Peptide Chemistry

We have a substantial, long-standing expertise in peptide synthesis, providing tailored peptides with highest quality for even complex or unusual peptide sequences. Our highly skilled and committed scientific staff ensures that the most appropriate modifications, purities, methods, peptide synthesizers and techniques are selected for every custom peptide synthesis project.

Most of JPT's specialty peptides are provided in the highest purity (>95%), with a full range of peptide analyses including LC-MS (trap and/or quad), MALDI-MS or HPLC. A large variety of optional analyses is available e.g. AAA, NMR, CE, sterility testing, as well as peptide content determination.

The exceptional quality and reliability of our peptide synthesis service has been appreciated by customers worldwide for many years.

Selection of common peptide modifications and labeling options.

For a detailed description of the different options and a full list,
please visit our Specialty Peptide Synthesis page

Fluorescence and chromogenic labeled peptides (FITC, Carboxyfluorescein, Alexa, AMC, FRET peptides, etc.)

  • Peptide esters
  • Internally quenched peptides (FRET peptides: Abz/nitroTyr, EDANS/DABCYL, MCA/DNP labeling) guaranteed without fluorescent impurities
  • Immunogenic peptides (MAPs, palmitinylation, Pam3Cys labeling, etc.)
  • Phosphopeptides (phosphorylated tyrosine, threonine or serine) and peptidomimetics (amide bond isosteres, non-natural amino acids, etc.)
  • Post-translational modifications (PTMs) such as acetylation, methylation, phosphorylation, citrullination e.g. acetyl lysine and acetyl arginine peptides, methyl lysine and methyl arginine, citrullin, lysine succinyl, butyryl, propyl... etc.
  • Non-commercial building blocks for custom peptide synthesis
  • Biotinylated peptides (N-terminal and C-terminal biotinylation as well as biotin attached via side chains – via special optimized linker / spacer)
  • D amino acid peptides (D peptides)
  • Labeled custom peptides (stable isotope labeling (heavy peptides), chromophore, etc.)
  • Cyclic peptides (disulfide bridges, lactams, thioether-bridges, etc.)
  • Long peptides (>70 amino acids)
  • Site-directed conjugations of custom peptides with KLH, BSA, ovalbumine or other carriers

    Please inquire about additional peptide modifications not listed here

Selected References for custom peptides:

“Methods to Measure MDSC Immune Suppressive Activity In Vitro and In Vivo”
Samantha Solito et al., Current Protocols in Protein Science (2018) - PMID: 30303619
“A Versatile T cell-based Assay to Assess Therapeutic Antigen-specific PD-1-Targeted Approaches”
Versteven et al., Oncotarget (2018) - PMID: 29963238
“Decoy Peptides Derived from the Extracellular Domain of Toll-like receptor 2 (TLR2) show Anti-inflammatory Properties”
Versteven et al., Bioorganic & Medicinal Chemistry (2018) - PMID: 29963238
“Method For Inducing Oral Tolerance Via Administration of Beta-Lactoglobulin Derived Peptides in Combination With Probiotic”
Knippels et al., US Patent App. 15/558,669 (2018) - PMID: n.a. 
“T‐cell tracking Using Cerenkov and Radioluminescence Imaging”
Boschi et al., Journal of biophotonics (2018) - PMID: 29770603
“Platelet Characteristics in Patients with Essential Thrombocytosis”
Pedersen et al., Cytometry Part B: Clinical Cytometry (2018) - PMID: 29790256
“Platelet Subpopulations Rremain Despite Strong Dual Agonist Stimulation and can be Characterised Using a Novel Six-Colour Flow Cytometry Protocol”
Södergren et al., Scientific Reports (2018) - PMID: 29362366

More references

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Contact: Tanja Kaan
T: +49-30-6392-7878
X: +49-30-6392-7888

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