Applying a highly specific and reproducible cDNA RDA method to clone garlic up-regulated genes in human gastric cancer cells

doi:10.3748/wjg.v8.i2.213

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Apr 15, 2002 (publication date) through Dec 17, 2024

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World Journal of Gastroenterology

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1007-9327

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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA

Gastric Cancer

World J Gastroenterol. Apr 15, 2002; 8(2): 213-216
Published online Apr 15, 2002. doi: 10.3748/wjg.v8.i2.213

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Figure 3 Agarose gel electrophoresis of amplicons derived from different enzyme digestions. A: The amplicons obtained by using BamH I to digest Alli823 (lane 1) and BGC823 (lane 2) cDNA library DNAs respectively; B: The amplicons obtained by using BamH I and Xho I together to digest Alli823 (lane 1) and BGC823 (lane 2) library DNAs respectively. 1 kb size marker (lane M).

Citation: Li Y, Lu YY. Applying a highly specific and reproducible cDNA RDA method to clone garlic up-regulated genes in human gastric cancer cells. World J Gastroenterol 2002; 8(2): 213-216
URL: https://www.wjgnet.com/1007-9327/full/v8/i2/213.htm
DOI: https://dx.doi.org/10.3748/wjg.v8.i2.213