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Triazolylphenylglyoxal Reagents: Bioconjugation
Chemical ligation modifies biological macromolecules for biotech and medicine, expanding functional material development.
What is Click Chemistry? An Introduction
Explore click chemistry: efficient, high-yield reactions for drug discovery, bioconjugation, and green chemistry with simple conditions and wide applications.
Click Chemistry in Drug Discovery
Explore the principles and applications of click chemistry in drug discovery, highlighting efficient reactions that streamline the synthesis of bioactive compounds.
Click Chemistry in Drug Discovery
Explore the principles and applications of click chemistry in drug discovery, highlighting efficient reactions that streamline the synthesis of bioactive compounds.
Copper-Free Click Chemistry
Copper-free click chemistry is an alternative approach to click chemistry that proceeds at a lower activation barrier and is free of cytotoxic transition metal catalysts.
Crosslinkers Selection Guide
Choosing the right crosslinker for your biochemical or bioconjugation research can be challenging. Our selection guide can help you find the perfect match for your applications.
GlycoProfile™ Azido Sugars
GlycoProfile™ Azido Sugar portfolio offers peracetylated azido sugars for glycan structure modification via chemical or biosynthetic pathways.
Guanylation of Amines
Introduce guanidinyl group using guanylating reagents like bis(tert-butoxycarbonyl)thiopseudourea, polymer-bound, from substituted amines.
Polybrene® Technical Bulletin
Polybrene® neutralizes red blood cell charge, a vital anti-heparin agent in various laboratory applications.
Staudinger Ligation
Azides react with triarylphosphines to form iminophophoranes, a chemoselective synthetic method known as Staudinger Ligation.
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