Literature DB >> 2101916

New reagents and solid support for automated oligonucleotide synthesis.

H Vu1, C McCollum, C Lotys, A Andrus.   

Abstract

The optimal system for the rapid, efficient, convenient, and economical synthesis and purification of synthetic oligonucleotides has been advancing. By recognizing the very rapid reaction kinetics and taking advantage of an efficient, low volume delivery system, cycle times have decreased to about 5.5 minutes, without compromising synthesis performance. A new set of base protecting groups for cyanoethylphosphoramidite nucleoside monomers have been developed, which decreases the post-synthesis time requirements. A particular form of polystyrene has also been developed as a solid support for automated oligonucleotide synthesis. Typical sequencing or PCR primers (20mers) now require less than 2 hours for synthesis and 2 hours for cleavage and deprotection.

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Year:  1990        PMID: 2101916

Source DB:  PubMed          Journal:  Nucleic Acids Symp Ser        ISSN: 0261-3166


  2 in total

1.  Chemical synthesis of RNA using fast oligonucleotide deprotection chemistry.

Authors:  R Vinayak; P Anderson; C McCollum; A Hampel
Journal:  Nucleic Acids Res       Date:  1992-03-25       Impact factor: 16.971

2.  Development of a Novel Fluorescence Assay Based on the Use of the Thrombin-Binding Aptamer for the Detection of O-Alkylguanine-DNA Alkyltransferase Activity.

Authors:  Maria Tintoré; Anna Aviñó; Federico M Ruiz; Ramón Eritja; Carme Fàbrega
Journal:  J Nucleic Acids       Date:  2010-09-14
  2 in total

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