Aniline Oligonucleotide Modification
Bio-Synthesis offers aniline modificat at 5' and 3' end of an oligonucloeitde. Aniline modified oligonucleotide can function as an amino or diazo linker. Oligo modified with aniline can acts as a catalyst inthe hydrazide-aldehyde reactions. The aromatic amine of aniline rapidly and efficiently forms a Schiff base with the aldehyde, effectively increasing the activation of the aldehyde. As a result, the aniline is easily replaced by the hydrazide. Thus, aniline (also called GlycoLink Coupling Catalyst) allows significantly greater total coupling yields with hydrazides and/or greater efficiency (i.e., equal yields with less hydrazide reagent).
See the following references for additional information about aniline catalysis:
- Byeon, J.Y., et al. (2010). Efficient bioconjugation of protein capture agents to biosensor surfaces using aniline-catalyzed hydrazone ligation.
- Langmuir 26(19):15430-5. Dirksen, A., et al. (2006). Nucleophilic catalysis of hydrazone formation and transimination: implications for dynamic covalent chemistry. J. Am. Chem. Soc. 128(49):15602-3.
- Dirksen, A., Dawson, PE. (2008). Rapid oxime and hydrazone ligations with aromatic aldehydes for biomolecular labeling. Bioconjug. Chem. 19(12):2543-8.
Product Information
Aniline Oligonucleotide Modification
linker, amino linker, diazo-linker
120.04 (100.0%), 121.05 (7.7%)
C 69.99; H, 5.03; N, 11.66; O, 13.32
-20°C To -70°C
Oligonucleotides are stable in solution at 4°C for up to 2 weeks. Properly reconstituted material stored at -20°C should be stable for at least 6 months. Dried DNA (when kept at -20°C) in a nuclease-free environment should be stable for years.
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