2'-Deoxy-2'-fluoro-4-thiouridine

≥95%

Reagent Code: #179611
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CAS Number 10212-16-5

science Other reagents with same CAS 10212-16-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 262.26 g/mol
Formula C₉H₁₁FN₂O₄S
badge Registry Numbers
MDL Number MFCD30570247
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in molecular biology for RNA labeling and tracking due to its photoactivatable properties. When exposed to UV light, it forms covalent bonds with nearby RNA or interacting proteins, enabling the study of RNA-protein interactions and RNA dynamics in live cells. Commonly applied in photo-crosslinking experiments to capture transient RNA interactions. Also utilized in metabolic labeling of newly synthesized RNA to monitor gene expression changes with high temporal resolution. Its fluorine and sulfur modifications enhance stability and detection sensitivity.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿2,890.00

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2'-Deoxy-2'-fluoro-4-thiouridine
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Used in molecular biology for RNA labeling and tracking due to its photoactivatable properties. When exposed to UV light, it forms covalent bonds with nearby RNA or interacting proteins, enabling the study of RNA-protein interactions and RNA dynamics in live cells. Commonly applied in photo-crosslinking experiments to capture transient RNA interactions. Also utilized in metabolic labeling of newly synthesized RNA to monitor gene expression changes with high temporal resolution. Its fluorine and sulfur mo

Used in molecular biology for RNA labeling and tracking due to its photoactivatable properties. When exposed to UV light, it forms covalent bonds with nearby RNA or interacting proteins, enabling the study of RNA-protein interactions and RNA dynamics in live cells. Commonly applied in photo-crosslinking experiments to capture transient RNA interactions. Also utilized in metabolic labeling of newly synthesized RNA to monitor gene expression changes with high temporal resolution. Its fluorine and sulfur modifications enhance stability and detection sensitivity.

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