Modification of the Standard Trizol-Based Technique Improves the Integrity of RNA Isolated from RNase-Rich Placental Tissue
Author:
Affiliation:
1. Department of Cell, and Tissue Biology Department of Obstetrics, Gynecology, and Reproductive Sciences, Department of Anatomy, and, Department of, Pharmaceutical Chemistry, University of California, San Francisco, CA
Publisher
Oxford University Press (OUP)
Subject
Biochemistry (medical),Clinical Biochemistry
Link
http://academic.oup.com/clinchem/article-pdf/52/1/159/32685417/clinchem0159.pdf
Reference6 articles.
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2. Auer H, Lyianarachchi S, Newsom D, Klisovic MI, Marcucci G, Kornacker K, et al. Chipping away at the chip bias: RNA degradation in microarray analysis. Nat Genet2003;35:292-293.
3. Chirgwin JM, Praybyla AE, MacDonald RJ, Rutter WJ. Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease. Biochemistry1979;18:5294-5299.
4. Krosting J, Latham G. RNase activity in mouse tissue: classification, hierarchy, and methods for control. Ambion TechNotes, Vol. 12, issue 32005 Ambion Austin, TX. .
5. Van de Goor TA. The principle and promise of labchip technology. Pharma Genomics2003;3:16-18.
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