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 Jul 15, 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 2 Agarose gel electrophoresis of digestion products of Alli823 (lanes 1, 3, 5) and BGC823 (lanes 2, 4, 6) cDNA library DNAs digested with BamH I at 37 °C for 2 (lanes 1, 2), 4 (lanes 3, 4), and 12 h (lanes 5, 6) respectively. The digestion products of Alli823 (lane 7) and BGC823 (lane 8) library DNAs digested with BamH I and Xho I together (A fragment, 850 bp in size, appeared in the digestion products). λPhage/Hind III 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