5'-O-DMTr-2'-O-TMBTM-U-3'-O-succinate, TEA salt

Basic Information
Place of Origin: China
Price: Negotiable
Packaging Details: 10g, 100g, 1000g, 5kg , 25kg
Delivery Time: 7-15 workdays
Payment Terms: LC, T/T, PayPal, Western Union, Small-amount payment, Money Gram
Supply Ability: 500kg/Month
Highlight:

5'-O-DMTr-2'-O-TMBTM-U-3'-O-succinate

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2'-O-TMBTM Succinates TEA salt

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HPLC 98.0% TEA salt

 

White to off-white powder,2-8℃,HPLC≥98.0%

 

 

Product Name: 5'-O-DMTr-2'-O-TMBTM-U-3'-O-succinate, TEA salt

 

Product Description:

 

5'-O-DMTr-2'-O-TMBTM-U-3'-O-succinate, TEA salt is a high-quality nucleotide phosphoramidite used in oligonucleotide synthesis and molecular biology research. It incorporates a modified uridine nucleotide analog with a succinate linker, a 5'-O-dimethoxytrityl (DMTr) protecting group, and a 2'-O-tert-butyldimethylsilyl (TMBTM) modification. The TEA (Triethylammonium) salt form enhances solubility and facilitates efficient synthesis. This phosphoramidite offers improved stability and controlled incorporation during oligonucleotide synthesis. 5'-O-DMTr-2'-O-TMBTM-U-3'-O-succinate, TEA salt is compatible with standard synthesis protocols and can be used with automated DNA synthesizers. It provides researchers with a valuable tool for the synthesis of modified DNA oligonucleotides for various applications in molecular biology research.

 

 

Parameter Table:

 

Parameter Description
Composition Nucleotide phosphoramidite with modified uridine nucleotide analog, succinate linker, 5'-O-dimethoxytrityl (DMTr) protecting group, and 2'-O-tert-butyldimethylsilyl (TMBTM) modification
Purity High purity
Solubility Soluble in typical organic solvents
Stability Enhanced stability during synthesis and storage
Compatibility Compatible with standard oligonucleotide synthesis protocols and automated DNA synthesizers
Applications 1. Site-specific incorporation of modified uridine analogs
  2. Development of modified DNA oligonucleotides for functional studies
  3. Probing RNA structure and interactions
  4. Nucleotide modifications for improved RNA stability and resistance

Contact Details
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