Explore RGD peptides, key integrin receptor inhibitors used as tumour homing peptides, and for the functionalisation of inert biomaterial to promote cell adhesion in tissue engineering and 3D cell culture applications.
Learn more about PEGylated peptides, how they outperform unmodified peptides, and their impact on modern drug development.
Explore key considerations for designing fluorescent peptides, including dye selection, spacers, handling, and storage. Read our guide.
From medicines and diagnostics to skincare and agriculture, peptides are everywhere. Discover how these tiny molecules have such a big impact.
Peptide synthesis is a cornerstone of modern science, underpinning advances in medicine, biotechnology, and fundamental research that enable the creation of molecules that drive advancements in medicine, research, and technology.
Why are cyclic peptide therapeutics gaining momentum in drug discovery? Learn how they compare to linear peptides and other drug modalities plus view a recent example of protein-protein interaction inhibitor that we have recently synthesised.
Peptide cyclisation is a useful modification employed to enhance the properties of linear peptides. Discover four methods to cyclise peptides.
What are cyclic peptides? In this latest article, we explore examples, their synthesis and applications. Click to learn more.
Peptide conjugation to oligos, biotin, dyes, tags, proteins or other molecules, is a strategy to expand their utility in various fields. Discover our capabilities in this latest article.
Fmoc solid phase peptide synthesis (SPPS) is the method of choice for peptide synthesis. Compared to the traditional Boc/Benzyl approach, Fmoc chemistry is a convenient and milder method for the manufacture of peptides.