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BioResource International Inc murine hepatocyte cell line fl83b
Murine Hepatocyte Cell Line Fl83b, supplied by BioResource International Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/murine+fl83b+hepatocyte+cell+line/fl83b+cells/pm39863023-210-1-10
Average 90 stars, based on 1 article reviews
murine hepatocyte cell line fl83b - by Bioz Stars, 2026-10
90/100 stars

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Article Title: Acacetin Protects against Non-Alcoholic Fatty Liver Disease by Regulating Lipid Accumulation and Inflammation in Mice.
Article Snippet: The Murine FL83B hepatocyte cell line was purchased from the Bioresource Collection and Research Center (Taiwan).



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BioResource International Inc murine hepatocyte cell line fl83b
Murine Hepatocyte Cell Line Fl83b, supplied by BioResource International Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/murine+fl83b+hepatocyte+cell+line/fl83b+cells/pm39863023-210-1-10
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ATCC li ve r fl83b murine hepatocyte cell line 4 0 e 03
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ATCC murine hepatocyte cell line fl83b
pilF and pilT contribute to host cell adherence. Cells were treated with cytochalasin D to inhibit the internalization of bacteria and then infected with wild-type LVS (WT), DTLB (ΔpilF), DTLB complemented with pilF (ΔpilF/pGPB), or the pilT::HimarFT mutant. The graphs show the CFU of bacteria that adhered to murine bone marrow-derived macrophages (A), A549 human lung epithelial cells (B), and <t>FL83B</t> murine hepatocytes (C). Error bars indicate the standard deviation of triplicate samples. P values were calculated by using a paired t test, comparing DTLB or pilT:HimarFT with the wild-type LVS or comparing DTLB/pGPB with DTLB (*, P < 0.05; **, P < 0.02).
Murine Hepatocyte Cell Line Fl83b, supplied by ATCC, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/murine+fl83b+hepatocyte+cell+line/FL83B/pmc02446743-138-1-22
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ATCC murine hepatocyte cell line
FIG. 7. In vitro adenoviral gene delivery to human and mouse hepatocytes. Human hepatocarcinoma cells, HepG2 (A), the mouse <t>hepatocyte</t> cell line, FL83B (B), or primary CD-1 mouse hepatocytes (C) were infected with each adenoviral vector from 0 up to 12,500 particles per cell (PPC) of Av3nBg (open circle) or Av3nBgFKO1 (filled circle) for 1 hour at 37C. After 24 hours the cells were fixed and stained with X-gal. The percentage of transduced cells was determined per high-power field for each vector dose. The data represent the mean percentage of transduction ± SD (n = 3 wells) from one representative experiment.
Murine Hepatocyte Cell Line, supplied by ATCC, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/murine+fl83b+hepatocyte+cell+line/FL83B/pm12027562-290-15-19
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murine hepatocyte cell line - by Bioz Stars, 2026-10
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pilF and pilT contribute to host cell adherence. Cells were treated with cytochalasin D to inhibit the internalization of bacteria and then infected with wild-type LVS (WT), DTLB (ΔpilF), DTLB complemented with pilF (ΔpilF/pGPB), or the pilT::HimarFT mutant. The graphs show the CFU of bacteria that adhered to murine bone marrow-derived macrophages (A), A549 human lung epithelial cells (B), and FL83B murine hepatocytes (C). Error bars indicate the standard deviation of triplicate samples. P values were calculated by using a paired t test, comparing DTLB or pilT:HimarFT with the wild-type LVS or comparing DTLB/pGPB with DTLB (*, P < 0.05; **, P < 0.02).

Journal:

Article Title: Type IV Pili in Francisella tularensis : Roles of pilF and pilT in Fiber Assembly, Host Cell Adherence, and Virulence ▿

doi: 10.1128/IAI.01726-07

Figure Lengend Snippet: pilF and pilT contribute to host cell adherence. Cells were treated with cytochalasin D to inhibit the internalization of bacteria and then infected with wild-type LVS (WT), DTLB (ΔpilF), DTLB complemented with pilF (ΔpilF/pGPB), or the pilT::HimarFT mutant. The graphs show the CFU of bacteria that adhered to murine bone marrow-derived macrophages (A), A549 human lung epithelial cells (B), and FL83B murine hepatocytes (C). Error bars indicate the standard deviation of triplicate samples. P values were calculated by using a paired t test, comparing DTLB or pilT:HimarFT with the wild-type LVS or comparing DTLB/pGPB with DTLB (*, P < 0.05; **, P < 0.02).

Article Snippet: The murine hepatocyte cell line FL83B, derived from the normal liver of a 15- to 17-day-old fetal mouse, was purchased from the ATCC.

Techniques: Bacteria, Infection, Mutagenesis, Derivative Assay, Standard Deviation

FIG. 7. In vitro adenoviral gene delivery to human and mouse hepatocytes. Human hepatocarcinoma cells, HepG2 (A), the mouse hepatocyte cell line, FL83B (B), or primary CD-1 mouse hepatocytes (C) were infected with each adenoviral vector from 0 up to 12,500 particles per cell (PPC) of Av3nBg (open circle) or Av3nBgFKO1 (filled circle) for 1 hour at 37C. After 24 hours the cells were fixed and stained with X-gal. The percentage of transduced cells was determined per high-power field for each vector dose. The data represent the mean percentage of transduction ± SD (n = 3 wells) from one representative experiment.

Journal: Molecular therapy : the journal of the American Society of Gene Therapy

Article Title: In vivo hepatic adenoviral gene delivery occurs independently of the coxsackievirus-adenovirus receptor.

doi: 10.1006/mthe.2002.0613

Figure Lengend Snippet: FIG. 7. In vitro adenoviral gene delivery to human and mouse hepatocytes. Human hepatocarcinoma cells, HepG2 (A), the mouse hepatocyte cell line, FL83B (B), or primary CD-1 mouse hepatocytes (C) were infected with each adenoviral vector from 0 up to 12,500 particles per cell (PPC) of Av3nBg (open circle) or Av3nBgFKO1 (filled circle) for 1 hour at 37C. After 24 hours the cells were fixed and stained with X-gal. The percentage of transduced cells was determined per high-power field for each vector dose. The data represent the mean percentage of transduction ± SD (n = 3 wells) from one representative experiment.

Article Snippet: HeLa (human cervical carcinoma; ATCC CCL2), HepG2 (human hepatocarcinoma; ATCC HB-8065), and FL83B, a fetal murine hepatocyte cell line (ATCC CRL-2390), were obtained from the American Type Culture Collection (Manassas, VA), and we cultured each cell line in the recommended medium.

Techniques: In Vitro, Infection, Plasmid Preparation, Staining, Transduction

FIG. 8. Competition analysis of adenoviral transduction of primary murine hepatocytes. CD-1 murine primary hepatocytes were transduced with Av3nBg (wt) at 2500 PPC or Av3nBgFKO1 (KO1) at 12,500 PPC in the presence or absence of fiber knob (10 g/ml), an RGD peptide (200 g/ml), or heparin (3 mg/ml) for 1 hour at 37C. After 24 hours, the cells were fixed and stained with X-gal. The number of transduced cells was determined per high-power field for each condition and was expressed as a percentage of the total trans- duction in the absence of competitor. The level of transduction for each vec- tor in the absence of competitor was defined as 100%. The data show the aver- age percentage control ± SD from a representative experiment.

Journal: Molecular therapy : the journal of the American Society of Gene Therapy

Article Title: In vivo hepatic adenoviral gene delivery occurs independently of the coxsackievirus-adenovirus receptor.

doi: 10.1006/mthe.2002.0613

Figure Lengend Snippet: FIG. 8. Competition analysis of adenoviral transduction of primary murine hepatocytes. CD-1 murine primary hepatocytes were transduced with Av3nBg (wt) at 2500 PPC or Av3nBgFKO1 (KO1) at 12,500 PPC in the presence or absence of fiber knob (10 g/ml), an RGD peptide (200 g/ml), or heparin (3 mg/ml) for 1 hour at 37C. After 24 hours, the cells were fixed and stained with X-gal. The number of transduced cells was determined per high-power field for each condition and was expressed as a percentage of the total trans- duction in the absence of competitor. The level of transduction for each vec- tor in the absence of competitor was defined as 100%. The data show the aver- age percentage control ± SD from a representative experiment.

Article Snippet: HeLa (human cervical carcinoma; ATCC CCL2), HepG2 (human hepatocarcinoma; ATCC HB-8065), and FL83B, a fetal murine hepatocyte cell line (ATCC CRL-2390), were obtained from the American Type Culture Collection (Manassas, VA), and we cultured each cell line in the recommended medium.

Techniques: Transduction, Staining, Control