SCOPUS 정보 검색 플랫폼

Volumn 313, Issue 1, 2003, Pages 128-132

High-performance liquid chromatography purification of 26-bp serial analysis of gene expression ditags results in higher yields, longer concatemers, and substantial time savings

(3) Damgaard Nielsen, Mette a Millichip, Mark b Josefsen, Knud a

a Mental Health Services CPH (Denmark)

b Polymer Laboratories Ltd (United Kingdom)

Author keywords

Ditags; HPLC; Polystyrene divinylbenzene; Purification; SAGE

Indexed keywords

CLONE CELLS; CLONING; ELECTROPHORESIS; GENE EXPRESSION; POLYSTYRENES; PURIFICATION;

DITAGS; HIGH MOLECULAR WEIGHT; HPLC; POLYACRYLAMIDE GEL ELECTROPHORESIS; REVERSE PHASE HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; SAGE; SERIAL ANALYSIS OF GENE EXPRESSIONS; TETRAETHYLAMMONIUM ACETATES;

HIGH PERFORMANCE LIQUID CHROMATOGRAPHY;

ACETIC ACID DERIVATIVE; ACETONITRILE; BUFFER; DIVINYLBENZENE; ENZYME; POLYSTYRENE; TETRYLAMMONIUM ACETATE; UNCLASSIFIED DRUG;

ARTICLE; DEVICE; ENZYMATIC DEGRADATION; EXPOSURE; GEL; GENE EXPRESSION; GENE LIBRARY; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; METHODOLOGY; MOLECULAR CLONING; MOLECULAR WEIGHT; POLYACRYLAMIDE GEL ELECTROPHORESIS; PRIORITY JOURNAL; PURIFICATION; TIME;

SALVIA;

EID: 0037325710 PISSN: 00032697 EISSN: None Source Type: Journal
DOI: 10.1016/S0003-2697(02)00511-0 Document Type: Article

Times cited : (6)

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