
Should you require a product that is not listed or believe your needs are not covered here, please do not hesitate to contact us, we will do our best to match your research requirements at a very affordable price.
Standard synthesis scales
The table below describes our classical, most frequently requested syntheses. We routinely prepare higher amounts (up to several grams) and longer peptides. Please contact us with your sequence(s), amount and purity level and we will always respond with a very competitive offer.
|
Standard Purity levels / Amounts: |
> 99% | 2-5 mg |
| > 95% | 5-10 mg | |
| > 80% | 10-15 mg | |
| > 70% | 20-25 mg | |
| Analytical Data : | HPLC trace (220 nm) & Mass Spectrum (MALDI-TOF) | |
| Peptide Length : | Up to 30 aa | |
| Structure : | Unblocked termini (i.e. NH2- and-COOH ends) | |
Reverse phase HPLC purification
HPLC purification options include guaranteed purities >70%, >80%, >95% and a unique ultra-pure >99% grade for demanding experiments.
Purification is performed by preparative or semi-preparative reversed-phase HPLC. We typically use C8 or C18 columns with linear gradients of acetonitrile in 0.1% aqueous tfa with UV monitoring at 220 nm.
HPLC elution may be monitored with UV detector set at longer wavelength for peptides containing aromatic amino acids.
The crude peptide synthesis contains by-products resulting from failed coupling cycles (i.e. truncated chains), and further oxidation, modification, or hydrolysis of side chains arising during cleavage and deprotection. The extent of impurities depends upon peptide length and primary sequence. Depending upon your specific application we would recommend purification levels along the following guidelines.
Quality control
We recognize that quality and reliability are central to our customers. As a result no peptide leaves our laboratories unless it has fully complied with our stringent QC standards.

- Fig 2. Reverse phase HPLC analysis of a 10-aa peptide containing two aromatic residues (tyr) with dual wavelength recording: 220 nm and 280 nm. Co-elution of both absorptions confirms product purity. C8 column 4.6x250mm, 5μm. Gradient 15-50% acetonitrile in 0.1% aqueous tfa in 25 min, flow rate 1ml/min.
- Click on figure to enlarge
Fast reliable peptide delivery
All our peptides are weighted and supplied as a stable lyophilized powder with comprehensive documentation. Synthesis report includes analytical HPLC trace verifying purity and a mass spectrum ensuring integrity of the desired full-length peptide. Dispatch time will vary with length, scale, purity, and modifications ordered. Our average turn around is shown in the table below, for standard synthesis scales and purities. Our customers are well advised when synthesis difficulties are encountered and product is delayed.
| Synthesis | 25 mg, >70% | 15 mg, >80% | 10 mg, >95% | 5 mg, >99% |
| Average (*) | 2 weeks | 2 - 3 weeks | 3 weeks | 3 - 4 weeks |
Long chain peptides
We routinely prepare long (30-50 aa) to very long peptides up to a maximum length of approximately 100 aa. Because overall yield decreases exponentially with increasing length, synthesis and downstream processing times may increase significantly for longer sequences.
Many peptides of length over 40 aa have raised important research interest and their syntheses remains challenging. We have been manufacturing peptides > 40 aa with consistent high potency biological activity for many years.
This unique peptide grade includes an additional purification step following standard reversed-phase HPLC elution. It was developed by Genosphere Biotechnologies in collaboration with several research groups using our peptides in cell culture assays. It has been tested with a large number of cell types and exhibits no detectable cytotoxicity commonly associated with standard peptides at higher concentrations.
It has also proven to yield peptides with high activity in sensitive biochemical assays. Another noteworthy feature is a considerably increased stability of the peptides in aqueous solutions.
Cyclic peptides have drawn considerable interest because of their improved chemical stability and significantly enhanced resistance to in situ enzymatic clearance. The conformation is more rigid then the open-chain analog and may explain in part some of the observed improved biological activities. We routinely prepare cyclic peptides with head to tail ring closure. Directed cys-cys disulfide cyclization (up to 2 per molecule) is also frequently achieved, and careful monitoring of the reaction ensures 100% cyclization.

- Fig 6. (b) N-terminal amine to internal glutamic acid cyclization of a 27 aa peptide containing 21 hydrophobic residue (theoretical molar mass 2894) was prepared (100 mg) with purity level >95% and a sample analyzed by MALDI-TOF MS. MS shows loss of H2O (-18 amu) by condensation to yield desired product with molecular ion at m/z 2895.0.
- Click on figure to enlarge
Depending upon your application we may prepare biotinylated or fluorescent peptides with various spacers. Aliphatic C3, C6 (ahx), C12, C18 or hydrophilic polyethylene glycol (PEG)-derived spacers are available.
Peptide ends
Our peptides are normally synthesized with unblocked termini i.e. amine and carboxylic acid groups.
However in some instances, one might consider using blocking moieties, or modified ends.
N-acetyl and C-amide closely mimic internal sequences as they have uncharged ends. In addition, these blocking groups improve resistance to enzymatic degradation.
| N-terminal (default NH2) | C-terminal (default COOH) |
| acetyl, formyl | amide |
| myristoyl | hydroxyl |
| carboxyl | thioester |
| 2-furoyl | (…) |
Many modifications available
Genosphere Biotechnologies provides a wide range of established peptide modification as detailed below.
| Unusual Amino acids | Chemical Modifications |
| D-enantiomers | Phosphorylation: Tyr, Ser, Thr |
| Hydroxyproline | Haptens: Biotin, DNP |
| Pyroglutamine | Anilide C-terminal |
| Methyl-, acetyl-lys | Benzyloxycarbonylation |
| 4-Bromo-, 4-Nitro-phe | Nitrosation |
| ß-alanine | N-Methylation |
| Fluorescent labeling | Macromolecular Conjugation |
| Coumarins (MCA, AMC) | Fatty acids: Palmitoyl-, steroyl-, |
| Fluorescein | Proteins |
| Rhodamine | Cyclization |
| DANSYL | Cys-cys disulfide bridge |
| NBD | Head to tail cycle |
| DABCYL | Lactam, internal |
A peptide is usually too small to elicit a satisfactory immune response in animals. In order to improve immunogenicity, one needs to attach the target peptide to a larger macromolecular structure. While protein carrier conjugation remains the preferred approach, the MAP (multiple antigen peptide) is used in some instances.
Protein carrier conjugation for immunization
Peptide epitopes are covalently conjugated to a larger carrier protein and the latter conjugate is used as immunogen to generate antisera.
Standard carrier is (Keyhole Limpet Hemocyanin-KLH), however other proteins are available for conjugation (Bovine Serum Albumin- BSA, Ovalbumin-OVA, etc.).
Deliverables: 5 to 10 mg of free peptide with requested purity level and 10-15 mg of peptide conjugate.
Multiple antigen peptides
Multiple antigen peptides (MAP) immunogens contains 8 copies (or 16 copies) of the peptide, synthesized directly on an 8-armed (or 16-armed) branched lysine core. The resulting multimeric is a large macromolecule (10-15 kDa) which has a high molar ratio of peptide antigen to core molecule and does not require further conjugation to a carrier protein. We typically prepare 10-20 mg of these peptides. Please note that MAP should not be used when the peptide sequence is derived from the C-terminus of the target protein.
We offer custom peptide librairies synthesis in 96-wells microplate formats. Whether you intend to screen peptides for enzyme substrate profiling, elucidate substrate specificities, protein-protein interaction region mapping, antibody epitope mapping, we provide cost-effective fmoc-based simultaneous multi-peptide synthesis technologiesto fit your needs.
Specifications
Peptide length : 5-18 aa
Free C-& N- termini unbound peptides
Amount: 1 mg (depends on sequence)
Purity: Screening / Crude grade (average purity 12mer>70%)
Analysis: Mass spectrum for every peptide
Turnaround: average 2-3 weeks
Pricing and quotation
All sequences are subject to technical evaluation and are quoted individually.
You may use our Online Quotation Form
Or if you wish to e-mail or fax, please indicate sequences (N to C terminus), mg amount, purity level, and modifications required.
Product delivery
All peptides are lyophilized, weighted and shipped by express courier at RT with a complete synthesis report that includes, an analytical reversed-phase HPLC trace (UV detection at 220 nm).
Ordering
An Online Order Form is available for your convenience. You may order by fax or e-mail as well.
For administrative purposes, we do require a copy (EMAIL/PDF, FAX or POST) of your institutional purchase order in all cases.
Please write sequences N to C termini and kindly use one-letter code designation of amino acids for quotation requests and orders.
| Alanine | ala | A | Leucine | leu | L |
| Arginine | arg | R | Lysine | lys | K |
| Aspargine | asn | N | Methionine | met | M |
| Aspartic acid | asp | D | Phenylalanine | phe | F |
| Cysteine | cys | C | Proline | pro | P |
| Glutamic acid | glu | E | Serine | ser | S |
| Glutamine | gln | Q | Threonine | thr | T |
| Glycine | gly | G | Tryptophan | trp | W |
| Histidine | his | H | Tyrosine | tyr | Y |
| Isoleucine | ile | I | Valine | val | V |



















