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Custom Peptide Synthesis
Common peptide synthesis strategy is solid phase synthesis, which sequence generally synthesized from the N-terminus (amino terminus) to the C-terminus (carboxy terminus). In the past, peptide synthesis is carried out in solution so it is called liquid phase synthesis. Since Merrifield developed the solid phase synthesis method of peptide in 1963, it has been improved and perfected continuously. Today, the solid phase synthesis method has become a kind of common technique in the synthesis of peptides and proteins, showing the advantages unmatched by classical liquid phase synthesis, thus reducing the difficulty of purification of each step of the product greatly.
MHC tetramer is a complex of 4 MHC molecules associated with loaded peptide, which is bound to a fluorescently labeled streptavidin molecule. Monomeric MHC molecule is loaded with its cognate peptide, and biotin is linked to the complex at a site far removed from the T-cell recognition site.
PNAs, or peptide nucleic acids, is an analogue of oligonucleotide in which sugar-phosphate backbone has been replaced by a polyamide chain. Due to the unique backbone of PNA, it can be used in same applications as conventional DNA/RNA.
Recombinant expression of peptides offers a better alternative process to synthetically generate or isolated from natural sources. It produced relatively better quality peptides (in terms of purity) than chemical process, initial cost and time required for the development of recombinant process is higher than chemical process.
Peptoids are a bioinspired material whose properties lie in between natural biopolymers and nonnatural synthetic polymers. Like biopolymers, they are information-rich polymers, offering precise control of main chain length, side chain, functionality, and monomer sequence.
Stapled peptides have been shown safe, efficacious, and biological pathway specific in animal models of human cancer driven by Bcl-2 overexpression and constitutive activation of the NOTCH transcriptional activation pathway.
The overlapping peptide library is most commonly used for linear, continuous epitope mapping, where the aim is to generate a library of overlapping peptide sequences of specific length and specific offset, to cover the entire native protein sequence.
Long synthetic peptides (LSPs) have a variety of important clinical uses as synthetic vaccines and drugs. It often used for structural analysis by electron paramagnetic resonance, x-ray crystallography, and NMR or are immobilized as bait in affinity chromatography. Therefore, quantity and purity requirements for LSPs are high.
Large-scale quantities of peptides (>1g) are practical for use as biological additives in healthcare products or therapeutics containing synthetic peptides.
We have been producing synthetic oligopeptides for many years. Our experience and manufacturing capabilities in oligopeptide synthesis manufacturing allows us to produce the highest quality, large-scale oligopeptides with a high success rate.
Creative Peptides provides high-quality, low-cost, high-tech peptide products to customers around the world. The company's products have been successfully sold to pharmaceutical companies including Europe, North America, Asia and Oceania. Every step of peptide synthesis is subject to Creative Peptides’ stringent quality control. Typical delivery specifications include:
- HPLC chromatogram
- Mass spec analysis
- Synthesis report
- Certificate of Analyses
 Rogers, J. M., & Suga, H. (2018). Molecular Technologies for Pseudo-natural Peptide Synthesis and Discovery of Bioactive Compounds Against Undruggable Targets. Molecular Technology: Life Innovation.
 Gundluru, M. (2018). Custom Synthesis of Strained Cyclooctyne-Peptide Conjugates for Copper-Free Click Chemistry. Peptides International, Inc.: Louisville, KY, USA.
 Benoiton, N. L. (2016). Chemistry of peptide synthesis. CRC Press.