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huh7 human hepatoma cells  (ATCC)


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    ATCC huh7 human hepatoma cells
    Huh7 Human Hepatoma Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 31385 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/huh7 human hepatoma cells/product/ATCC
    Average 99 stars, based on 31385 article reviews
    huh7 human hepatoma cells - by Bioz Stars, 2026-03
    99/100 stars

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    OTUD4 and TRIM21 alter the production of subviral particles and virions. (A, B, E, F) Lysates were prepared from Huh7 and <t>HepG2</t> cells co-transfected with plasmids encoding 1.2HBV and either TRIM21-myc ( A, B ) or OTUD4-myc ( E, F ). These lysates were subjected to immunoblotting using antibodies against myc, β-actin, and SHBs, and intracellular HBV DNA levels were quantified by qPCR. Additionally, cell culture supernatants were analyzed by qPCR to quantify extracellular HBV DNA and virion DNA levels. (C, D, G, H) Lysates from cells transfected with plasmids encoding 1.2HBV and siRNA targeting either TRIM21 ( C, D ) or OTUD4 ( G, H ) were similarly processed. The lysates were immunoblotted using the indicated antibodies, and intracellular HBV DNA was quantified by qPCR. qPCR was performed on the supernatants to measure HBV DNA and virion DNA levels.
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    OTUD4 and TRIM21 alter the production of subviral particles and virions. (A, B, E, F) Lysates were prepared from Huh7 and HepG2 cells co-transfected with plasmids encoding 1.2HBV and either TRIM21-myc ( A, B ) or OTUD4-myc ( E, F ). These lysates were subjected to immunoblotting using antibodies against myc, β-actin, and SHBs, and intracellular HBV DNA levels were quantified by qPCR. Additionally, cell culture supernatants were analyzed by qPCR to quantify extracellular HBV DNA and virion DNA levels. (C, D, G, H) Lysates from cells transfected with plasmids encoding 1.2HBV and siRNA targeting either TRIM21 ( C, D ) or OTUD4 ( G, H ) were similarly processed. The lysates were immunoblotted using the indicated antibodies, and intracellular HBV DNA was quantified by qPCR. qPCR was performed on the supernatants to measure HBV DNA and virion DNA levels.

    Journal: Journal of Virology

    Article Title: Ubiquitin-dependent proteasomal degradation of small hepatitis B virus surface antigen mediated by TRIM21 and antagonized by OTUD4

    doi: 10.1128/jvi.02309-24

    Figure Lengend Snippet: OTUD4 and TRIM21 alter the production of subviral particles and virions. (A, B, E, F) Lysates were prepared from Huh7 and HepG2 cells co-transfected with plasmids encoding 1.2HBV and either TRIM21-myc ( A, B ) or OTUD4-myc ( E, F ). These lysates were subjected to immunoblotting using antibodies against myc, β-actin, and SHBs, and intracellular HBV DNA levels were quantified by qPCR. Additionally, cell culture supernatants were analyzed by qPCR to quantify extracellular HBV DNA and virion DNA levels. (C, D, G, H) Lysates from cells transfected with plasmids encoding 1.2HBV and siRNA targeting either TRIM21 ( C, D ) or OTUD4 ( G, H ) were similarly processed. The lysates were immunoblotted using the indicated antibodies, and intracellular HBV DNA was quantified by qPCR. qPCR was performed on the supernatants to measure HBV DNA and virion DNA levels.

    Article Snippet: The human hepatoma cell lines HepG2 and Huh7 were sourced from the American Type Culture Collection (Manassas, VA, USA) and the Japanese Collection of Research Bioresources Cell Bank (Osaka, Japan), respectively, while HUVECs were generously provided by Dr. Huang ( ).

    Techniques: Transfection, Western Blot, Cell Culture