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Catalog | name | Description | price |
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R-M2-9746 | DWFKAFYDKVAEKFKEAF | DWFKAFYDKVAEKFKEAF is a synthetic peptide composed of polar, basic, hydrophobic, and aromatic residues, suggesting potential roles in biomolecular interactions, antimicrobial activity, or self-assembly. | price> |
R-M2-9747 | KLGFFKR-CY5.5 | KLGFFKR-Cy5.5/KLGFFKR,Cy5.5 labed/Cy5.5-KLGFFKR has been used to visualize tumor calcification, a process that can be a marker of tumor response to treatment. The far-red/near-infrared emission of Cy5.5 makes it suitable for in vivo imaging experiments where deeper penetration into tissues is needed. | price> |
R-C-5730 | PAA-PAN-PAM solid content 10% | Polyacrylic acid and polyacrylamide can be used to prepare polyacrylamide. Polyacrylamide has high water absorption and water retention properties, and is often used to prepare water absorbing and moisturizing materials such as hydrogels, hydrated adhesives, medical dressings, agricultural protectants, etc. | price> |
R-M2-9748 | BODIPY-Tetrazine | BODIPY-tetrazine is a fluorescent probe.BODIPY-tetrazine was used to fluorescently label DBCO-functionalized liposomes via strain-promoted inverse electron-demand Diels–Alder cycloaddition. | price> |
R-C-5731 | PS-r-PMMA-OH | PS-b-PMMA-OH,Random copolymers for substrate modification, but instead used hydroxyl(OH)end grafted PS-r-PMMA and identified surface neutrality through contact angle measurements.The use of the OH end group on the random copolymer allows the copolymer to end-graft itself to the silicon oxide layer of the substrate,and therefore immobilizes it. | price> |
R-M2-9749 | KLGFFKR-DOTA | KLGFFKR-DOTA/KLGFFKR-1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid/KLGFFKR,DOTA labed/DOTA-KLGFFKR is a peptide conjugate functionalized with a DOTA chelator for radiometal coordination, enabling targeted imaging or therapy. The peptide sequence KLGFFKR may facilitate targeting or cellular uptake, while DOTA allows stable complexation with diagnostic or therapeutic metal ions. | price> |
R-C-5732 | FFNPs | nanoscale zerovalent iron (Fe0-NPs) has gained prominence for environmental remediation,especially for the remediation of contaminants that are susceptible to reductive transformation such as azo dyes, especially,Agglomeration of magnetic metal nanoparticles takes place primarily through direct interparticle interactions. | price> |
R-M2-9750 | DSP-PEG4-TK-COOH | DSP-PEG4-TK-COOH is a ROS-responsive linker molecule designed for: Anchoring to hydrophobic surfaces (e.g., liposomes, nanoparticles) via DSP or DSPE. Controlled release via thioketal cleavage in oxidative environments. Conjugation to amine-containing drugs, peptides, or targeting ligands through the carboxylic acid end. DSP-PEG4-TK-COOH was incorporated into the liposomal membrane to enable ROS-sensitive release of surface-bound cargo via thioketal cleavage. The terminal carboxyl group was used to conjugate targeting ligands through EDC/NHS chemistry. | price> |
R-C-5733 | FA-PEG37-PDMAEMA40 | PDMAEMA-PEG-FA,FA-PEG-PDMAEMA,PDMAEMA possesses pH-responsive properties, as it becomes protonated and water-soluble under acidic conditions. It has been widely used in drug delivery systems and as a gene delivery vector due to its ability to encapsulate and release therapeutic molecules.The PDMAEMA-PEG-Folate conjugate can be used for targeted drug delivery, where the PDMAEMA segment can encapsulate therapeutic molecules and respond to the acidic environment in the tumor, leading to drug release. | price> |
R-M2-9751 | DMG-peg-CGEAIPMSIPPEVK | DMG-PEG-CGEAIPMSIPPEVK is a lipid–PEG–peptide conjugate designed for surface presentation of a bioactive or targeting peptide on lipid-based systems (e.g., liposomes, micelles). The DMG anchors the molecule into lipid bilayers, while PEG spaces the peptide outward, allowing biological interaction with targets such as receptors or enzymes. | price> |
R-C-5734 | Galactosylated chitosan(GC) | Galactosylated chitosan is a modified form of chitosan, a polysaccharide derived from the deacetylation of chitin, a natural polymer found in the shells of crustaceans.Galactosylation imparts Galactose receptors targeting properties to chitosan, which can selectively bind to the asialoglycoprotein receptor (ASGPR) found on the surface of hepatocytes in the liver. | price> |
R-M2-9752 | Chol-peg-CGEAIPMSIPPEVK | Chol-PEG-CGEAIPMSIPPEVK/Cholesterol-peg-CGEAIPMSIPPEVK is a surface-functionalized amphiphilic conjugate, designed for incorporation into lipid membranes. The cholesterol moiety anchors into lipid bilayers, the PEG linker provides spatial separation and mobility, and the peptide is displayed on the membrane surface for biological recognition, targeting, or signaling.Chol-PEG-CGEAIPMSIPPEVK was inserted into preformed liposomes to present the peptide sequence on the outer surface, facilitating targeted interaction with specific cellular receptors. | price> |
R-C-5735 | DSPE-PEG2K-N-acetyl-L-cysteine | DSPE-PEG-N-acetyl-L-cysteine,N-acetyl-L-cysteine(NAC) is a mucolytic agent with antibacterial and antibiofilm properties against several bacterial strains. it shows potential in inhibiting biofilm formation and even disrupting mature biofilms,that NAC acts on reducing the production of exopolysaccharides and leads to disruption and degradation of EPS matrix components. | price> |
R-M2-9753 | DMG-TK-PEG2K-CGEAIPMSIPPEVK | DMG-TK-PEG2K-CGEAIPMSIPPEVK is a lipid–ROS-cleavable–PEG–peptide conjugate, engineered for surface display of a bioactive peptide on lipid-based systems with ROS-triggered release capability. | price> |
R-C-5736 | MTX-PEI25k (Branched chain) | PEI-MTX,MTX-PEI,Polyethyleneimine(PEI)is a cationic polymer,it widely used as a gene delivery vector.PEI can complex with nucleic acids,protect them from degradation,and facilitate their intracellular delivery.Additionally,PEI possesses protonatable amino groups that enable endosomal escape, enhancing gene expression.MTX refers to methotrexate, a chemotherapy drug that inhibits the synthesis of nucleotides,leading to the suppression of DNA replication and cell proliferation.PEI-MTX conjugate combines the beneficial properties of both PEI and MTX for targeted drug delivery.The MTX moiety in the conjugate acts as a targeting ligand that can specifically bind to folate receptors,which are frequently overexpressed on the surface of cancer cells. | price> |
R-M2-9754 | N3-PEG1000-TK-NHS ester | N3-PEG1000-TK-NHS ester,Azido-PEG1000-TK-NHS ester is a bifunctional, ROS-cleavable linker.N3-PEG1000-TK-NHS ester,Azido-PEG1000-TK-NHS ester was used to conjugate a targeting peptide to DBCO-functionalized liposomes.The TK linker allowed ROS-sensitive release of the conjugated ligand in tumor-like oxidative conditions. | price> |
R-C-5737 | PEG2K-Se-Se-PEI20K | PEG-Se-Se-PEI,PEI-Se-Se-PEG,The disulfide bonds linking the PEI and Se atoms in the conjugate are sensitive to the intracellular environment,specifically the high levels of reductive agents such as glutathione.This sensitivity allows for the controlled release of the payload (e.g,genes or drugs) in the target cells.The reduction of the disulfide bonds leads to the detachment of the payload from the delivery system,facilitating its release and subsequent biological activity. | price> |
R-M2-9755 | COOH-CeO2 nanoparticles 3-5nm | Carboxyl-modified ceria nanoparticles(CeO2-COOH) were conjugated to amine-functionalized peptides via EDC/NHS coupling for targeted antioxidant delivery in oxidative stress models. | price> |
R-C-5738 | PCL5000-PEG2000-TTBZ | PCL-PEG-TTBZ,The carrier(PEG-PCL)has low cytotoxicity and forms micelles with a hydrophobic core and hydrophilic outer layer due to the amphiphilic block of PEG-PCL.This structure increases the water solubility of levodopa,improves its stability in circulation,provides targeted drug delivery,increases the local accumulation concentration of levodopa in dopamine neurons,thereby improving the bioavailability of the drug,enhancing its protective effect on neurological diseases such as Parkinsons disease,and reducing its peripheral toxic side effects. | price> |
R-M2-9756 | NH2-PEG2k-Se-Se-COOH | NH2-PEG2k-Se-Se-COOH/Amine-PEG2k-Se-Se-COOH could serve as a PEG-based linker for PROTAC (PErotein Degradation Tag) molecules.The structure could be used to modify nanoparticles, enhancing their stability, solubility, and surface properties. | price> |