Blog | Page 45

  1. PEG-Conjugates of Folic Acid and Cholesterol

    Conjugates of PEG and folic acid or cholesterol, respectively, combine the positive properties of these molecules. Those conjugates are available with a wide variety of functional groups and different PEG chain lengths to suit your needs.

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  2. Triamino Acids

    Fmoc-L-Dap(2-Boc-aminoethyl)-OH is the first in a series of new triamino acid building blocks. This azalysine is useful for introducing positive charges into a peptide, or for creating branched structures.

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  3. The 7th World ADC Conference

    10-13 October 2016
    San Diego, CA, USA
    Marriot Marquis & Marina

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  4. Thailand LAB International 2016

    21-23 September 2016
    Bangkok International Trade & Exhibition Centre (BITEC)
    88th Bangna Trad Road, Bang Na, Bangkok 10260, Thailand

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  5. CPhI worldwide

    4-6 October 2016
    Fira de Barcelona Gran Via, Barcelona
    Spain

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  6. Photocleavable NCL-Auxiliary Glycine

    This innovative auxiliary facilitates Native Chemical Ligation at the position of a Glycine residue in a peptide sequence. The auxiliary can be further functionalized, e.g. by PEGylation. Following NCL, the auxiliary is removed by irradiation with UV light.

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  7. Building Blocks for the SPPS of FRET-based fluorogenic protease substrates

    The classic FRET pair EDANS and DABCYL is now available linked to Fmoc amino acid building blocks that can be readily used in SPPS. Conveniently synthesize your own custom protease substrates!

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  8. 34th European Peptide Symposium

    September 4th - 9th, 2016
    University Campus Augustusplatz Leipzig
    Germany

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  9. Omniligase-1 for Efficient Peptide Ligation

    Omniligase-1 enables efficient and racemization-free ligation of two side-chain unprotected peptide fragments at many different positions. Test this innovative enzyme developed by EnzyPep B.V. using the complementary model peptides included in our kit!

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  10. The Safety-Catch Acid-Labile (SCAL)-Linker

    The SCAL linker offers superior chemical stability and permits a variety of orthogonal solid-phase approaches. It is fully compatible with the Fmoc-, Boc- and Alloc- strategies. Cleavage can be performed either by a simultaneous, or by a two-step reduction/acidolysis procedure to afford peptide amides.

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