Results for Lipids & Polymers ( 10111 )
benzyl N-[2-(prop-2-enamido)ethyl]carbamate is a short aliphatic linker featuring a Cbz-protected amine and an acrylamide. Acrylamide is a Michael acceptor which is a good Michael acceptor which can be used in thiol-based bioconjugation or polymerization. Meanwhile, the Cbz protecting group can be removed using Pd-C hydrogenation to reveal a free amine that can participate in a wide variety of reactions such as couplings or reductive amination.
- Ref: BP-40202Sizes: 1 G, 100 MG, 500 MG, 250 MG
- Ref: BP-40203Sizes: 100 MG, 50 MG, 500 MG, 250 MG
16-(Bromoacetamido-PEG6-ethylcarbamoyl)pentadecanoic-t-butyl ester is a PEG linker featuring a bromoacetamide and a terminal t-butyl ester. Bromoacetamide is a thiol-specific covalent ligand which can be used in labeling proteins via their cysteine residues, while the t-butyl ester can be hydrolyzed to reveal a carboxylic acid that can be used to couple with amines or alcohols.
DOPE-PEG-FITC, MW 5,000 is a PEG-lipid that features a DOPE phospholipid and an FITC fluorophore. DOPE is an unsaturated phospholipid that is commonly used to prepare lipid nanoparticles in drug delivery, while FITC is a green fluorophore with excitation and emission maxima at 491 nm and 516 nm respectively. FITC-PEG conjugates see frequent use in fluorescence microscopy, immunohistochemistry and other in vivo research applications.
N-(Acid-PEG8)-N-bis(PEG8-Azide) is a trifunctional molecule that combines two azide functions with a carboxylic acid via a tertiary amine at its center. The azides can be reacted with terminal alkynes or cyclooctynes to form stable triazoles with a target molecule. Meanwhile, the carboxylic acid can be coupled with amines using reagents such as HATU or EDC.
DSPE-PEG-DBCO, MW 2,000 is a PEG lipid conjugate featuring a DSPE phospholipid and a DBCO group. DSPE is a saturated phospholipid that is commonly used to prepare lipid nanoparticles in drug delivery, while DBCO is a click chemistry handle that is frequently used to conjugate with azides on target molecules to form stable triazole linkages.