murine normal hepatocyte cell line bnl cl Search Results


murine normal hepatocytes  (ATCC)
99
ATCC murine normal hepatocytes
Murine Normal Hepatocytes, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 99 stars, based on 1 article reviews
murine normal hepatocytes - by Bioz Stars, 2026-02
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gene exp pcbd1 mm00481144 m1  (Thermo Fisher)
91
Thermo Fisher gene exp pcbd1 mm00481144 m1
Gene Exp Pcbd1 Mm00481144 M1, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/gene exp pcbd1 mm00481144 m1/product/Thermo Fisher
Average 91 stars, based on 1 article reviews
gene exp pcbd1 mm00481144 m1 - by Bioz Stars, 2026-02
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murine normal hepatocyte line aml12  (Cyagen Biosciences)
90
Cyagen Biosciences murine normal hepatocyte line aml12
(A–E) APOA4 , PCSK9 , HMGCR, ABCG5 , and ABCG8 mRNA expression levels in TMAO-treated and control <t>AML12</t> cells (n = 3 per group). (F) Immunofluorescence staining for APOA4, PCSK9, HMGCR, ABCG5, and ABCG8 in cells from each group. ** p < 0.01, *** p < 0.001. TMAO, trimethylamine-N-oxide; APOA4, apolipoprotein A4; PCSK9, proprotein convertase subtilisin/kexin type 9; ABCG5, ATP-binding cassette sub-family G member 5; ABCG8, ATP-binding cassette sub-family G member 8; HMGCR, 3-hydroxy-3-methylglutaryl-CoA reductase.
Murine Normal Hepatocyte Line Aml12, supplied by Cyagen Biosciences, 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/result/murine normal hepatocyte line aml12/product/Cyagen Biosciences
Average 90 stars, based on 1 article reviews
murine normal hepatocyte line aml12 - by Bioz Stars, 2026-02
90/100 stars
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murine normal hepatocyte fl83b  (BioResource International Inc)
90
BioResource International Inc murine normal hepatocyte fl83b
Cytotoxicity of PG/Dox against normal cells. <t>FL83B,</t> HK-2, and h9c2 cells were sequentially treated with PG/Dox for 12 and 24 h, respectively, and cell viability was measured by MTT assay. Data were represented with mean ± SD from four independent experiments. Columns significantly different letter ( p < 0.05 ) to each other would be labeled with different letters
Murine Normal Hepatocyte 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/result/murine normal hepatocyte fl83b/product/BioResource International Inc
Average 90 stars, based on 1 article reviews
murine normal hepatocyte fl83b - by Bioz Stars, 2026-02
90/100 stars
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murine normal hepatic cell line nctc1469  (China Center for Type Culture Collection)
90
China Center for Type Culture Collection murine normal hepatic cell line nctc1469
Cytotoxicity of PG/Dox against normal cells. <t>FL83B,</t> HK-2, and h9c2 cells were sequentially treated with PG/Dox for 12 and 24 h, respectively, and cell viability was measured by MTT assay. Data were represented with mean ± SD from four independent experiments. Columns significantly different letter ( p < 0.05 ) to each other would be labeled with different letters
Murine Normal Hepatic Cell Line Nctc1469, supplied by China Center for Type Culture Collection, 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/result/murine normal hepatic cell line nctc1469/product/China Center for Type Culture Collection
Average 90 stars, based on 1 article reviews
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murine normal hepatocyte cell line bnl cl  (ATCC)
95
ATCC murine normal hepatocyte cell line bnl cl
Cytotoxicity of PG/Dox against normal cells. <t>FL83B,</t> HK-2, and h9c2 cells were sequentially treated with PG/Dox for 12 and 24 h, respectively, and cell viability was measured by MTT assay. Data were represented with mean ± SD from four independent experiments. Columns significantly different letter ( p < 0.05 ) to each other would be labeled with different letters
Murine Normal Hepatocyte Cell Line Bnl Cl, 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/result/murine normal hepatocyte cell line bnl cl/product/ATCC
Average 95 stars, based on 1 article reviews
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mouse anti–poly(adp-ribose) polymerase monoclonal antibody  (Becton Dickinson)
90
Becton Dickinson mouse anti–poly(adp-ribose) polymerase monoclonal antibody
Cytotoxicity of PG/Dox against normal cells. <t>FL83B,</t> HK-2, and h9c2 cells were sequentially treated with PG/Dox for 12 and 24 h, respectively, and cell viability was measured by MTT assay. Data were represented with mean ± SD from four independent experiments. Columns significantly different letter ( p < 0.05 ) to each other would be labeled with different letters
Mouse Anti–Poly(Adp Ribose) Polymerase Monoclonal Antibody, supplied by Becton Dickinson, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
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Image Search Results


(A–E) APOA4 , PCSK9 , HMGCR, ABCG5 , and ABCG8 mRNA expression levels in TMAO-treated and control AML12 cells (n = 3 per group). (F) Immunofluorescence staining for APOA4, PCSK9, HMGCR, ABCG5, and ABCG8 in cells from each group. ** p < 0.01, *** p < 0.001. TMAO, trimethylamine-N-oxide; APOA4, apolipoprotein A4; PCSK9, proprotein convertase subtilisin/kexin type 9; ABCG5, ATP-binding cassette sub-family G member 5; ABCG8, ATP-binding cassette sub-family G member 8; HMGCR, 3-hydroxy-3-methylglutaryl-CoA reductase.

Journal: Journal of Clinical and Translational Hepatology

Article Title: PCSK9 and APOA4 : The Dynamic Duo in TMAO-induced Cholesterol Metabolism and Cholelithiasis

doi: 10.14218/JCTH.2024.00403

Figure Lengend Snippet: (A–E) APOA4 , PCSK9 , HMGCR, ABCG5 , and ABCG8 mRNA expression levels in TMAO-treated and control AML12 cells (n = 3 per group). (F) Immunofluorescence staining for APOA4, PCSK9, HMGCR, ABCG5, and ABCG8 in cells from each group. ** p < 0.01, *** p < 0.001. TMAO, trimethylamine-N-oxide; APOA4, apolipoprotein A4; PCSK9, proprotein convertase subtilisin/kexin type 9; ABCG5, ATP-binding cassette sub-family G member 5; ABCG8, ATP-binding cassette sub-family G member 8; HMGCR, 3-hydroxy-3-methylglutaryl-CoA reductase.

Article Snippet: The murine normal hepatocyte line AML12 was acquired from Cyagen Biosciences Inc. (Shanghai, China) and cultured using AML12 cell-specific culture medium (Procell, Wuhan).

Techniques: Expressing, Control, Immunofluorescence, Staining, Binding Assay

Cytotoxicity of PG/Dox against normal cells. FL83B, HK-2, and h9c2 cells were sequentially treated with PG/Dox for 12 and 24 h, respectively, and cell viability was measured by MTT assay. Data were represented with mean ± SD from four independent experiments. Columns significantly different letter ( p < 0.05 ) to each other would be labeled with different letters

Journal: Molecular and Cellular Biochemistry

Article Title: Doxorubicin metabolism moderately attributes to putative toxicity in prodigiosin/doxorubicin synergism in vitro cells

doi: 10.1007/s11010-020-03864-x

Figure Lengend Snippet: Cytotoxicity of PG/Dox against normal cells. FL83B, HK-2, and h9c2 cells were sequentially treated with PG/Dox for 12 and 24 h, respectively, and cell viability was measured by MTT assay. Data were represented with mean ± SD from four independent experiments. Columns significantly different letter ( p < 0.05 ) to each other would be labeled with different letters

Article Snippet: A total of 3 cell lines were from different sources: murine normal hepatocyte FL83B and cardio-myoblast h9c2 from Bioresource Collection and Research Center (BCRC, Hsinchu, Taiwan), and human renal cortex/proximal tubule epithelial cell HK-2 from Prof. Yaw-Syan Fu (Department of Biomedical Science and Environment Biology, Kaohsiung Medical University, Kaohsiung, Taiwan) were applied to test the hypothesis in this study.

Techniques: MTT Assay, Labeling

Cytotoxic alteration of PG/Dox by addition of autophagic inhibitors in normal cells. FL83B, HK-2, and h9c2 cells were treated with PG coupled with 3-methyladenine (3MA) or bafilomycin A1 (BA1) for 12 h following by Dox for 12 h, respectively. Results were normalized with untreated control and shown in mean ± SD from four independent experiments. “*” and “#” were represented to significantly different with untreated control and PG/Dox alone, respectively

Journal: Molecular and Cellular Biochemistry

Article Title: Doxorubicin metabolism moderately attributes to putative toxicity in prodigiosin/doxorubicin synergism in vitro cells

doi: 10.1007/s11010-020-03864-x

Figure Lengend Snippet: Cytotoxic alteration of PG/Dox by addition of autophagic inhibitors in normal cells. FL83B, HK-2, and h9c2 cells were treated with PG coupled with 3-methyladenine (3MA) or bafilomycin A1 (BA1) for 12 h following by Dox for 12 h, respectively. Results were normalized with untreated control and shown in mean ± SD from four independent experiments. “*” and “#” were represented to significantly different with untreated control and PG/Dox alone, respectively

Article Snippet: A total of 3 cell lines were from different sources: murine normal hepatocyte FL83B and cardio-myoblast h9c2 from Bioresource Collection and Research Center (BCRC, Hsinchu, Taiwan), and human renal cortex/proximal tubule epithelial cell HK-2 from Prof. Yaw-Syan Fu (Department of Biomedical Science and Environment Biology, Kaohsiung Medical University, Kaohsiung, Taiwan) were applied to test the hypothesis in this study.

Techniques: Control

Cell cycle change in normal cells after PG/Dox treatment. FL83B, HK-2, and h9c2 were treated with PG and Dox, respectively, stained with PI, and determined intracellular fluorescent intensity by flow cytometry. Data were summarized from three independent experiments and shown in mean ± SD which were marked with “*” or “#” as significantly different ( p < 0.05 ) with untreated control or Dox alone

Journal: Molecular and Cellular Biochemistry

Article Title: Doxorubicin metabolism moderately attributes to putative toxicity in prodigiosin/doxorubicin synergism in vitro cells

doi: 10.1007/s11010-020-03864-x

Figure Lengend Snippet: Cell cycle change in normal cells after PG/Dox treatment. FL83B, HK-2, and h9c2 were treated with PG and Dox, respectively, stained with PI, and determined intracellular fluorescent intensity by flow cytometry. Data were summarized from three independent experiments and shown in mean ± SD which were marked with “*” or “#” as significantly different ( p < 0.05 ) with untreated control or Dox alone

Article Snippet: A total of 3 cell lines were from different sources: murine normal hepatocyte FL83B and cardio-myoblast h9c2 from Bioresource Collection and Research Center (BCRC, Hsinchu, Taiwan), and human renal cortex/proximal tubule epithelial cell HK-2 from Prof. Yaw-Syan Fu (Department of Biomedical Science and Environment Biology, Kaohsiung Medical University, Kaohsiung, Taiwan) were applied to test the hypothesis in this study.

Techniques: Staining, Flow Cytometry, Control