Methods for the preparation of large quantities of complex single-stranded oligonucleotide libraries

PLoS ONE

Volumn 9, Issue 4, 2014, Pages

  Murgha, Yusuf E ^a   Rouillard, Jean Marie ^a   Gulari, Erdogan ^a  

^a UNIVERSITY OF MICHIGAN   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

OLIGONUCLEOTIDE; COMPLEMENTARY DNA; RNA; SINGLE STRANDED DNA; STREPTAVIDIN;

ALKALINE DENATURATION METHOD; ANALYTIC METHOD; ARTICLE; BINDING SITE; BIOTINYLATION; CONTROLLED STUDY; DENATURATION; ENZYME INACTIVATION; ENZYME PURIFICATION; GENE AMPLIFICATION; GENETIC TRANSCRIPTION; HYDROLYSIS; IN VITRO TRANSCRIPTION AND REVERSE TRANSCRIPTION METHOD; INTERMETHOD COMPARISON; LAMBDA EXONUCLEASE METHOD; METHODOLOGY; MICROARRAY ANALYSIS; MOLECULAR RECOGNITION; POLYMERASE CHAIN REACTION; PROTEIN BINDING; PROTEIN DATABASE; PROTEIN PHOSPHORYLATION; CHEMISTRY; COMPARATIVE STUDY; DNA MICROARRAY; GENE LIBRARY; GENETIC PROCEDURES; GENETICS; METABOLISM; MOLECULAR GENETICS; NUCLEOTIDE SEQUENCE; PROTEIN ENGINEERING; RNA INTERFERENCE;

BASE SEQUENCE; BIOTINYLATION; DNA, COMPLEMENTARY; DNA, SINGLE-STRANDED; GENE LIBRARY; GENETIC TECHNIQUES; HYDROLYSIS; MOLECULAR SEQUENCE DATA; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; OLIGONUCLEOTIDES; POLYMERASE CHAIN REACTION; PROTEIN ENGINEERING; RNA; RNA INTERFERENCE; STREPTAVIDIN;

EID: 84899623691     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0094752     Document Type: Article

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