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Intavis Peptides

INTAVIS peptide services

This website offers you as our customer detailed information about the portfolio of our business division INTAVIS peptide services. You have the possibility to order online custom peptides as well as custom peptide arrays and resins for peptide synthesis from our labs in Heidelberg and Reutlingen tailored to your particular needs.
Custom peptides are a useful tool for a wide variety of experimental approaches. Ranging from the use of purified custom peptides for quantitative studies to peptide libraries and CelluSpots™ peptide arrays for screening purposes of epitopes or kinase specifity, INTAVIS peptide service offer resins for solid phase peptide synthesis.

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Peptide Team at ACS Meeting

Meet our Team at the ACS Spring Meeting in San Diego

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Peptide Services of INTAVIS AG Reutlingen has moved

New phone and fax number for contact Reutlingen.

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Frequently Asked Questions

How are the peptides synthesized?
Fmoc chemistry is used to synthesize the peptides on a solid support from the C-terminus to the N-terminus of the sequence.

What are the right C- and N-terminal endings of the peptides?
This depends on the application you have in mind for your peptides. It may be a good idea to choose the terminal ends of the peptide dependent on the natural occurrence of the sequence: 1. The peptide(s) should mimic an internal sequence of a protein. The peptide(s) should not be charged at the ends. The N-terminus of the peptide(s) should be acetylated and the C-terminus should be an amide. 2. The peptide sequence is the C-terminal end of a protein. The C-terminus should be the free acid and the N-terminus should be acetylated. 3. The peptide sequence is the N-terminal end of a protein. The C-terminus should be an amide and the N-terminus should be in the natural free amine form. • For cytotoxic T-cell epitope studies the peptides should have both, a free amino group at the N-terminus and a free acid at the C-terminus. These ends are the natural equivalents to the peptide fragments, processed intracellularly from whole proteins. • Peptides with acetylated N-terminus and an amide as C-terminus are more resistant to exopeptidases, which may be an important factor regarding the time a peptide will be functional in a biological assay. • Biotinylated peptides can be useful in combination with streptavidin coated surfaces (e.g. beads, plates or microarrays). • Peptides with a thiole group (e.g. cysteine) can be directly bound to gold surfaces or to amino groups by the use of bifunctional crosslinkers.

How are the peptides supplied?
The peptides are delivered lyophilized. Ambient temperature should not be a problem for the lyophilized peptides. However, for maximum stability the peptides should be stored at -20°C.

How do I store my peptides?
The lyophilized peptides should be kept in a cool, dark place. Long term storage of the peptides should be done in a freezer at -20 to -80°C. Most peptides stored in this way will remain stable for several years. Peptides in solution are not as stable as in the lyophilized form. Peptide solutions should be neutral to slightly acidic (pH 5-7) and stored frozen at -20°C. To avoid repeated freeze-thaw cycles it is recommended to divide the stock solution into aliquots. • maintain sterile conditions • Cys, Met and Trp residues tend to oxidize (oxidation-rate increases with pH)

How do I solubilize my peptide(s)?
The solubility of peptides is strongly dependent upon the peptide sequence. For some very hydrophobic sequences it may not be possible to use aqueous solutions without any additional organic solvents. 1. Try to dissolve the peptides in sterile water with sonication (1-10 mg peptide/ml). 2. If this fails, add acetic acid up to a total concentration of 10% (v/v) for basic peptides or aqueous ammonia for acidic peptides and sonicate. (Count the number of basic (R, H, K and free N-terminus) and acidic residues (D, E and free C-terminus) of the peptide) Examples: Ac-HN-RFREQIVKPFK-CONH2 -> 0-1+0-1+1+0+0+0-1+0+0-1+0 = -3 -> basic peptide H2N-FVQADIDYIT-COOH -> -1+0+0+0+0+1+0+1+0+0+0+1 = +2 -> acidic peptide 3. For peptides that remained insoluble add organic solvents such as acetonitrile, DMSO or DMF up to a concentration of 20% (v/v). NOTE: The use of organics such as acetonitrile, DMF, DMSO etc. may interfere with some biological assays. If DMSO is used, peptides with Cys, Met and Trp oxidize faster!

My peptide has a purity of 95% - what are the other 5%?
The peptide purity gives the percentage of the correct sequence in a given sample. The rest of the sample consists of truncated sequences, deletion sequences or otherwise modified sequences.

What is the net peptide content of my peptide(s)?
The weight of the lyophilized peptide composes of the peptide and water weight. The water and counter-ion content vary widely, depending on the given peptide sequence. Typically 90% are peptide and the other 10% are water and counter-ions. For some highly charged peptides the water and counter-ion content can increase up to 30%.

What is the length of the peptides you can synthesize?
The minimum length of peptides should not be less than 5 amino acids. For shorter peptide sequences cleavage from the synthesis resin and following purification can cause problems. The standard maximum lengths are peptides with up to 40 residues. However, upon request we will synthesize longer peptides (>60 amino acids).