Lipids & Polymers

Bead-conjugated antibody pair compatible with Simoa® (single molecule array) and similar assays for detecting rat NF-L in various sample types. The kit includes a bottle of capture beads, a bottle of detection reagent and standards.

Poly(DL-lactide) (PDLLA) is an ubiquitous biodegradable polymer. It is typically used to fabricate medical devices that predictably degrade over months in physiological conditions. The well-researched release profile also allows for drug-release functionalization with calculable results. Owing to its extensive history, PDLLA is one of the most understood and affordable biodegradable polymers for medical devices today.

MPEG-2000-DSPE sodium is a phospholipid PEG conjugate with hydrophilicity and hydrophobicity. It is utilized in liposome synthesis to enhance the hydrophilicity of liposomes, thereby prolonging their circulation in the bloodstream. This compound is commonly employed for the investigation of anticancer and antimalarial agents.

Azido-PEG3-C6-Cl is a PEG-based linker for PROTACs, which connects two essential ligands crucial for PROTAC molecule formation, enabling selective protein degradation via the ubiquitin-proteasome system within cells.

Pomalidomide-PEG6-NH2 hydrochloride is a compound resulting from the synthesis of an E3 ligase ligand-linker conjugate, combining the cereblon ligand derived from Pomalidomide with a 6-unit PEG linker, specifically designed for application in PROTAC technology.

Thalidomide-PEG4-NH2 hydrochloride is an E3 ligase ligand-linker conjugate compound, comprising the cereblon ligand from Thalidomide and a linker specifically used in PROTAC technology.

A 410099.1 amide-PEG2-amine-Boc is a functionalized IAP ligand for PROTACs, combining an IAP ligand with an amide-PEG3 linker terminating in an amine, facilitating the formation of conjugates with target protein ligands.

A 410099.1 amide-PEG3-amine-Boc is an IAP ligand-based functionalized molecule commonly used in PROTACs, consisting of an IAP ligand and an amide-PEG3 linker with a terminal amine. The compound effectively conjugates with target protein ligands.