5'-O-(Dimethoxytrityl)-5-[N-(6-(trifluoroacetamido)hexyl)-3-(E)-acrylamido]-2'-deoxyuridine
97%
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This compound is primarily used in the synthesis of modified oligonucleotides, particularly in the field of molecular biology and genetic research. It serves as a key building block in the preparation of DNA probes and primers, enabling the study of gene expression, mutation analysis, and nucleic acid interactions. The dimethoxytrityl (DMT) group provides protection during solid-phase oligonucleotide synthesis, ensuring selective reactivity at specific sites. The trifluoroacetamidohexyl and acrylamido moieties facilitate further functionalization, such as conjugation with fluorescent dyes or other biomolecules, enhancing applications in diagnostics, biosensors, and targeted drug delivery systems. Its unique structure also makes it valuable in developing therapeutic oligonucleotides for gene silencing or editing technologies.
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