A protocol for differential display of mRNA expression using either fluorescent or radioactive labeling

Nature Protocols

Volumn 2, Issue 3, 2007, Pages 457-470

  Liang, Peng ^a,b   Meade, Jonathan D ^a   Pardee, Arthur B ^c  

^a GenHunter Corporation   (United States)

^b VANDERBILT UNIVERSITY   (United States)

^c HARVARD MEDICAL SCHOOL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; FLUORESCENT DYE; MESSENGER RNA; POLYADENYLATED RNA; RADIOISOTOPE;

ACCURACY; ARTICLE; DENATURING GRADIENT GEL ELECTROPHORESIS; DIFFERENTIAL DISPLAY; DNA MICROARRAY; DNA SEQUENCE; EUKARYOTE; GEL ELECTROPHORESIS; GENE EXPRESSION; GENE EXPRESSION PROFILING; HIGH THROUGHPUT SCREENING; ISOTOPE LABELING; MOLECULAR BIOLOGY; MOLECULAR CLONING; NUCLEIC ACID ANALYSIS; POLYADENYLATION; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PROCESS OPTIMIZATION; QUANTITATIVE ANALYSIS; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; RNA ISOLATION; RNA PURIFICATION; SENSITIVITY AND SPECIFICITY; TIME; AGAR GEL ELECTROPHORESIS; FLUORESCENCE; METABOLISM; METHODOLOGY; POLYACRYLAMIDE GEL ELECTROPHORESIS;

EUKARYOTA;

CLONING, MOLECULAR; ELECTROPHORESIS, AGAR GEL; ELECTROPHORESIS, POLYACRYLAMIDE GEL; FLUORESCENCE; GENE EXPRESSION PROFILING; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; RNA, MESSENGER;

EID: 34347232734     PISSN: 17542189     EISSN: 17502799     Source Type: Journal    
DOI: 10.1038/nprot.2007.46     Document Type: Article

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