News

Visit this regularly updated section to check out the latest additions to our portfolio, as well as the latest developments at Iris Biotech.

  1. MiDye550-Alkyne

    Properties of the MiDye Chromophore System:

    • Readily applicable to biolabelling, Click 
      conjugation protocols and peptide synthesis
    • Stable under buffer conditions (pH 4-8) 
      and in solid phase peptide synthesis
    • Broadly applied in cell und animal 
      imaging, tested in FRET systems
    • Available in larger quantities compared 
      to e.g. Alexa, Cy-Dyes etc.
    • Purities > 85%, supplied as freeze-dried solid powder

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  2. Available Bulk

    Our portfolio currently contains over 5500 products. Many of them – in particular standard consumables for peptide synthesis – are being produced in bulk quantities.  Therefore we can keep our prices also for lab quantities at very competitive level.

    In case of need for bulk quantities please inquire:

    - All 20 Proteinogenic Fmoc-protected Amino Acids are available in 100+ kg Lots;

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  3. Alpha-Sulfo-beta-Alanine

    alpha-Sulfo-beta-Alanine has been used to couple to hydrophobic labels like Cyanine and Rhodamine dyes and other hydrophobic residues to increase their solubility in water. As di- or tripeptide a further increase of hydrophilicity can be achieved. Fmoc-beta-Ala(SO3H)-OH can be coupled in SPPS by standard phosphonium or uronium based coupling reagents. In high throughput technologies for DNA sequencing and genomics charge-modified dye-labeled dideoxynucleoside-5’-triphosphates were synthesized for ‘direct-load’ applications in DNA sequencing.

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  4. Cross-Linker: Mal-AMCHC-OSu

    Mal-AMCHC-OSu

    trans-N-Succinimidyl 4-(maleimidomethyl)cyclohexane-1-carboxylate

    Formula:                    C16H18N2O6
    Molecular Weight:     334,33 g/mole

    CAS:  64987-85-5

    CODE:  MAA1000

    1g:       EUR    300,-    US$   420,-
    5g:       EUR  1200,-    US$ 1680,-

    Prices are in EUR, net, exw Germany, shipping not include

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  5. Troc-OSu

    Reported applications:

    Introduction of 9-fluorenylmethyloxycarbonyl, trichloroethoxycarbonyl, and benzyloxycarbonyl amine protecting groups into O-unprotected hydroxylamino acids using succinimidyl carbonates; Anelka Paquet; Can. J. Chem.; 1982; 60: 976.

    Widely Applicable Deprotection Method of 2,2,2-Trichloroethoxycarbonyl (Troc) Group Using Tetrabutylammonium Fluoride; Cheng-yuan Huanga; Ning Wanga; Katsumasa Fujikia; Yuji Otsukaa; Masao Akamatsua; Yukari Fujimotoa; Koichi Fukasea; Journal of Carbohydrate Chemistry 2010; 29(6): 289 – 298.

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  6. DTT (Cleland's Reagent)

    Cleland's reagent, also known as dithiothreitol or DTT is a water soluble protective reagent for sulfhydryl groups.
    It reduces disulfide linkages to free sulfhydryl groups in proteins and enzymes.
    It is a component of buffers used in protocols for the isolation and purification of proteins.

    DTT (racemic), Cleland's Reagent

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  7. Actiplus-CALB

    Lipase B from Candida antarctica (EC 3.1.1.3)
    adsorbed on hydrophobic polymer Polystyrene DVB cross linked, 300-700µm,
    Synthetic Activity >10.000 U/g (dry), 
    very high mechanical stability - suitable for packed bed reactors

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  8. Green Advantages of using Phacm for Cystein Protection

    PGA (Penicillin G Amidase, Penicillin Acylase, Penicillin Amidohydrolase from E.coli on acrylic resin, Systematic name: Penicillin amidohydrolase, E.C. 3.5.1.11) has an active pocket, which is very specific for phenyl acetic acid. The prominent commercial use is hydrolysis of a phenylacetamid bond during production of the penicillin API 6-APA (De Martin et al., J. Mol. Catal. B:Enzymatic 1999; 6: 437). The high specifity of PGA towards the Phenylacetyl moiety makes the use of Phacm as new alternative for Acm very promising. The principle use already was discovered by Albericio et al in 1995 using native PGA. Today PGA is available as immobilized preparation, so by simple filtration process PGA can be removed from the reaction mixture and reused many times.

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  9. Dendron Building Blocks for Click Chemistry

    Dendrimers offer a new possibility to derivatize small molecules, surfaces or biopharmaceuticals with a monodisperse macromolecule and alter in this way properties like solubility and hydrophilicity. Immunogenicity and pharmacokinetics of pharmaceuticals will be improved. The synthetic approach for designing these dendrons of different generations is based on 2,2-bis(hydroxymethyl) propionic acid, which is a non-toxic and biocompatible building block.

    The size can be designed from 250 g/mole for 1st generation dendrons to over 4400 g/mole with 5th generation compounds. Dendrimers can be designed reaching even a molecular weight of some 10.000 Da. As focal point alkyne and azido functions are used with appropriate counter parts in any type of click chemistry reaction. Olefinic functions offer the possibility for addition reaction or conjugation by metathesis reactions or photo reactions with the aid of UV light. For the modification of Gold surfaces sulphur bearing dendrons can be used, they also conjugate with biologicals via disulfide bridge formation.

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