Home > Keywords > DSPE-
| Catalog | name | Description | price |
|---|---|---|---|
| R-C-5683 | DSPE-PEG2K-TRDLVYKDPARPKIQK(FITC) | DSPE, as a core material, can form a stable phospholipid bilayer structure on the surface of nanoparticles, while PEG modification improves the biocompatibility and stability of nanoparticles. TRDLVYKDPARPKIQK is a specific peptide sequence that can specifically bind to specific cell receptors or targets. FITC (fluorescein) is a fluorescent marker that can be covalently linked to DSPE-PEG-TRDLVYKDPARPKIQK, enabling fluorescent labeling of nanoparticles and detection and tracking applications in techniques such as fluorescence microscopy. | price> |
| R-C-7264 | DSPE-PEG2000-SS-R9 | DSPE-PEG-SS-R9,This product combines lipophilicity, hydrophilicity, responsive release, and cell penetration ability, making this composite molecule an ideal drug delivery system. PEG2000 improves the biocompatibility and circulation time of drug carriers, reducing the likelihood of being cleared by the immune system. R9 enhances the entry of drug carriers into target cells,thereby improving the effectiveness of targeted therapy. | price> |
| R-C-7265 | DSPE-SS-PEG2k-PEI1.8K | DSPE-SS-PEG-PEI,This product combines the hydrophobic anchoring of DSPE, hydrophilic protection of PEG,and cationic gene compression ability of PEI,and also achieves responsive drug release through disulfide bonds(SS).Used for loading hydrophobic drugs(such as paclitaxel,doxorubicin)and nucleic acids(such as siRNA, mRNA),PEG prolongs circulation,Polyethyleneimine enhances transfection efficiency. | price> |
| R-C-7266 | DSPE-PEG2000-PA2881 | DSPE-PEG-PA2881,DSPE provides hydrophobic anchoring and can embed into lipid bilayers to form stable structures.PEG endows hydrophilicity and spatial stability,reduces non-specific adsorption,and prolongs cycle time.PA2881 is used for positron emission tomography(PET)imaging,and its preparation involves linking the cyclic peptide Cyclopeptide 66 with the bifunctional chelating agent NOTA and labeling it with radioactive isotopes. | price> |
| R-C-5687 | DSPE-PEG2K-CSTSMLKAC(FITC) | DSPE serves as the core material, capable of forming a stable phospholipid bilayer structure on the surface of nanoparticles or liposomes.PEG2K modification enhances the biocompatibility and stability of the nanoparticles,preventing their rapid clearance by the immune system.The peptide sequence CSTSMLKAC is a specific peptide ligand that can selectively bind to certain cell receptors or targets.FITC is a fluorescent dye that is covalently attached to the DSPE-PEG-CSTSMLKAC conjugate.This allows for the fluorescence labeling of nanoparticles or liposomes,enabling their visualization and tracking using techniques like fluorescence microscopy. | price> |
| R-C-7267 | DSPE-PEG2k-Hyd-NHS | DSPE-PEG-Hyd-NHS,DSPE as a phospholipid skeleton, endows the material with hydrophobic hydrophilic equilibrium properties and can stably embed into the lipid bilayer structure.PEG segments reduce non-specific adsorption through steric hindrance effect,enhancing the cycling stability of the material.Hydrazone bonds act as dynamic covalent bonds and undergo reversible hydrolysis under weakly acidic conditions,achieving environmental responsive regulation.The terminal groups of NHS form stable amide bonds through efficient reactions with amino groups,providing active sites for the coupling of biomolecules. | price> |
| R-C-7268 | DSPE-PEG2K-CRPPR | DSPE-PEG-CRPPR,DSPE as a phospholipid skeleton,endows the material with hydrophobic hydrophilic equilibrium properties and can stably embed into the lipid bilayer structure.PEG segments reduce non-specific adsorption through steric hindrance effect,enhancing the cycling stability of the material.The CRPPR peptide sequence may confer targeting capabilities or enhance cellular interactions. | price> |
| R-C-5689 | DSPE-mPEG350 | 1,2-Distearoyl-sn-Glycero-3-Phosphoethanolamine with conjugated methoxyl poly(ethylene glycol) (DSPE-mPEG) is a linear phospholipid PEG conjugate which has both hydrophilicity and hydrophobility. Pegylated phospholipids are excellent liposome or micelle formation materials that can be used for drug delivery.Pegylation of phospholipids significantly improves the blood circulation time and stability for encapsulated drugs. | price> |
| R-C-7269 | DSPE-TK-PEG2000-LTHVVWL | DSPE-TK-PEG-LTHVVWL,DSPE-TK-PEG-LTHVWL provides an efficient and precise drug delivery system by combining molecules with different functions,enhancing drug targeting,controlled release,and biocompatibility. | price> |
| R-C-7272 | DSPE-Polysarcosine28-Mal | DSPE-Polysarcosine28-Mal(DSPE-Psar28-Mal),DSPE-Polysarcosine28-Mal is a phospholipid polymer conjugate composed of di stearoyl phosphatidylethanolamine (DSPE) and poly (glycine)polymer(Polysarcosine)connected by maleimide(Mal) functional groups The flexibility and low immunogenicity of Polysarosine chains enable the material to exhibit good compatibility and stability in biological systems. | price> |
| R-C-5697 | DSPE-HA | DSPE-Hyaluronic acid,Hyaluronic acid is a naturally occurring polysaccharide found in the extracellular matrix of tissues. It plays various roles in biological processes such as cell adhesion, wound healing, and inflammation regulation. DSPE is a lipid that can form liposomes or micelles when combined with other lipids. The conjugation of HA to DSPE provides the ability to target specific cells or tissues that express hyaluronic acid receptors. This targeted delivery system can be utilized for drug and gene delivery, imaging agents, and tissue engineering scaffolds. | price> |
| R-C-5700 | DSPE-Galactose-FITC | DSPE-Galactose-FITC is commonly used as a probe or label in biological and biomedical research. The galactose moiety allows for specific binding to galactose receptors or lectins on cell surfaces, making it useful for targeting specific cell types.fluorescent dye provides a means to visualize and track the labeled molecules or cells.This conjugate can be incorporated into liposomal formulations or used directly as a probe in various applications, including cell imaging, receptor targeting studies, or drug delivery systems. | price> |
| R-C-5701 | DSPE-PEG2000-Cilomilast | DSPE-PEG-Cilomilast,1, 2-Distearoyl-sn-glycero-3-phosphoethanolamine-Poly(ethylene glycol) (DSPE- PEG) is a widely used phospholipids-polymer conjugate in drug delivery applications.It is a biocompatible,biodegradable and amphiphilic material which can also be functionalized with various biomolecules for specific functions.Cilomilast is a medication that belongs to the class of drugs known as phosphodiesterase-4 (PDE4) inhibitors. | price> |
| R-C-5702 | DSPE-PEG-Transferrin-ICG | DSPE-PEG2000-Transferrin-ICG,DSPE-PEG-Transferrin-ICG can be used as a targeted molecular imaging and drug delivery system. The DSPE and PEG components help to stabilize and improve the pharmacokinetics of the liposomes, while the Transferrin component allows for specific binding to transferrin receptors on target cells, enhancing the uptake of the liposomes by these cells. The ICG component provides near-infrared fluorescence, which can be used for imaging and tracking the liposomes in vivo.This conjugate has potential applications in targeted imaging and therapeutic delivery, especially in the field of cancer research. | price> |
| R-C-5706 | DSPE-PEG2K-cRGDfk | DSPE-PEG-cRGDfk,DSPE-PEG-cRGD,1,2-distearoyl-sn-glycero-3-phosphoethanolamine is a phospholipid derivative commonly used in the formulation of liposomes or lipid-based drug delivery systems.cRGDfk is a peptide sequence derived from the extracellular matrix protein fibronectin. The "c" in cRGDfk indicates that the peptide is cyclic in structure. Such constructs are commonly used in drug delivery systems to enhance the targeting and internalization of drugs by specifically interacting with receptors on target cells. | price> |
| R-C-5707 | DSPE-PEG2000-PLGLAG-protease | DSPE-PEG-PLGLAG-protease,1,2-distearoyl-sn-glycero-3-phosphoethanolamine is a phospholipid derivative commonly used in liposomal formulations and drug delivery systems.PEG is biocompatible polymer often attached to drugs or nanoparticles to improve their stability, solubility, and circulation time in the body.Our product is only used for scientific research and is not suitable for clinical and other human experiments. | price> |
| R-C-5713 | DSPE-PEG2000-bis-5HT | DSPE-PEG-bis-5HT,DSPE-PEG-bis-5-hydroxytrytamine (5HT),DSPE is a type of phospholipid commonly used in the formation of liposomes and lipid-based drug delivery systems.It contains two stearoyl chains and a polar head group consisting of a glycerol backbone and a phosphoethanolamine group.PEG is often added to liposomal formulations to confer stealth properties, prolong circulation time,and improve biocompatibility.Bis-5-hydroxytryptamine(5HT)is a neurotransmitter found in the central nervous system.It plays a crucial role in regulating mood,sleep,and appetite. | price> |
| R-C-5719 | DSPE-DOTA-Gd(III) | Gd(III)DOTA-DSPE,Gd(III)DOTA is a commonly used MRI (magnetic resonance imaging) contrast agent. It contains a chelating ligand,DOTA,which can bind to gadolinium(III) ions.Gadolinium(III) ions have unpaired electrons that generate a strong signal when interacting with magnetic fields, enhancing the contrast in MRI images.DSPE is a lipid derivative commonly used in the formulation of liposomes or lipid nanoparticles. | price> |
| R-C-5721 | DSPE-PEG-Maltotriose hydrate | DSPE-PEG-Maltotriose hydrate,DSPE is a phospholipid that is commonly used in lipid-based drug delivery systems.It provides stability and structure to liposomes and lipid nanoparticles.The PEGylation of a drug carrier can enhance its biocompatibility,prolong circulation time in the bloodstream, and reduce immune response. | price> |
| R-C-5722 | DSPE-PEG350-Maltotriose hydrate | DSPE-PEG-Maltotriose hydrate,DSPE is a phospholipid that is commonly used in lipid-based drug delivery systems.It provides stability and structure to liposomes and lipid nanoparticles.The PEGylation of a drug carrier can enhance its biocompatibility,prolong circulation time in the bloodstream, and reduce immune response.Small molecules are more difficult to produce. | price> |

Items-$0.00

Email:
Tel.:
RuixiBiotechCo.Ltd /KamulinBiotechco.ltd
Add: Room 20F 2002, Meiyuan Building, Yanta District, Xi’ an City, Shaanxi Province 710061 China
Tel: 02988811435
Fax: (86-29)8881-1435
Email: sales@ruixibiotech.com
Web: http://www.ruixibiotech.com


