Product phospholipids -phospholipid-peg-customization

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Catalog	name	Description	price
R-C-5917	DOPE-PEG350-CGYEQDPWGVRYGC	DOPE-PEG-CGYEQDPWGVRYGC,DOPE is a type of phospholipid that can form liposomes or liposomal nanoparticles,providing a stable and biocompatible platform for drug delivery.PEG is often used in drug delivery systems to increase stability, extend circulation time,reduce immunogenicity, and prevent nonspecific interactions with proteins and other biomolecules.CGYEQDPWGVRYGC,The peptide sequence is designed to specifically bind to a target receptor present on cancer cells.	price>
R-C-7499	DSPE-PEG-Mal-Cys-NGR	Cys-NGR-MAL-PEG-DSPE,The hydrophobic chains of DSPE can be inserted into the lipid bilayer structure of carriers such as liposomes and nanoparticles to achieve surface modification of materials;PEG segments can improve the water solubility and biocompatibility of the carrier.Cys NGR refers to the NGR peptide(Asn Gly Arg)with cysteine(Cys)extension.The NGR peptide can specifically recognize CD13 receptors(αvβ 3 integrin related)highly expressed in tumor neovascular endothelial cells,achieving active targeting.The introduced Cys provides thiol groups,facilitating efficient coupling with DSPE-PEG-Mal.This product is only for scientific research and cannot be used on the human body.	price>
R-C-7500	DSPE-PEG-VHPKQHRC	VHPKQHRC-PEG-DSPE,DSPE-PEG-VCAM-1,DSPE is a hydrophobic membrane anchoring unit that stably embeds into the lipid carrier membrane structure;PEG is a flexible hydrophilic spacer arm that provides steric hindrance,reduces non-specific adsorption,and prolongs cycling time; VHPKQHRC is an octapeptide sequence that specifically targets VCAM-1(vascular cell adhesion molecule 1),endowing it with active targeting ability.This design integrates membrane anchoring, long cycling,and targeted recognition,and is the core material for VCAM-1 related research.This product is only for scientific research and cannot be used on the human body.	price>
R-C-7501	DSPE-PEG-SS-DBCO	DBCO-PEG-SS-DSPE,The core function of DSPE-SS-PEG-DBCO lies in its dual regulation of environmental responsiveness and chemical modification.The molecule uses DSPE as its hydrophobic core,and its long-chain alkyl structure endows it with the ability to embed into lipid bilayers,forming a stable nanostructure foundation.The PEG chain is connected to DSPE through a reducible disulfide bond(SS).Under physiological conditions, the disulfide bond remains stable, but can be broken in a reducing microenvironment (such as a high concentration of glutathione in cells),achieving controllable detachment of the PEG layer.The DBCO group is located at the end of PEG and serves as an active site for bioorthogonal reactions.It can efficiently bind with azides through copper free click through reaction(SPAAC)without the need for catalysts to achieve specific modifications.This product is only for scientific research and cannot be used on the human body.	price>
R-C-7506	DSPE-PEG-Cys-RVG29	RVG29-Cys-PEG-DSPE,DSPE-PEG-Cys-RVG29 is a targeted conjugated molecule composed of phospholipids(DSPE),polyethylene glycol(PEG),and cysteine modified RVG29 peptide,widely used to construct intelligent drug delivery systems that can penetrate the blood-brain barrier (BBB).RVG29 is a 29 amino acid derived peptide derived from the glycoprotein of rabies virus (usually with the sequence YTIWSPVTAARAAIGLSTAGGLGGVGG).Its N-terminus or side chain is modified with cysteine(Cys),introducing a free thiol group(-SH)for specific click chemical coupling with a maleimide functionalized vector.This product is only for scientific research and cannot be used on the human body.	price>
R-C-5944	DSPE-PEG2k-CGPLGVRGDK-DBCO	DBCO(Dibenzylcyclooctyne) reagents can be used to label azide-modified biomolecules spontaneous without the need for toxic Cu catalysts.The reaction of azides with strained alkynes,such as cyclooctynes, readily forms a triazole product without the need for a toxic catalystPEGylation can increase solubility and stability and reduce immunogenicity of peptides and proteins.It can also suppress the non-specific binding of charged molecules to the modified surfaces.It can also couple various peptides.	price>
R-C-5965	Gd-DOTA-C6-DSPE	DSPE-C6-DOTA-Gd,Gd-DOTA-C6-DSPE is often used in the formulation of lipid-based nanoparticles for drug delivery,imaging, or theranostic applications (combined diagnostic and therapeutic functions).The Gd-DOTA complex provides the contrast agent properties for imaging, and the DSPE component facilitates the incorporation of the molecule into lipid-based nanoparticle systems.	price>
R-C-6043	DSPE-PEG5000-CFP10(71-85)	DSPE-PEG-CFP10(71-85),Polyethylene glycol liposomes were used to form high-quality materials.It can be used for drug delivery,gene transfection and vaccine delivery.Pegylated phospholipids can significantly improve blood circulation time and stabilize drug encapsulation.CFP10(71–85)is a biological active peptide.(CFP1071–85,that elicited IFN-γ production and CTL activity by both CD4+ and CD8+ T cells from persons expressing multiple MHC class II and class I molecules).	price>
R-C-6248	FITC-CGFECVRQCPERC-PEG2k-DSPE	DSPE-PEG-CGFECVRQCPERC-FITC,DSPE-PEG is a long circulating liposome membrane,formation of micelles in water dispersion,the critical micelle concentration(CMC)ratio of surfactant is 102 times lower,so the drug stability is better,even by hemodilution,can maintain the integrity of the micelle particle,has certain targeting,easy accumulation in solid tumors.Fluorescein labeled DSPE PEG products emitted green fluorescence and can be easily detected with regular fluorescent instrucments.It can couple various peptides,such as CGFECVRQCPERC.	price>
R-C-6347	DSPE-PEG2000-tLyP-1(CGNKRTR)	DSPE-PEG-CGNKRTR,DSPE-PEG-tLyp1,DSPE-PEG-tLyP-1(CGNKRTR)is a molecular construct commonly used in the field of targeted drug delivery.DSPE(1,2-distearoyl-sn-glycero-3-phosphoethanolamine)is a type of phospholipid that is often used in the formulation of lipid-based nanoparticles or liposomes for drug delivery applications.tLyP-1 is a specific peptide sequence(CGNKRTR)that has been designed for tumor-targeting applications.It has an affinity for certain receptors that are overexpressed in tumor vasculature,allowing for targeted delivery of therapeutic agents to tumor tissues.	price>

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