Establishment of a cell-based assay system for hepatitis C virus serine protease and its primary applications

doi:10.3748/wjg.v9.i11.2474

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Nov 15, 2003 (publication date) through Nov 4, 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

Viral Hepatitis

World J Gastroenterol. Nov 15, 2003; 9(11): 2474-2479
Published online Nov 15, 2003. doi: 10.3748/wjg.v9.i11.2474

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Figure 6 Northern blot analysis of NS3/4A mRNA level in transfected Cos7 cells (Lane 1, 3, 5) and HepG2 cells (Lane 2, 4, 6). Lane 1, 2 pCI-neo-NS3/4A-SEAP (1b type); Lane 3, 4 pCI-neo-NS3/4A (TGA) (control); Lane 5, 6 pCI-neo-RNS3/4A-SEAP (1a type); Intensity of hybridization signal was measured by densitometry, and the relative intensities of NS3/4A signal to β-actin are indicated below the lane No.

Citation: Mao HX, Lan SY, Hu YW, Xiang L, Yuan ZH. Establishment of a cell-based assay system for hepatitis C virus serine protease and its primary applications. World J Gastroenterol 2003; 9(11): 2474-2479
URL: https://www.wjgnet.com/1007-9327/full/v9/i11/2474.htm
DOI: https://dx.doi.org/10.3748/wjg.v9.i11.2474