aml12 atcc atcc cat Search Results


98
ATCC aml12 mouse hepatocytes
Transgene Expression from the miRNA-122- and miRNA-206-Regulated Vectors Is Inhibited in Cell Lines Expressing the Corresponding miRNAs (A) qPCR analysis of relative miRNA-122 expression in different cell lines, normalized to U6 snRNA. Bars represent mean +/- SEM (n = 3-5) Representative western blot analysis of HO-1 protein level in: (B) HEK293 cells 7 days after transduction with scAAV9-HO1 (positive control) or scAAV9-HO1-iTS, and hypoxic conditions (0.5% O 2 ) were applied 24 h before protein isolation; (C) HEK293 cells 7 days after transduction with scAAV9-HO1 (positive control) or scAAV9-HO1-TS, and hypoxic conditions (0.5% O 2 ) were applied 24 h before protein isolation; (D) <t>AML12</t> cells 72 h after transfection with pdAAV-HO-TS or pdAAV-HO1-iTS plasmid; (E) differentiated C2C12 cells 7 days after transduction with scAAV9-HO-TS or scAAV9-HO1-iTS vectors; (F) undifferentiated C2C12 cells 72 h after transfection with pdAAV-HO-TS or pdAAV-HO1-iTS plasmid; and (G) HL-1 cells 72 h after transfection with pdAAV-HO-TS or pdAAV-HO1-iTS plasmid. All experiments were performed in duplicate and were repeated at least three times. In all western blot analyses, α-tubulin served as a loading control.
Aml12 Mouse Hepatocytes, supplied by ATCC, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Dojindo Labs cell counting kit-8
Transgene Expression from the miRNA-122- and miRNA-206-Regulated Vectors Is Inhibited in Cell Lines Expressing the Corresponding miRNAs (A) qPCR analysis of relative miRNA-122 expression in different cell lines, normalized to U6 snRNA. Bars represent mean +/- SEM (n = 3-5) Representative western blot analysis of HO-1 protein level in: (B) HEK293 cells 7 days after transduction with scAAV9-HO1 (positive control) or scAAV9-HO1-iTS, and hypoxic conditions (0.5% O 2 ) were applied 24 h before protein isolation; (C) HEK293 cells 7 days after transduction with scAAV9-HO1 (positive control) or scAAV9-HO1-TS, and hypoxic conditions (0.5% O 2 ) were applied 24 h before protein isolation; (D) <t>AML12</t> cells 72 h after transfection with pdAAV-HO-TS or pdAAV-HO1-iTS plasmid; (E) differentiated C2C12 cells 7 days after transduction with scAAV9-HO-TS or scAAV9-HO1-iTS vectors; (F) undifferentiated C2C12 cells 72 h after transfection with pdAAV-HO-TS or pdAAV-HO1-iTS plasmid; and (G) HL-1 cells 72 h after transfection with pdAAV-HO-TS or pdAAV-HO1-iTS plasmid. All experiments were performed in duplicate and were repeated at least three times. In all western blot analyses, α-tubulin served as a loading control.
Cell Counting Kit 8, supplied by Dojindo Labs, 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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94
ATCC cell lines aml12 mouse hepatocyte cell line atcc cat
Transgene Expression from the miRNA-122- and miRNA-206-Regulated Vectors Is Inhibited in Cell Lines Expressing the Corresponding miRNAs (A) qPCR analysis of relative miRNA-122 expression in different cell lines, normalized to U6 snRNA. Bars represent mean +/- SEM (n = 3-5) Representative western blot analysis of HO-1 protein level in: (B) HEK293 cells 7 days after transduction with scAAV9-HO1 (positive control) or scAAV9-HO1-iTS, and hypoxic conditions (0.5% O 2 ) were applied 24 h before protein isolation; (C) HEK293 cells 7 days after transduction with scAAV9-HO1 (positive control) or scAAV9-HO1-TS, and hypoxic conditions (0.5% O 2 ) were applied 24 h before protein isolation; (D) <t>AML12</t> cells 72 h after transfection with pdAAV-HO-TS or pdAAV-HO1-iTS plasmid; (E) differentiated C2C12 cells 7 days after transduction with scAAV9-HO-TS or scAAV9-HO1-iTS vectors; (F) undifferentiated C2C12 cells 72 h after transfection with pdAAV-HO-TS or pdAAV-HO1-iTS plasmid; and (G) HL-1 cells 72 h after transfection with pdAAV-HO-TS or pdAAV-HO1-iTS plasmid. All experiments were performed in duplicate and were repeated at least three times. In all western blot analyses, α-tubulin served as a loading control.
Cell Lines Aml12 Mouse Hepatocyte Cell Line Atcc Cat, supplied by ATCC, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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94
CLS Cell Lines Service GmbH aml12 cells
Transgene Expression from the miRNA-122- and miRNA-206-Regulated Vectors Is Inhibited in Cell Lines Expressing the Corresponding miRNAs (A) qPCR analysis of relative miRNA-122 expression in different cell lines, normalized to U6 snRNA. Bars represent mean +/- SEM (n = 3-5) Representative western blot analysis of HO-1 protein level in: (B) HEK293 cells 7 days after transduction with scAAV9-HO1 (positive control) or scAAV9-HO1-iTS, and hypoxic conditions (0.5% O 2 ) were applied 24 h before protein isolation; (C) HEK293 cells 7 days after transduction with scAAV9-HO1 (positive control) or scAAV9-HO1-TS, and hypoxic conditions (0.5% O 2 ) were applied 24 h before protein isolation; (D) <t>AML12</t> cells 72 h after transfection with pdAAV-HO-TS or pdAAV-HO1-iTS plasmid; (E) differentiated C2C12 cells 7 days after transduction with scAAV9-HO-TS or scAAV9-HO1-iTS vectors; (F) undifferentiated C2C12 cells 72 h after transfection with pdAAV-HO-TS or pdAAV-HO1-iTS plasmid; and (G) HL-1 cells 72 h after transfection with pdAAV-HO-TS or pdAAV-HO1-iTS plasmid. All experiments were performed in duplicate and were repeated at least three times. In all western blot analyses, α-tubulin served as a loading control.
Aml12 Cells, supplied by CLS Cell Lines Service GmbH, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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86
Procell Inc aml 12
Upregulated hepatocyte-derived IL-25 promotes the formation of METs in liver fibrosis. A qPCR analysis of 31 kinds of Interleukins expression in 4 W LFib mice liver tissues, The heatmap and bar graph visually represent the fold changes of IL-25 and other interleukins. ( n = 6 per group). B qPCR analysis of 31 kinds of Interleukins expression in <t>AML-12,</t> stimulated with culture medium containing 0.2% CCl₄ for 12 h. The heatmap and bar graph visually represent the fold changes of IL-25 and other interleukins. ( n = 6 per group). C Double immunofluorescence staining of mouse liver tissue sections using HNF4α and Il-25 antibodies, with DAPI for nuclear counterstaining with the semi-quantitative results of the processed images from each group, yellow arrows indicate hepatocyte-derived IL-25 (HNF4α⁺Il-25⁺). ( n = 6 per group). Mean ± SEM; * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001. Student’s t-test
Aml 12, supplied by Procell Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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293t  (ATCC)
99
ATCC 293t
Upregulated hepatocyte-derived IL-25 promotes the formation of METs in liver fibrosis. A qPCR analysis of 31 kinds of Interleukins expression in 4 W LFib mice liver tissues, The heatmap and bar graph visually represent the fold changes of IL-25 and other interleukins. ( n = 6 per group). B qPCR analysis of 31 kinds of Interleukins expression in <t>AML-12,</t> stimulated with culture medium containing 0.2% CCl₄ for 12 h. The heatmap and bar graph visually represent the fold changes of IL-25 and other interleukins. ( n = 6 per group). C Double immunofluorescence staining of mouse liver tissue sections using HNF4α and Il-25 antibodies, with DAPI for nuclear counterstaining with the semi-quantitative results of the processed images from each group, yellow arrows indicate hepatocyte-derived IL-25 (HNF4α⁺Il-25⁺). ( n = 6 per group). Mean ± SEM; * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001. Student’s t-test
293t, 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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99
ATCC raw 264.7
Upregulated hepatocyte-derived IL-25 promotes the formation of METs in liver fibrosis. A qPCR analysis of 31 kinds of Interleukins expression in 4 W LFib mice liver tissues, The heatmap and bar graph visually represent the fold changes of IL-25 and other interleukins. ( n = 6 per group). B qPCR analysis of 31 kinds of Interleukins expression in <t>AML-12,</t> stimulated with culture medium containing 0.2% CCl₄ for 12 h. The heatmap and bar graph visually represent the fold changes of IL-25 and other interleukins. ( n = 6 per group). C Double immunofluorescence staining of mouse liver tissue sections using HNF4α and Il-25 antibodies, with DAPI for nuclear counterstaining with the semi-quantitative results of the processed images from each group, yellow arrows indicate hepatocyte-derived IL-25 (HNF4α⁺Il-25⁺). ( n = 6 per group). Mean ± SEM; * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001. Student’s t-test
Raw 264.7, 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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94
CLS Cell Lines Service GmbH hepg2 cells
Upregulated hepatocyte-derived IL-25 promotes the formation of METs in liver fibrosis. A qPCR analysis of 31 kinds of Interleukins expression in 4 W LFib mice liver tissues, The heatmap and bar graph visually represent the fold changes of IL-25 and other interleukins. ( n = 6 per group). B qPCR analysis of 31 kinds of Interleukins expression in <t>AML-12,</t> stimulated with culture medium containing 0.2% CCl₄ for 12 h. The heatmap and bar graph visually represent the fold changes of IL-25 and other interleukins. ( n = 6 per group). C Double immunofluorescence staining of mouse liver tissue sections using HNF4α and Il-25 antibodies, with DAPI for nuclear counterstaining with the semi-quantitative results of the processed images from each group, yellow arrows indicate hepatocyte-derived IL-25 (HNF4α⁺Il-25⁺). ( n = 6 per group). Mean ± SEM; * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001. Student’s t-test
Hepg2 Cells, supplied by CLS Cell Lines Service GmbH, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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99
Dojindo Labs ferroorange
Upregulated hepatocyte-derived IL-25 promotes the formation of METs in liver fibrosis. A qPCR analysis of 31 kinds of Interleukins expression in 4 W LFib mice liver tissues, The heatmap and bar graph visually represent the fold changes of IL-25 and other interleukins. ( n = 6 per group). B qPCR analysis of 31 kinds of Interleukins expression in <t>AML-12,</t> stimulated with culture medium containing 0.2% CCl₄ for 12 h. The heatmap and bar graph visually represent the fold changes of IL-25 and other interleukins. ( n = 6 per group). C Double immunofluorescence staining of mouse liver tissue sections using HNF4α and Il-25 antibodies, with DAPI for nuclear counterstaining with the semi-quantitative results of the processed images from each group, yellow arrows indicate hepatocyte-derived IL-25 (HNF4α⁺Il-25⁺). ( n = 6 per group). Mean ± SEM; * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001. Student’s t-test
Ferroorange, supplied by Dojindo Labs, 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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90
Meridian Bioscience bio-65054
Upregulated hepatocyte-derived IL-25 promotes the formation of METs in liver fibrosis. A qPCR analysis of 31 kinds of Interleukins expression in 4 W LFib mice liver tissues, The heatmap and bar graph visually represent the fold changes of IL-25 and other interleukins. ( n = 6 per group). B qPCR analysis of 31 kinds of Interleukins expression in <t>AML-12,</t> stimulated with culture medium containing 0.2% CCl₄ for 12 h. The heatmap and bar graph visually represent the fold changes of IL-25 and other interleukins. ( n = 6 per group). C Double immunofluorescence staining of mouse liver tissue sections using HNF4α and Il-25 antibodies, with DAPI for nuclear counterstaining with the semi-quantitative results of the processed images from each group, yellow arrows indicate hepatocyte-derived IL-25 (HNF4α⁺Il-25⁺). ( n = 6 per group). Mean ± SEM; * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001. Student’s t-test
Bio 65054, supplied by Meridian Bioscience, 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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90
Pro-cell Co Ltd aml12 (mouse immortalized hepatocytes) (cat number: cl-0007)
Upregulated hepatocyte-derived IL-25 promotes the formation of METs in liver fibrosis. A qPCR analysis of 31 kinds of Interleukins expression in 4 W LFib mice liver tissues, The heatmap and bar graph visually represent the fold changes of IL-25 and other interleukins. ( n = 6 per group). B qPCR analysis of 31 kinds of Interleukins expression in <t>AML-12,</t> stimulated with culture medium containing 0.2% CCl₄ for 12 h. The heatmap and bar graph visually represent the fold changes of IL-25 and other interleukins. ( n = 6 per group). C Double immunofluorescence staining of mouse liver tissue sections using HNF4α and Il-25 antibodies, with DAPI for nuclear counterstaining with the semi-quantitative results of the processed images from each group, yellow arrows indicate hepatocyte-derived IL-25 (HNF4α⁺Il-25⁺). ( n = 6 per group). Mean ± SEM; * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001. Student’s t-test
Aml12 (Mouse Immortalized Hepatocytes) (Cat Number: Cl 0007), supplied by Pro-cell Co Ltd, 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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99
ATCC hepa 1-6
Upregulated hepatocyte-derived IL-25 promotes the formation of METs in liver fibrosis. A qPCR analysis of 31 kinds of Interleukins expression in 4 W LFib mice liver tissues, The heatmap and bar graph visually represent the fold changes of IL-25 and other interleukins. ( n = 6 per group). B qPCR analysis of 31 kinds of Interleukins expression in <t>AML-12,</t> stimulated with culture medium containing 0.2% CCl₄ for 12 h. The heatmap and bar graph visually represent the fold changes of IL-25 and other interleukins. ( n = 6 per group). C Double immunofluorescence staining of mouse liver tissue sections using HNF4α and Il-25 antibodies, with DAPI for nuclear counterstaining with the semi-quantitative results of the processed images from each group, yellow arrows indicate hepatocyte-derived IL-25 (HNF4α⁺Il-25⁺). ( n = 6 per group). Mean ± SEM; * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001. Student’s t-test
Hepa 1 6, 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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Image Search Results


Transgene Expression from the miRNA-122- and miRNA-206-Regulated Vectors Is Inhibited in Cell Lines Expressing the Corresponding miRNAs (A) qPCR analysis of relative miRNA-122 expression in different cell lines, normalized to U6 snRNA. Bars represent mean +/- SEM (n = 3-5) Representative western blot analysis of HO-1 protein level in: (B) HEK293 cells 7 days after transduction with scAAV9-HO1 (positive control) or scAAV9-HO1-iTS, and hypoxic conditions (0.5% O 2 ) were applied 24 h before protein isolation; (C) HEK293 cells 7 days after transduction with scAAV9-HO1 (positive control) or scAAV9-HO1-TS, and hypoxic conditions (0.5% O 2 ) were applied 24 h before protein isolation; (D) AML12 cells 72 h after transfection with pdAAV-HO-TS or pdAAV-HO1-iTS plasmid; (E) differentiated C2C12 cells 7 days after transduction with scAAV9-HO-TS or scAAV9-HO1-iTS vectors; (F) undifferentiated C2C12 cells 72 h after transfection with pdAAV-HO-TS or pdAAV-HO1-iTS plasmid; and (G) HL-1 cells 72 h after transfection with pdAAV-HO-TS or pdAAV-HO1-iTS plasmid. All experiments were performed in duplicate and were repeated at least three times. In all western blot analyses, α-tubulin served as a loading control.

Journal: Molecular Therapy. Methods & Clinical Development

Article Title: Variability in Cardiac miRNA-122 Level Determines Therapeutic Potential of miRNA-Regulated AAV Vectors

doi: 10.1016/j.omtm.2020.05.006

Figure Lengend Snippet: Transgene Expression from the miRNA-122- and miRNA-206-Regulated Vectors Is Inhibited in Cell Lines Expressing the Corresponding miRNAs (A) qPCR analysis of relative miRNA-122 expression in different cell lines, normalized to U6 snRNA. Bars represent mean +/- SEM (n = 3-5) Representative western blot analysis of HO-1 protein level in: (B) HEK293 cells 7 days after transduction with scAAV9-HO1 (positive control) or scAAV9-HO1-iTS, and hypoxic conditions (0.5% O 2 ) were applied 24 h before protein isolation; (C) HEK293 cells 7 days after transduction with scAAV9-HO1 (positive control) or scAAV9-HO1-TS, and hypoxic conditions (0.5% O 2 ) were applied 24 h before protein isolation; (D) AML12 cells 72 h after transfection with pdAAV-HO-TS or pdAAV-HO1-iTS plasmid; (E) differentiated C2C12 cells 7 days after transduction with scAAV9-HO-TS or scAAV9-HO1-iTS vectors; (F) undifferentiated C2C12 cells 72 h after transfection with pdAAV-HO-TS or pdAAV-HO1-iTS plasmid; and (G) HL-1 cells 72 h after transfection with pdAAV-HO-TS or pdAAV-HO1-iTS plasmid. All experiments were performed in duplicate and were repeated at least three times. In all western blot analyses, α-tubulin served as a loading control.

Article Snippet: AML12 mouse hepatocytes (cat. #CRL-2254; ATCC, Manassas, VA, USA) were cultured in DMEM/F12 medium supplemented with 10% FBS and Insulin -Transferrin-Selenium (ITS suplement; ATCC): insulin (0.005 mg/mL), transferrin (0.005 mg/mL), selenium (5 ng/mL), and with dexamethasone (40 ng/mL) in the presence of antibiotics.

Techniques: Expressing, Western Blot, Transduction, Positive Control, Isolation, Transfection, Plasmid Preparation, Control

Upregulated hepatocyte-derived IL-25 promotes the formation of METs in liver fibrosis. A qPCR analysis of 31 kinds of Interleukins expression in 4 W LFib mice liver tissues, The heatmap and bar graph visually represent the fold changes of IL-25 and other interleukins. ( n = 6 per group). B qPCR analysis of 31 kinds of Interleukins expression in AML-12, stimulated with culture medium containing 0.2% CCl₄ for 12 h. The heatmap and bar graph visually represent the fold changes of IL-25 and other interleukins. ( n = 6 per group). C Double immunofluorescence staining of mouse liver tissue sections using HNF4α and Il-25 antibodies, with DAPI for nuclear counterstaining with the semi-quantitative results of the processed images from each group, yellow arrows indicate hepatocyte-derived IL-25 (HNF4α⁺Il-25⁺). ( n = 6 per group). Mean ± SEM; * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001. Student’s t-test

Journal: Inflammation

Article Title: Hepatocyte-Derived IL-25 Promotes Macrophage Extracellular Trap Formation and Drives Liver Fibrosis Progression

doi: 10.1007/s10753-026-02506-6

Figure Lengend Snippet: Upregulated hepatocyte-derived IL-25 promotes the formation of METs in liver fibrosis. A qPCR analysis of 31 kinds of Interleukins expression in 4 W LFib mice liver tissues, The heatmap and bar graph visually represent the fold changes of IL-25 and other interleukins. ( n = 6 per group). B qPCR analysis of 31 kinds of Interleukins expression in AML-12, stimulated with culture medium containing 0.2% CCl₄ for 12 h. The heatmap and bar graph visually represent the fold changes of IL-25 and other interleukins. ( n = 6 per group). C Double immunofluorescence staining of mouse liver tissue sections using HNF4α and Il-25 antibodies, with DAPI for nuclear counterstaining with the semi-quantitative results of the processed images from each group, yellow arrows indicate hepatocyte-derived IL-25 (HNF4α⁺Il-25⁺). ( n = 6 per group). Mean ± SEM; * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001. Student’s t-test

Article Snippet: The murine immortalized macrophage cell line RAW 264.7 (Cat. No. CL-0190, Wuhan, China) and AML-12 (alpha mouse liver 12) cell line was purchased from ProCell (Cat. No. CL-0602, Wuhan, China).

Techniques: Derivative Assay, Expressing, Double Immunofluorescence Staining