Improved efficiency for primer extension by using a long, highly-labeled primer generated from immobilized single-stranded DNA templates

Nucleic Acids Research

Volumn 25, Issue 8, 1997, Pages 1658-1659

  Flouriot, Gilles ^a   Pope, Caroline ^b   Kenealy, Mary Rose ^b   Gannon, Frank ^a  

^a EUROPEAN MOLECULAR BIOLOGY LABORATORY   (Germany)

^b NATIONAL UNIVERSITY OF IRELAND   (Ireland)

Author keywords

[No Author keywords available]

Indexed keywords

MESSENGER RNA; PRIMER DNA; SINGLE STRANDED DNA;

ARTICLE; HUMAN; HUMAN CELL; PRIORITY JOURNAL; REVERSE TRANSCRIPTION; RNA ANALYSIS;

ANIMALS; CELL LINE; CHICKENS; DNA PRIMERS; DNA, SINGLE-STRANDED; FEMALE; GENETIC TECHNIQUES; HUMANS; OVIDUCTS; RECEPTORS, ESTROGEN; RNA; TEMPLATES, GENETIC; TUMOR CELLS, CULTURED;

EID: 0030824915     PISSN: 03051048     EISSN: None     Source Type: Journal    
DOI: 10.1093/nar/25.8.1658     Document Type: Article

References (3)

1. Ausubel, F.M., Brent, R., Kingston, R.E., Moore, D.D., Seidman, J.G., Smith, J.A. and Struhl, K. (1987) Current Protocols in Molecular Biology. Greene Publishing Associates and Wiley-Interscience.
2. Green, S., Walter, P., Kumar, V., Krust, A., Bornert, J.M., Argos, P. and Chambon, P. (1986) Nature 320, 134-139.
3. Nestor, P.V., Ford, R.C., Webb, P. and Gannon, F. (1994) J. Sreroid Biochem. Mol. Biol. 50, 121-130.