๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Analysis of nucleic acid bases by high-performance liquid ion chromatography

โœ Scribed by V.P. Demushkin; Yu.G. Plyashkevich


Publisher
Elsevier Science
Year
1978
Tongue
English
Weight
297 KB
Volume
84
Category
Article
ISSN
0003-2697

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


High-Throughput Analysis of Nucleic Acid
โœ Mark J. Dickman; Maryam M. Matin; David P. Hornby ๐Ÿ“‚ Article ๐Ÿ“… 2002 ๐Ÿ› Elsevier Science ๐ŸŒ English โš– 101 KB

Ion-pair reverse-phase high-performance liquid chromatography is presented as a versatile platform for the rapid analysis of nucleic acid modification reactions in a high-throughput manner. This system allows both sensitive and nonradioactive assays to be developed for a variety of nucleic acid modi

High performance separations of nucleic
โœ Baba, Yoshinobu ;Tsuhako, Mitsutomo ;Enomoto, Shigeru ;Chin, A. Michael ;Dubrow, ๐Ÿ“‚ Article ๐Ÿ“… 1991 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 418 KB ๐Ÿ‘ 2 views

## Abstract High resolution separations of nucleic acids have been performed using high performance capillary electrophoresis (HPCE) and high performance liquid chromatography (HPLC). Electropherograms showing HPCE separations of single and double stranded DNA are presented and compared with HPLC s

Proteoglycan analysis by high-performanc
โœ Edith R. Schwartz; Jeff Stevens; Donald E. Schmidt Jr. ๐Ÿ“‚ Article ๐Ÿ“… 1981 ๐Ÿ› Elsevier Science ๐ŸŒ English โš– 412 KB

Three different well-characterized preparations of proteoglycan subunits were analyzed by high-performance liquid chromatography on a silica-based material bonded with an amide phase. The biochemical integrity of the proteoglycan subunits was retained during this procedure. The high sensitivity coup

Analysis of triacylglycerol positional i
โœ Adlof, Richard O. ๐Ÿ“‚ Article ๐Ÿ“… 1995 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 345 KB

## Abstract Silver ion chromatography, utilizing two commercially available HPLC columns connected in series, was used to separate a variety of triacylglycerol positional isomers. The isomers had a fatty acid composition of ABA and AAB, where A and B were fatty acids containing zero to three double