PEG),and bone targeting peptide DSS6,mainly used for bone targeted drug delivery and bone tissue repair. Its core structure achieves precise targeting and efficient delivery through the synergistic effect of three parts.The DSS6 peptide consists of six Asp-Ser-Ser amino acid repeat sequences and can specifically recognize hydroxyapatite(HAp)in bone tissue.	price>
R-C-7218	DOPE-PEG-DSS6	DSS6-PEG-DOPE,DOPE provides hydrophobic anchor points(containing two 18 carbon unsaturated fatty acid chains),while PEG chains form hydrophilic brush like structures, endowing the material with anti protein adsorption ability and stability.The DSS6 peptide consists of six Asp-Ser-Ser amino acid repeat sequences and can specifically recognize hydroxyapatite(HAp)in bone tissue.	price>
R-C-7219	DLPE-PEG-DSS6	DSS6-PEG-DLPE,DLPE-PEG is a combination of February cinnamoyl phosphatidylethanolamine(DLPE)and polyethylene glycol(PEG),which combines the stability of phospholipids with the water solubility and biocompatibility of PEG.It is widely used in drug delivery,nanotechnology,and other fields.The DSS6 peptide consists of six Asp-Ser-Ser amino acid repeat sequences and can specifically recognize hydroxyapatite (HAp)in bone tissue.	price>
R-C-7231	DOPE-LA	LA-DOPE,1,2-Dioleoyl-sn-glycero-3-phosphoethanolamine-lipoic acid(DOPE-LA)is a functionalized phospholipid that combines lipoic acid(LA)with DOPE through chemical modification.Lipoic acid, as a potent antioxidant,can enhance the stability and targeting of DOPE,making it suitable for drug delivery,gene transfection,and biological imaging fields.	price>
R-C-7232	DOPE-SS-PEG-NHS	DOPE-SS-PEG2000-NHS,DOPE-SS-PEG2K-NHS integrates the membrane affinity of phospholipids,the stable protective effect of polyethylene glycol,the reduction responsiveness of disulfide bonds,and the reactivity of NHS ester groups.Its amphiphilic structure allows it to spontaneously form micelles or vesicles in aqueous phase,and the critical micelle concentration decreases with increasing PEG chain length.Disulfide bonds are sensitive to redox environments and can be broken under the action of reducing agents such as DTT and glutathione, releasing loaded substances,NHS ester groups are sensitive to water and should be stored away from light at -20℃ to prevent hydrolysis.	price>

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