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Clinical Chemistry, Vol 39, 1408-1411, Copyright © 1993 by American Association for Clinical Chemistry
R Zolfaghari, X Chen and EA Fisher
Department of Biochemistry, Medical College of Pennsylvania, Philadelphia 19129.
We have developed a simple protocol for isolating RNA from both cell culture and tissue from human and animal sources, using guanidine thiocyanate and guanidine hydrochloride, but no organic solvents. The protocol reproducibly yielded 15 to 25 micrograms of high-quality RNA per 10(6) cells of human and animal origin and 1 to 1.1 mg of RNA per gram of human placental tissue. The RNA so obtained was ribonuclease- free and not contaminated by DNA. It was suitable for reverse transcription-polymerase chain reaction, Northern blot analysis, and in vitro expression of proteins. Thus, the molecular assessment of both research and clinical samples can be readily and reliably initiated by the application of this protocol.
The following articles in journals at HighWire Press have cited this article:
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R. Zolfaghari and A. C. Ross Lecithin:retinol acyltransferase from mouse and rat liver: cDNA cloning and liver-specific regulation by dietary vitamin A and retinoic acid J. Lipid Res., December 1, 2000; 41(12): 2024 - 2034. [Abstract] [Full Text] |
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H. D. Dawson, Y. Yamamoto, R. Zolfaghari, F. J. Rosales, J. Dietz, T. Shimada, N.-q. Li, and A. C. Ross Regulation of Hepatic Vitamin A Storage in a Rat Model of Controlled Vitamin A Status during Aging J. Nutr., May 1, 2000; 130(5): 1280 - 1286. [Abstract] [Full Text] |
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W Liedtke, L Battistini, C F Brosnan, and C S Raine A comparison of methods for RNA extraction from lymphocytes for RT-PCR. Genome Res., December 1, 1994; 4(3): 185 - 187. [PDF] |
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