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Catalog	name	Description	price
R-C-4046	DSPE-PEG350-Alkyne	1,2-distearoyl-sn-glycero-3-phosphoethanolamine-polyethylene glycol-Thiol is a linear heterobifunctional PEGylation reagent with a DSPE phospholipid and a thiol group.It is a useful self-assembling reagent to prepare PEGylated liposome or micelle while also providing a thiol group for conjugation with thiol-containing molecules.It is often used in targeted drug delivery with the lipid bilayer to improve drug solubility,the PEG to provide stealth property, extend circulation half-life and reduce non-specific protein binding or cell adhesion,and the acid group to bioconjugate targeting molecules including antibody,aptamer,protein,and peptide.	price>
R-R-5726	Non-PEGylated Magnetic Liposomes	Non-PEGylated magnetic liposomes are nanoparticles formed from lipid bilayers that encapsulate drugs and incorporate magnetic materials, typically iron oxides (like magnetite or maghemite). Without polyethylene glycol (PEG) modifications, these liposomes exhibit enhanced interaction with biological systems, potentially leading to faster clearance from circulation. Their size usually ranges from 100 to several hundred nanometers, making them suitable for targeted drug delivery and biomedical applications. The magnetic properties enable controlled drug release and precise targeting via external magnetic fields, making them particularly valuable in cancer therapy, gene delivery, and imaging modalities like MRI.	price>
R-C-4047	DSPE-polyethylene glycol550-Alkyne	1,2-distearoyl-sn-glycero-3-phosphoethanolamine-polyethylene glycol-Thiol is a linear heterobifunctional PEGylation reagent with a DSPE phospholipid and a thiol group. It is a useful self-assembling reagent to prepare PEGylated liposome or micelle while also providing a thiol group for conjugation with thiol-containing molecules. It is often used in targeted drug delivery with the lipid bilayer to improve drug solubility, the PEG to provide stealth property, extend circulation half-life and reduce non-specific protein binding or cell adhesion, and the acid group to bioconjugate targeting molecules including antibody, aptamer, protein, and peptide.	price>
R-R-5727	PEGylated Magnetic Liposomes	PEGylated magnetic liposomes are sophisticated nanocarriers composed of lipid bilayers that encapsulate therapeutic agents while incorporating magnetic nanoparticles, such as iron oxide, for enhanced targeting capabilities. The addition of polyethylene glycol (PEG) on the liposomal surface improves biocompatibility, increases circulation time in the bloodstream, and reduces immunogenicity. These liposomes typically range from 100 to 200 nanometers in diameter, enabling efficient drug delivery to specific tissues, particularly in cancer therapy. The magnetic properties allow for targeted delivery and controlled release of encapsulated drugs when subjected to an external magnetic field, enhancing therapeutic efficacy while minimizing side effects. Additionally, the use of PEG helps stabilize the liposomes in biological environments, addressing issues of drug leakage and aggregation. Overall, PEGylated magnetic liposomes represent a promising approach in nanomedicine, combining the advantages of targeted therapy with improved pharmacokinetics for various biomedical applications.	price>
R-C-4048	Alkyne-PEG750-DSPE	1,2-distearoyl-sn-glycero-3-phosphoethanolamine-polyethylene glycol-Thiol is a linear heterobifunctional PEGylation reagent with a DSPE phospholipid and a thiol group. It is a useful self-assembling reagent to prepare PEGylated liposome or micelle while also providing a thiol group for conjugation with thiol-containing molecules. It is often used in targeted drug delivery with the lipid bilayer to improve drug solubility, the PEG to provide stealth property, extend circulation half-life and reduce non-specific protein binding or cell adhesion, and the acid group to bioconjugate targeting molecules including antibody, aptamer, protein, and peptide.	price>
R-R-5728	Non-PEGylated DOTA Liposomes for Remote Loading Radioactive Divalent Cations	DOTA encapsulated liposomes are used for remote loading of radioactive divalent ions such as radioactive copper into the liposomes. Cationic ions will not pass through the membrane if there is no pH gradient. Divalent ion will cross the liposome membrane only when there is a flux of proton across of the lipid membrane. Due to the difference in the pH inside and outside of the liposomes, there will be a constant flux of proton from inside of the liposomes to outside of the liposomes. Due to this flux, divalent cations move in the opposite direction from outside to inside of liposomes. Liposomes are thermodynamically stable structures and not very permeable to divalent cations after they are formed. If there is no pH gradient, the divalent cations cannot move from outside to inside of the liposomes, where they will remain outside and won’t cross the membrane. The driving force for remote loading in proton gradient. The radioactive divalent copper is externally added to the liposomes. The divalent ion passes the membrane using pH gradient method and chelates DOTA.	price>
R-C-4049	DSPE-PEG350-CHO	Polyethylene glycol(PEG)compounds contain a polyether unit.They are generally biocompatible,non-toxic and stable in both organic and aqueous solutions,and so are extensively used in biological applications,as well as nanotechnology and materials research.	price>
R-R-5729	PEGylated DOTA Liposomes for Remote Loading Radioactive Divalent	CDOTA encapsulated liposomes are used for remote loading of radioactive divalent ions such as radioactive copper into the liposomes. Cationic ions will not pass through the membrane if there is no pH gradient. Divalent ion will cross the liposome membrane only when there is a flux of proton across of the lipid membrane. Due to the difference in the pH inside and outside of the liposomes, there will be a constant flux of proton from inside of the liposomes to outside of the liposomes. Due to this flux, divalent cations move in the opposite direction from outside to inside of liposomes. Liposomes are thermodynamically stable structures and not very permeable to divalent cations after they are formed. If there is no pH gradient, divalent cations cannot move from outside to inside of the liposomes, where they will remain outside and won’t cross the membrane. The driving force for remote loading in proton gradient. The radioactive divalent copper is externally added to the liposomes. The divalent ion passes the membrane using pH gradient method and chelates DOTA.	price>
R-C-4050	DSPE-polyethylene glycol550-CHO	Polyethylene glycol(PEG)compounds contain a polyether unit.They are generally biocompatible,non-toxic and stable in both organic and aqueous solutions,and so are extensively used in biological applications,as well as nanotechnology and materials research.	price>
R-R-5730	DSPE-PEG-YGMSPRNRTGSNKPNCIRAIWPTFTEPDG	DSPE-PEG-YGMSPRNRTGSNKPNCIRAIWPTFTEPDG effectively combines the advantages of liposomal encapsulation, prolonged half-life due to PEGylation, and precise targeting via the peptide sequence, making it a promising candidate for drug delivery systems aimed at improving therapeutic outcomes in cancer and other diseases.	price>
R-C-4051	CHO-PEG750-DSPE	Polyethylene glycol(PEG)compounds contain a polyether unit.They are generally biocompatible,non-toxic and stable in both organic and aqueous solutions,and so are extensively used in biological applications,as well as nanotechnology and materials research.	price>
R-R-5731	(PEGylated)Doxosome-Doxorubicin Liposomes	PEGylated Doxorubicin Liposomes are a type of non surface reactive doxorubicin liposome.The formulation of this doxorubicin liposome is PEGylated and is only used for research purposes and laboratory animal injection. The doxorubicin drug has been remotely loaded into liposomes via ammonium sulfate gradient. Surface reactive doxorubicin liposomes suitable for coupling various antibodies, proteins, peptides, and ligands are also available.	price>
R-C-4052	DSPE-PEG350-OPSS	1,2-Distearoyl-sn-glycero-3-phosphoethanolamine(DSPE)-poly(ethylene glycol) with conjugated orthopyridyl disulfide (OPSS or PDP)(DSPE-PEG-OPSS)is a linear heterobifunctional PEGylation reagent with a DSPE phospholipid and a orthopyridyl disulfide.DSPE-PEG-OPSS, is an 18 carbon phospholipid PEG conjugate which has both hydrophilicity and hydrophobility.It is a useful self-assembling reagent to prepare PEGylated liposome or micelle while also providing a thiol or cysteine reactive maleimide group.	price>
R-C-5952	PTB7 Mw 80000-200000 PDI ≤3.0 CAS:1266549-31-8	PTB7 is a semiconducting polymer used in organic photovoltaics with an energy efficiency of 9.15%.It can act as an electron donor with narrow optical band gaps and excellent π-π conjugation while forming a nanocomposite with fullerenes.	price>
R-R-5732	(PEGylated) Doxosome Control-Doxorubicin Liposomes	(PEGylated) Doxosome Control-Doxorubicin Liposomes is a control formulation of PEGylated Doxorubicin liposomes. This formulation is similar in size and lipid composition to PEGylated Doxorubicin liposomes but does not contain the Doxorubicin drug. This formulation is for research purposes and injection into laboratory animals only.	price>
R-C-4053	DSPE-polyethylene glycol550-OPSS	1,2-Distearoyl-sn-glycero-3-phosphoethanolamine(DSPE)-poly(ethylene glycol) with conjugated orthopyridyl disulfide (OPSS or PDP)(DSPE-PEG-OPSS)is a linear heterobifunctional PEGylation reagent with a DSPE phospholipid and a orthopyridyl disulfide.DSPE-PEG-OPSS, is an 18 carbon phospholipid PEG conjugate which has both hydrophilicity and hydrophobility.It is a useful self-assembling reagent to prepare PEGylated liposome or micelle while also providing a thiol or cysteine reactive maleimide group.	price>
R-C-5953	SY-PPV,Super Yellow CAS:26009-24-5	Super yellow light emitting PPV copolymer can form a thin film of poly(1,4-phenylenevinylene)(PPV)with high efficiencies.It has conjugated polymers as the backbone that can be soluble in water upon the incorporation of lipophilic solubilizing linkers.	price>
R-R-5733	Doxorubicin liposomes for post-insertion (non-PEGylated)	Doxorubicin is a widely used chemotherapeutic agent that has been formulated into liposomal drug delivery systems to enhance its therapeutic efficacy while reducing systemic toxicity. Liposomes are spherical vesicles composed of lipid bilayers that can encapsulate hydrophilic and hydrophobic drugs. Non-PEGylated doxorubicin liposomes represent a specific formulation that does not utilize polyethylene glycol (PEG) to modify the liposomal surface.	price>
R-C-4054	OPSS-PEG750-DSPE	1,2-Distearoyl-sn-glycero-3-phosphoethanolamine(DSPE)-poly(ethylene glycol) with conjugated orthopyridyl disulfide (OPSS or PDP)(DSPE-PEG-OPSS)is a linear heterobifunctional PEGylation reagent with a DSPE phospholipid and a orthopyridyl disulfide.DSPE-PEG-OPSS, is an 18 carbon phospholipid PEG conjugate which has both hydrophilicity and hydrophobility.It is a useful self-assembling reagent to prepare PEGylated liposome or micelle while also providing a thiol or cysteine reactive maleimide group.	price>
R-C-5954	FITC-DITWDQLWDLMK-PEG2000-DSPE	DSPE-PEG-Esbp(DITWDQLWDLMK)-FITC,Pegylated phospholipids are excellent liposome formation materials that can be used for drug delivery,gene transfection and vaccine delivery as well.Pegylation of phospholipids significantly improves the blood circulation time and stability for encapsulated drugs. These materials can also be used for targeted drug delivery by modifying their surfaces with targeting ligands such as antibodies, peptidesEsbp(DITWDQLWDLMK).	price>

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