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Biocaxis > Products > Phosphoramidities

 

 

 

DMT-2′O-Methyl-rG(ib) Phosphoramidite configured for MerMade DMT-2′-O-Methyl-rG(ib) Phosphoramidite

Catalog NO.: RNA-OMEPM-003 | CAS NO.: 150780-67-9 | Brand: BIOCAXIS

Category

Carbohydrates, Nucleosides & Nucleotides, RNA Phosphoramidites

Synonyms:

DMT-2′-O-Me-rG(ib) amidite, N-(2-methyl-1-oxopropyl)-5′-O-[bis(4-methoxyphenyl)phenylmethyl]-2′-O-methyl-guanosine, 3′-[2-cyanoethyl N,N-bis(1-methylethyl)phosphoramidite]

Molecular Formula
C45H56N7O9P

Molecular Weight

869.94

General description

Proligo′s 2′O-Methyl RNA monomers are compatible with fast deprotection schemes that are based on the application of aliphatic amines, such as methylamine. The adenosine and guanosine monomers are protected with the standard benzoyl (bz) and isobutyryl (ib) groups.2′O-Methyl RNA is a nucleic acid analogue that is characterized by the exceptional hybridization properties that it imparts with complimentary DNA or RNA, as well as increased stability against enzymatic degradation compared to natural nucleic acids. The unique combination of properties of 2′O-Methyl RNA had found widespread use in the fields of:

Diagnostic probes

Aptamer and ribozyme development

Mixed 2′O-Methyl-RNA/DNA antisense molecule

Key Features:

High yield of crude oligonucleotides

Compatible with DNA synthesis

Can be employed together with DNA or RNA phosphoramidites in the same synthesis to produce mixmer oligonucleotides

Recommended deprotection conditions are 8 hours at 55 °C using concentrated ammonia solution, or with AMA (concentrated ammonia/40% aqueous methylamine I/I, v/v) for 10 minutes at 65 °C

Purification and other downstream processing of fully modified 2′OMethyl RNA oligonucleotides are simpler than in the case of RNA, as no special precautions are required to provide protection against nucleolyticdegradationDMT-2′O-Methyl-rG(ib) Phosphoramidite

 

Usage

Solid phase synthesis of DNA and RNA oligonucleotides in chemical or enzymatic processes.

 

 

 

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