2'-Deoxy-5'-O-DMT-5-(3-methacryloyl)uridine 3'-CE phosphoramidite

≥95%

Reagent Code: #169107
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CAS Number 198080-38-5

science Other reagents with same CAS 198080-38-5

blur_circular Chemical Specifications

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Weight 814.88 g/mol
Formula C₄₃H₅₁N₄O₁₀P
badge Registry Numbers
MDL Number MFCD15145404
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in solid-phase oligonucleotide synthesis, this phosphoramidite derivative enables the site-specific incorporation of a photoreactive uridine analog into DNA strands. The 5-(3-methacryloyl) group acts as a crosslinking agent upon UV irradiation, allowing for the study of nucleic acid-protein interactions or for immobilizing oligonucleotides onto surfaces. The DMT (dimethoxytrityl) group provides temporary 5'-end protection during synthesis, ensuring stepwise chain elongation, while the phosphoramidite moiety facilitates efficient coupling to the growing oligonucleotide chain. Commonly applied in the preparation of functionalized DNA probes, microarrays, and photo-crosslinking studies in molecular biology.

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inventory 25mg
10-20 days ฿7,130.00

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2'-Deoxy-5'-O-DMT-5-(3-methacryloyl)uridine 3'-CE phosphoramidite
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Used in solid-phase oligonucleotide synthesis, this phosphoramidite derivative enables the site-specific incorporation of a photoreactive uridine analog into DNA strands. The 5-(3-methacryloyl) group acts as a crosslinking agent upon UV irradiation, allowing for the study of nucleic acid-protein interactions or for immobilizing oligonucleotides onto surfaces. The DMT (dimethoxytrityl) group provides temporary 5'-end protection during synthesis, ensuring stepwise chain elongation, while the phosphoramidit

Used in solid-phase oligonucleotide synthesis, this phosphoramidite derivative enables the site-specific incorporation of a photoreactive uridine analog into DNA strands. The 5-(3-methacryloyl) group acts as a crosslinking agent upon UV irradiation, allowing for the study of nucleic acid-protein interactions or for immobilizing oligonucleotides onto surfaces. The DMT (dimethoxytrityl) group provides temporary 5'-end protection during synthesis, ensuring stepwise chain elongation, while the phosphoramidite moiety facilitates efficient coupling to the growing oligonucleotide chain. Commonly applied in the preparation of functionalized DNA probes, microarrays, and photo-crosslinking studies in molecular biology.

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