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 Nov 12, 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 4 A: Agarose gel electrophoresis of reamplified difference products SH1-4 (lanes 1-4 respectively). PCR product of GAPDH (400 bp in size) used as quantity control (lane G); B: Slot blots analysis showing differentially expressed cDNAs. Reverse transcription products (first stranded cDNA) of total RNA of BGC823 and Alli823 cells used as probe respectively; C: The degree to which each cDNA was up-regulated.

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