Biotin-dPEG®₃-oxyamine. HCl

Biotin-dPEG®₃-oxyamine. HCl

Catalog Number:
BR01357808QUA
Mfr. No.:
AQ-11100
Price:
$240
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      • Overview
        • Biotin-dPEG®3-oxyamine·HCl, product number 11100, forms a stable oxime bond when conjugated to a ketone or aldehyde. Using this product permits biotinylation of the carbohydrate coats of glycoproteins.

          Biotinylation
          Biotinylation is the process of covalently attaching biotin to a molecule such as a peptide, protein, or nucleic acid, or surfaces such as glass or gold. Bioconjugation research and product development and numerous clinical assays use biotinylated molecules. The amphiphilic dPEG® linker of Biotin-dPEG®3-oxyamine·HCl imparts excellent water solubility to biotin, which is usually poorly soluble in water.

          An aminooxy group (also known as an alkoxyamine) consists of a primary terminal amine adjacent to oxygen (i.e., —ONH2). This group reacts selectively and efficiently with aldehydes to form an aldoxime linkage and with ketones to form a ketoxime linkage. An oxime bond is more stable than a hydrazone bond and does not need to be reduced to a secondary amine to stabilize it.

          Aldehydes and ketones occur relatively rarely in nature; however, using sodium periodate, aldehydes can be formed in glycoproteins whose carbohydrate coats contain reducing sugars. Moreover, scientific literature examples demonstrate the introduction of ketones into bacterial cell walls through liposomal fusion.

          Some commercially available biotin-aminooxy products use either no spacer or a hydrophobic, alkyl chain as a spacer between biotin and the aminooxy moiety. Such products have poor solubility in water and must be dissolved in a dry organic solvent such as dimethyl sulfoxide (DMSO) immediately before use, which can be problematic under some conditions. If used on proteins, these hydrophobic products may trigger aggregation and precipitation of the biotinylated molecule. Even if aggregation and precipitation do not occur, the hydrophobic spacer can contribute to non-specific binding. Because it is amphiphilic, Biotin-dPEG®3-oxyamine·HCl can be dissolved in water or aqueous buffer and used directly in a conjugation reaction. PN11100 will not cause aggregation or precipitation of the biotinylated molecule. Moreover, the hydrophilicity of the dPEG® linker reduces or eliminates non-specific binding.

          We sell Biotin-dPEG®3-oxyamine·HCl as the hydrochloride salt. A longer version of this product, PN11102, Biotin-dPEG®11-oxyamine·HCl, is also available.

          If you need bulk product in a larger package size than our standard sizes, please contact us for a quote. Our commercial capabilities permit us to manufacture this product at any scale that you need.

          Please contact us at for specific academic pricing.

      • Properties
        • Categories
          Biotinylation Reagents
          Molecular Weight
          471.01; single compound
          Purity
          > 98%
          Other Properties
          dPEG® Spacer is 14 atoms and 16.6 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, and the specific sample protocol for SPDP and LC-SPDP on pp. 286-288. See Greg’s extensive index on pp. 1192-1193 for references to a number and range of applications and their respective protocols.

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