LNA Building blocks improve duplex stability and binding specificity of oligos by locking the sugar backbone into a rigid 3'-endo envelope conformation. Explore their unique advantages!
Recent years have seen major advances in greener peptide synthesis. To highlight such products, we introduced the category "Green Chemistry" on our website.
The 2'-position of the ribose sugar wears many hats: enhancing stability, extending half-life, and boosting target binding of DNA/RNA. Discover available modifications & explore their benefits!
Building on our peptide chemistry expertise, we set sail into new waters, offering nucleic acid building blocks for oligonucleotide synthesis to expand innovation across biomolecular research.
Anchor your peptides: Unlock the secrets of defying protease attacks and extend the serum half-life of your next peptide medication. Our building blocks will help you to reach your goals.
From fragments to full peptides - ligases like e.g., Sortase, Omniligase, enable efficient ligation and cyclization. Read our blog and learn how enzymatic tools can enhance your peptide synthesis.
A photolabile anchor for SPPS that facilitates the synthesis of thioesters for native chemical ligation and which can be used to generate peptide chains fragmenting by flash photolysis. To discover NIC, read on!
New azidobenzyl side-chain-protected aspartic and glutamic acid building blocks allowing, e.g., for selective reductive deprotection even in physiological systems.
The example of Semaglutide: Improve the pharmacokinetics of your therapeutic peptides by increasing their resistance against proteases via binding to plasma proteins.
We say "UAA"! By genetic code expansion you can incorporate our novel aminocoumarinyl lysine in your favorite protein where it serves you as fluorescent probe or photo-activatable caged lysine.