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High-performance liquid chromatography of oligoguanylates at high pHBecause of the stable self-structures formed by oligomers of guanosine, standard high-performance liquid chromatography techniques for oligonucleotide fractionation are not applicable. Previously, oligoguanylate separations have been carried out at pH 12 using RPC-5 as the packing material. While RPC-5 provides excellent separations, there are several limitations, including the lack of a commercially available source. This report describes a new anion-exchange high-performance liquid chromatography method using HEMA-IEC BIO Q, which successfully separates different forms of the guanosine monomer as well as longer oligoguanylates. The reproducibility and stability at high pH suggests a versatile role for this material.
Document ID
20040090103
Acquisition Source
Legacy CDMS
Document Type
Reprint (Version printed in journal)
Authors
Stribling, R.
(University of California at Davis 95616 United States)
Deamer, D.
Date Acquired
August 21, 2013
Publication Date
January 1, 1991
Publication Information
Publication: Journal of chromatography
Volume: 538
ISSN: 0021-9673
Subject Category
Exobiology
Funding Number(s)
CONTRACT_GRANT: N0001490-1121
Distribution Limits
Public
Copyright
Other
Keywords
Non-NASA Center
NASA Discipline Number 52-20
NASA Program Exobiology
NASA Discipline Exobiology

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