Chum-RNA allows preparation of a high-quality cDNA library from a single-cell quantity of mRNA without PCR amplification

Nucleic Acids Research

Volumn 36, Issue 15, 2008, Pages

  Tougan, Takahiro ^a   Okuzaki, Daisuke ^a   Nojima, Hiroshi ^a  

^a OSAKA UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

CHUM RNA; COMPLEMENTARY DNA; MESSENGER RNA; RNA; BACTERIOPHAGE T7 RNA POLYMERASE; DNA DIRECTED RNA POLYMERASE; VIRUS PROTEIN;

ANALYTIC METHOD; ARTICLE; CONTROLLED STUDY; DNA DETERMINATION; DNA LIBRARY; DNA SYNTHESIS; GENE ACTIVATION; MICHAELIS CONSTANT; MOLECULAR CLONING; NUCLEIC ACID AMPLIFICATION; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; QUANTITATIVE ANALYSIS; BIOSYNTHESIS; DNA MICROARRAY; GENE EXPRESSION PROFILING; GENE LIBRARY; HUMAN; METHODOLOGY;

MAMMALIA;

DNA, COMPLEMENTARY; DNA-DIRECTED RNA POLYMERASES; GENE EXPRESSION PROFILING; GENE LIBRARY; HUMANS; NUCLEIC ACID AMPLIFICATION TECHNIQUES; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; POLYMERASE CHAIN REACTION; RNA, MESSENGER; VIRAL PROTEINS;

EID: 50849084092     PISSN: 03051048     EISSN: 13624962     Source Type: Journal    
DOI: 10.1093/nar/gkn420     Document Type: Article

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