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  • High-throughput chemical modification of oligonucleotides for systematic structure-activity relationship evaluation.

High-throughput chemical modification of oligonucleotides for systematic structure-activity relationship evaluation.

Bioconjugate chemistry (2014-11-15)
Daniel Zewge, Francis Gosselin, Denise M Kenski, Jenny Li, Vasant Jadhav, Yu Yuan, Sandhya S Nerurkar, David M Tellers, W Michael Flanagan, Ian W Davies
ABSTRACT

Chemical modification of siRNA is achieved in a high-throughput manner (96-well plate format) by copper catalyzed azide-alkyne cycloadditions. This transformation can be performed in one synthetic operation at up to four positions with complete specificity, good yield, and acceptable purity. As demonstrated here, this approach extends the current synthetic options for oligonucleotide modifications and simultaneously facilitates the systematic, rapid biological evaluation of modified siRNA.

MATERIALS
Product Number
Brand
Product Description

Supelco
Citric acid, Anhydrous, Pharmaceutical Secondary Standard; Certified Reference Material
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Acetic anhydride, Arxada quality, ≥99.5% (GC)
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Iodine, 99.999% trace metals basis
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Citric acid, ≥99.5%, FCC, FG
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Acetic anhydride, LiChropur, ≥99.0%
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Dichloromethane, analytical standard
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Pyridine, analytical standard
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Pyridine, ≥99%
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Imidazole buffer Solution, BioUltra, 1 M in H2O
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Iodine, ≥99.99% trace metals basis
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N,N-Dimethylacetamide, ReagentPlus®, ≥99%
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Citric acid, anhydrous, suitable for cell culture, suitable for plant cell culture
Citric acid, anhydrous, European Pharmacopoeia (EP) Reference Standard
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Acetonitrile, electronic grade, 99.999% trace metals basis
USP
Citric acid, United States Pharmacopeia (USP) Reference Standard
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Acetonitrile, suitable for DNA synthesis, ≥99.9% (GC)
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Iodine, ReagentPlus®, ≥99.8% (titration)
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