RNA analysis by ion-pair reversed-phase high performance liquid chromatography

Nucleic Acids Research

Volumn 29, Issue 2, 2021, Pages

  Azarani, Arezou ^a   Hecker, Karl H ^a  

^a TRANSGENOMIC INC   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DIGOXIGENIN; MESSENGER RNA; POLYADENYLATED RNA; RIBOSOME RNA; RNA; CAPSID PROTEIN; COLORING AGENT; RNA BINDING PROTEIN; VIRUS RNA;

ARTICLE; CONTROLLED STUDY; INTERMETHOD COMPARISON; ION PAIR CHROMATOGRAPHY; MOLECULAR SIZE; MOUSE; NONHUMAN; PRIORITY JOURNAL; QUANTITATIVE ANALYSIS; RELIABILITY; REVERSED PHASE HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; RNA ANALYSIS; RNA DEGRADATION; RNA LADDER; RNA PURIFICATION; RNA STABILITY; RNA STRUCTURE; RNA TRANSCRIPTION; ANIMAL; BRAIN LEVEL; CHEMISTRY; COLIPHAGE; DNA DENATURATION; GENETIC TRANSCRIPTION; GENETICS; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; INSTRUMENTATION; ISOLATION AND PURIFICATION; METHODOLOGY; VIRUS CAPSID;

ANIMALS; BRAIN CHEMISTRY; CAPSID; CAPSID PROTEINS; CHROMATOGRAPHY, HIGH PRESSURE LIQUID; COLORING AGENTS; DIGOXIGENIN; LEVIVIRUS; MICE; NUCLEIC ACID DENATURATION; RNA; RNA, MESSENGER; RNA, VIRAL; RNA-BINDING PROTEINS; TRANSCRIPTION, GENETIC;

MLCS; MLOWN;

EID: 0035864172     PISSN: 03051048     EISSN: 13624962     Source Type: Journal    
DOI: 10.1093/nar/29.2.e7     Document Type: Article

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