JenKem proprietary Y-shape PEGs are more selective, due to their sterically bulky structure. The amine group is more reactive towards acylating agents than the hydroxyl group; readily undergoes reductive amination reactions.
JenKem proprietary Y-shape PEGs are more selective, due to their sterically bulky structure. The amine group is more reactive towards acylating agents than the hydroxyl group; readily undergoes reductive amination reactions.
Y-shaped Propion Aldehyde PEG. Reactive PEG for N-terminal amine in the presence of a reducing reagent; less selective but more reactive compared with Y-AALD-40K; reacts at pH 5-8. JenKem Technology's patented products, Y-shape PEG derivatives, also
Y-shaped Acetaldehyde PEG. N-terminal amine reactive PEG in the presence of a reducing reagent; less reactive but more selective compared to linear PEG aldehydes; reacts at pH 5-8. JenKem Technology's patented products, Y-shape PEG derivatives, also
Y-shape Maleimide PEG. Thiol reactive PEG ; reacts at pH 5.0-6.5. JenKem Technology's patented products, Y-shape PEG derivatives, also known as branched PEG derivatives, contain two linear methoxy PEG chains attached to a central active core. JenKem
Y-shape PEG NHS from JenKem Technology is a Succinimidyl Carboxymethyl Ester with two PEG arms, reactive towards the amino group of lysine(s) on proteins or other biologics. Amine PEGylation with Y-shape PEG NHS can be completed in less than 1hr at p
Y-shaped Carboxyl PEG suitable for amine PEGylation. JenKem Technology's patented products, Y-shape PEG derivatives, also known as branched PEG derivatives, contain two linear methoxy PEG chains attached to a central active core. JenKem proprietary Y