MAL-dPEG®₂₄-NHS ester

MAL-dPEG®₂₄-NHS ester

Catalog Number:
CR05358075QUA
Mfr. No.:
AQ-10314
Price:
$405
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      • Overview
        • MAL-dPEG®24-NHS ester, product number 10314, is a crosslinking reagent that joins a sulfhydryl to a free amine. The sulfhydryl groups react with a maleimide group via a Michael addition reaction. The amines form amide bonds with the crosslinker by nucleophilic substitution of the N-hydroxysuccinimidyl (NHS) ester of a carboxylic acid group. The maleimide and NHS functional groups on the crosslinking compound sit at either end of a long, discrete-length polyethylene glycol chain (dPEG®).

          The joining of free amines to sulfhydryl groups is one of the most popular, most useful crosslinking reactions in bioconjugate chemistry. These reactions require heterobifunctional reagents that bridge the two groups. Traditional crosslinkers are hydrophobic molecules. Our dPEG® crosslinking products are water-soluble, amphiphilic, single molecular weight PEG compounds with discrete chain lengths.

          The conjugation of conventional hydrophobic crosslinking reagents to biomolecules almost inevitably triggers problems such as aggregation and precipitation of the conjugates. These problems do not occur with our water-soluble, non-immunogenic dPEG® crosslinkers.

          Please contact us at for specific academic pricing.

      • Properties
        • Categories
          Crosslinking Reagents
          CAS Number
          756525-92-5
          Molecular Weight
          1394.55; single compound
          Purity
          > 97%
          Other Properties
          dPEG® Spacer is 82 atoms and 95.2 Å

          * For Research Use Only

      • Reference
        • Greg T. Hermanson, Bioconjugate Techniques, 2nd Edition, Elsevier Inc., Burlington, MA 01803, April, 2008 (ISBN-13: 978-0-12-370501-3; ISBN-10: 0-12-370501-0); See pp. 276-335 for general description and use of heterobifunctional crosslinkers, as well as his specific discussion with protocols of our MAL-dPEG®x-NHS esters on pp. 718-722.

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