normal human lung fibroblast cells Search Results


90
Tibotec Pharmaceuticals human fetal lung-derived normal fibroblast mrc-5 cells
Human Fetal Lung Derived Normal Fibroblast Mrc 5 Cells, supplied by Tibotec Pharmaceuticals, 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/normal+human+lung+fibroblast+cells/us09000194-166-49-17?v=Tibotec+Pharmaceuticals
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human fetal lung-derived normal fibroblast mrc-5 cells - by Bioz Stars, 2026-08
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JCRB Cell Bank human normal lung fibroblasts mrc-5
Human Normal Lung Fibroblasts Mrc 5, supplied by JCRB Cell Bank, 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/normal+human+lung+fibroblast+cells/pmc11394585-60-0-48?v=JCRB+Cell+Bank
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human normal lung fibroblasts mrc-5 - by Bioz Stars, 2026-08
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AddexBio Inc normal human lung fibroblast hel299 cell line
Viability of the normal human lung fibroblast <t>HEL299</t> cells, treated for 48 h with: (a) – free Dox or D- g -PAAan-Dox in Dox-equivalent concentrations, (b) – free Cis or D- g -PAAan-Cis in Cis-equivalent concentrations; * p < 0.05 compared to free drugs.
Normal Human Lung Fibroblast Hel299 Cell Line, supplied by AddexBio 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/normal+human+lung+fibroblast+cells/pmc09680934-183-5-15?v=AddexBio+Inc
Average 90 stars, based on 1 article reviews
normal human lung fibroblast hel299 cell line - by Bioz Stars, 2026-08
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JCRB Cell Bank normal human lung fibroblast cells
Viability of the normal human lung fibroblast <t>HEL299</t> cells, treated for 48 h with: (a) – free Dox or D- g -PAAan-Dox in Dox-equivalent concentrations, (b) – free Cis or D- g -PAAan-Cis in Cis-equivalent concentrations; * p < 0.05 compared to free drugs.
Normal Human Lung Fibroblast Cells, supplied by JCRB Cell Bank, 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/normal+human+lung+fibroblast+cells/10__1016_slash_j__carpta__2021__100115-106-27-33?v=JCRB+Cell+Bank
Average 90 stars, based on 1 article reviews
normal human lung fibroblast cells - by Bioz Stars, 2026-08
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JCRB Cell Bank normal human lung fibroblasts
Type III IFN receptor expression in human gingival keratinocytes. A : Detection of IL10R2 , IFNLR1 , and GAPDH mRNA in various keratinocytes and <t>fibroblasts</t> with (+) or without (-) cDNA by RT-PCR. M, marker. B : Quantitative analysis of IFNLR1 mRNA expression by real-time PCR in various keratinocytes and fibroblasts. Data represent the mean ± standard deviation (SD) of triplicate assays. C : Detection of cell surface IFN-λR1 by flow cytometry. The black line represents IFN-λR1, and the gray area shows the isotype control. A representative histogram from three independent experiments is shown. Values are the mean fluorescence intensity of IFN-λR1 expression and shown as a fold increase in IFN-λR1 expression from that with the control. D : HGK were treated with the indicated concentrations of IFN-λ1 for 30 min. Whole-cell lysates prepared from these cells were immunoblotted with anti-phospho-STAT1 (pSTAT1), anti-STAT1, or anti-GAPDH antibodies. A representative blot is shown. The bar graph shows the integrated signal intensities of the pSTAT1/STAT1 ratio. Data represent the mean ± SD of triplicate assays. * P < 0.05 and ** P < 0.01 versus untreated cells (0) (Dunnett’s multiple comparison test). E : Human gingival sections were stained with an isotype and anti-IFN-λR1 antibody. Sections were counterstained with hematoxylin. Representative images of 3 samples each are shown. The right image is a high-magnification image of the square area. A-D : Data show a representative of at least three independent experiments. OBA-9; an immortalized human gingival keratinocyte cell line. HGK; human primary gingival keratinocytes. HaCaT; an immortalized human skin keratinocyte cell line. HEK; human primary epidermal keratinocytes. HGF; human primary gingival fibroblasts. HFL-III; normal human lung fibroblasts.
Normal Human Lung Fibroblasts, supplied by JCRB Cell Bank, 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/normal+human+lung+fibroblast+cells/pmc08767043-27-0-8?v=JCRB+Cell+Bank
Average 90 stars, based on 1 article reviews
normal human lung fibroblasts - by Bioz Stars, 2026-08
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ScienCell normal endothelial, epithelial, fibroblast, and smooth muscle human primary lung cells
Type III IFN receptor expression in human gingival keratinocytes. A : Detection of IL10R2 , IFNLR1 , and GAPDH mRNA in various keratinocytes and <t>fibroblasts</t> with (+) or without (-) cDNA by RT-PCR. M, marker. B : Quantitative analysis of IFNLR1 mRNA expression by real-time PCR in various keratinocytes and fibroblasts. Data represent the mean ± standard deviation (SD) of triplicate assays. C : Detection of cell surface IFN-λR1 by flow cytometry. The black line represents IFN-λR1, and the gray area shows the isotype control. A representative histogram from three independent experiments is shown. Values are the mean fluorescence intensity of IFN-λR1 expression and shown as a fold increase in IFN-λR1 expression from that with the control. D : HGK were treated with the indicated concentrations of IFN-λ1 for 30 min. Whole-cell lysates prepared from these cells were immunoblotted with anti-phospho-STAT1 (pSTAT1), anti-STAT1, or anti-GAPDH antibodies. A representative blot is shown. The bar graph shows the integrated signal intensities of the pSTAT1/STAT1 ratio. Data represent the mean ± SD of triplicate assays. * P < 0.05 and ** P < 0.01 versus untreated cells (0) (Dunnett’s multiple comparison test). E : Human gingival sections were stained with an isotype and anti-IFN-λR1 antibody. Sections were counterstained with hematoxylin. Representative images of 3 samples each are shown. The right image is a high-magnification image of the square area. A-D : Data show a representative of at least three independent experiments. OBA-9; an immortalized human gingival keratinocyte cell line. HGK; human primary gingival keratinocytes. HaCaT; an immortalized human skin keratinocyte cell line. HEK; human primary epidermal keratinocytes. HGF; human primary gingival fibroblasts. HFL-III; normal human lung fibroblasts.
Normal Endothelial, Epithelial, Fibroblast, And Smooth Muscle Human Primary Lung Cells, supplied by ScienCell, 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/normal+human+lung+fibroblast+cells/10__1016_slash_j__bpj__2010__12__2200-23-6-14?v=ScienCell
Average 90 stars, based on 1 article reviews
normal endothelial, epithelial, fibroblast, and smooth muscle human primary lung cells - by Bioz Stars, 2026-08
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JCRB Cell Bank normal human lung fibroblasts hfliii
Type III IFN receptor expression in human gingival keratinocytes. A : Detection of IL10R2 , IFNLR1 , and GAPDH mRNA in various keratinocytes and <t>fibroblasts</t> with (+) or without (-) cDNA by RT-PCR. M, marker. B : Quantitative analysis of IFNLR1 mRNA expression by real-time PCR in various keratinocytes and fibroblasts. Data represent the mean ± standard deviation (SD) of triplicate assays. C : Detection of cell surface IFN-λR1 by flow cytometry. The black line represents IFN-λR1, and the gray area shows the isotype control. A representative histogram from three independent experiments is shown. Values are the mean fluorescence intensity of IFN-λR1 expression and shown as a fold increase in IFN-λR1 expression from that with the control. D : HGK were treated with the indicated concentrations of IFN-λ1 for 30 min. Whole-cell lysates prepared from these cells were immunoblotted with anti-phospho-STAT1 (pSTAT1), anti-STAT1, or anti-GAPDH antibodies. A representative blot is shown. The bar graph shows the integrated signal intensities of the pSTAT1/STAT1 ratio. Data represent the mean ± SD of triplicate assays. * P < 0.05 and ** P < 0.01 versus untreated cells (0) (Dunnett’s multiple comparison test). E : Human gingival sections were stained with an isotype and anti-IFN-λR1 antibody. Sections were counterstained with hematoxylin. Representative images of 3 samples each are shown. The right image is a high-magnification image of the square area. A-D : Data show a representative of at least three independent experiments. OBA-9; an immortalized human gingival keratinocyte cell line. HGK; human primary gingival keratinocytes. HaCaT; an immortalized human skin keratinocyte cell line. HEK; human primary epidermal keratinocytes. HGF; human primary gingival fibroblasts. HFL-III; normal human lung fibroblasts.
Normal Human Lung Fibroblasts Hfliii, supplied by JCRB Cell Bank, 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/normal+human+lung+fibroblast+cells/10__1074_slash_jbc__m112__446351-71-21-30?v=JCRB+Cell+Bank
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normal human lung fibroblasts hfliii - by Bioz Stars, 2026-08
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JCRB Cell Bank normal human lung fibroblasts hfl-iii
Type III IFN receptor expression in human gingival keratinocytes. A : Detection of IL10R2 , IFNLR1 , and GAPDH mRNA in various keratinocytes and <t>fibroblasts</t> with (+) or without (-) cDNA by RT-PCR. M, marker. B : Quantitative analysis of IFNLR1 mRNA expression by real-time PCR in various keratinocytes and fibroblasts. Data represent the mean ± standard deviation (SD) of triplicate assays. C : Detection of cell surface IFN-λR1 by flow cytometry. The black line represents IFN-λR1, and the gray area shows the isotype control. A representative histogram from three independent experiments is shown. Values are the mean fluorescence intensity of IFN-λR1 expression and shown as a fold increase in IFN-λR1 expression from that with the control. D : HGK were treated with the indicated concentrations of IFN-λ1 for 30 min. Whole-cell lysates prepared from these cells were immunoblotted with anti-phospho-STAT1 (pSTAT1), anti-STAT1, or anti-GAPDH antibodies. A representative blot is shown. The bar graph shows the integrated signal intensities of the pSTAT1/STAT1 ratio. Data represent the mean ± SD of triplicate assays. * P < 0.05 and ** P < 0.01 versus untreated cells (0) (Dunnett’s multiple comparison test). E : Human gingival sections were stained with an isotype and anti-IFN-λR1 antibody. Sections were counterstained with hematoxylin. Representative images of 3 samples each are shown. The right image is a high-magnification image of the square area. A-D : Data show a representative of at least three independent experiments. OBA-9; an immortalized human gingival keratinocyte cell line. HGK; human primary gingival keratinocytes. HaCaT; an immortalized human skin keratinocyte cell line. HEK; human primary epidermal keratinocytes. HGF; human primary gingival fibroblasts. HFL-III; normal human lung fibroblasts.
Normal Human Lung Fibroblasts Hfl Iii, supplied by JCRB Cell Bank, 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/normal+human+lung+fibroblast+cells/pm25921577-70-0-9?v=JCRB+Cell+Bank
Average 90 stars, based on 1 article reviews
normal human lung fibroblasts hfl-iii - by Bioz Stars, 2026-08
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HiMedia Laboratories human normal lung fibroblast (imr90) cell line
Type III IFN receptor expression in human gingival keratinocytes. A : Detection of IL10R2 , IFNLR1 , and GAPDH mRNA in various keratinocytes and <t>fibroblasts</t> with (+) or without (-) cDNA by RT-PCR. M, marker. B : Quantitative analysis of IFNLR1 mRNA expression by real-time PCR in various keratinocytes and fibroblasts. Data represent the mean ± standard deviation (SD) of triplicate assays. C : Detection of cell surface IFN-λR1 by flow cytometry. The black line represents IFN-λR1, and the gray area shows the isotype control. A representative histogram from three independent experiments is shown. Values are the mean fluorescence intensity of IFN-λR1 expression and shown as a fold increase in IFN-λR1 expression from that with the control. D : HGK were treated with the indicated concentrations of IFN-λ1 for 30 min. Whole-cell lysates prepared from these cells were immunoblotted with anti-phospho-STAT1 (pSTAT1), anti-STAT1, or anti-GAPDH antibodies. A representative blot is shown. The bar graph shows the integrated signal intensities of the pSTAT1/STAT1 ratio. Data represent the mean ± SD of triplicate assays. * P < 0.05 and ** P < 0.01 versus untreated cells (0) (Dunnett’s multiple comparison test). E : Human gingival sections were stained with an isotype and anti-IFN-λR1 antibody. Sections were counterstained with hematoxylin. Representative images of 3 samples each are shown. The right image is a high-magnification image of the square area. A-D : Data show a representative of at least three independent experiments. OBA-9; an immortalized human gingival keratinocyte cell line. HGK; human primary gingival keratinocytes. HaCaT; an immortalized human skin keratinocyte cell line. HEK; human primary epidermal keratinocytes. HGF; human primary gingival fibroblasts. HFL-III; normal human lung fibroblasts.
Human Normal Lung Fibroblast (Imr90) Cell Line, supplied by HiMedia Laboratories, 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/normal+human+lung+fibroblast+cells/pm37004322-63-2-13?v=HiMedia+Laboratories
Average 90 stars, based on 1 article reviews
human normal lung fibroblast (imr90) cell line - by Bioz Stars, 2026-08
90/100 stars
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Image Search Results


Viability of the normal human lung fibroblast HEL299 cells, treated for 48 h with: (a) – free Dox or D- g -PAAan-Dox in Dox-equivalent concentrations, (b) – free Cis or D- g -PAAan-Cis in Cis-equivalent concentrations; * p < 0.05 compared to free drugs.

Journal: Nanoscale Advances

Article Title: Drug delivery with a pH-sensitive star-like dextran-graft polyacrylamide copolymer

doi: 10.1039/d2na00353h

Figure Lengend Snippet: Viability of the normal human lung fibroblast HEL299 cells, treated for 48 h with: (a) – free Dox or D- g -PAAan-Dox in Dox-equivalent concentrations, (b) – free Cis or D- g -PAAan-Cis in Cis-equivalent concentrations; * p < 0.05 compared to free drugs.

Article Snippet: Lung carcinoma human A549 and normal human lung fibroblast HEL299 cell lines were purchased from AddexBio Technologies (San Diego, CA, USA).

Techniques:

IC 50 of free drugs and drug-loaded D- g -PAAan nanoparticles on  HEL299  cell viability

Journal: Nanoscale Advances

Article Title: Drug delivery with a pH-sensitive star-like dextran-graft polyacrylamide copolymer

doi: 10.1039/d2na00353h

Figure Lengend Snippet: IC 50 of free drugs and drug-loaded D- g -PAAan nanoparticles on HEL299 cell viability

Article Snippet: Lung carcinoma human A549 and normal human lung fibroblast HEL299 cell lines were purchased from AddexBio Technologies (San Diego, CA, USA).

Techniques:

Type III IFN receptor expression in human gingival keratinocytes. A : Detection of IL10R2 , IFNLR1 , and GAPDH mRNA in various keratinocytes and fibroblasts with (+) or without (-) cDNA by RT-PCR. M, marker. B : Quantitative analysis of IFNLR1 mRNA expression by real-time PCR in various keratinocytes and fibroblasts. Data represent the mean ± standard deviation (SD) of triplicate assays. C : Detection of cell surface IFN-λR1 by flow cytometry. The black line represents IFN-λR1, and the gray area shows the isotype control. A representative histogram from three independent experiments is shown. Values are the mean fluorescence intensity of IFN-λR1 expression and shown as a fold increase in IFN-λR1 expression from that with the control. D : HGK were treated with the indicated concentrations of IFN-λ1 for 30 min. Whole-cell lysates prepared from these cells were immunoblotted with anti-phospho-STAT1 (pSTAT1), anti-STAT1, or anti-GAPDH antibodies. A representative blot is shown. The bar graph shows the integrated signal intensities of the pSTAT1/STAT1 ratio. Data represent the mean ± SD of triplicate assays. * P < 0.05 and ** P < 0.01 versus untreated cells (0) (Dunnett’s multiple comparison test). E : Human gingival sections were stained with an isotype and anti-IFN-λR1 antibody. Sections were counterstained with hematoxylin. Representative images of 3 samples each are shown. The right image is a high-magnification image of the square area. A-D : Data show a representative of at least three independent experiments. OBA-9; an immortalized human gingival keratinocyte cell line. HGK; human primary gingival keratinocytes. HaCaT; an immortalized human skin keratinocyte cell line. HEK; human primary epidermal keratinocytes. HGF; human primary gingival fibroblasts. HFL-III; normal human lung fibroblasts.

Journal: Inflammation

Article Title: The Priming Potential of Interferon Lambda-1 for Antiviral Defense in the Oral Mucosa

doi: 10.1007/s10753-022-01624-1

Figure Lengend Snippet: Type III IFN receptor expression in human gingival keratinocytes. A : Detection of IL10R2 , IFNLR1 , and GAPDH mRNA in various keratinocytes and fibroblasts with (+) or without (-) cDNA by RT-PCR. M, marker. B : Quantitative analysis of IFNLR1 mRNA expression by real-time PCR in various keratinocytes and fibroblasts. Data represent the mean ± standard deviation (SD) of triplicate assays. C : Detection of cell surface IFN-λR1 by flow cytometry. The black line represents IFN-λR1, and the gray area shows the isotype control. A representative histogram from three independent experiments is shown. Values are the mean fluorescence intensity of IFN-λR1 expression and shown as a fold increase in IFN-λR1 expression from that with the control. D : HGK were treated with the indicated concentrations of IFN-λ1 for 30 min. Whole-cell lysates prepared from these cells were immunoblotted with anti-phospho-STAT1 (pSTAT1), anti-STAT1, or anti-GAPDH antibodies. A representative blot is shown. The bar graph shows the integrated signal intensities of the pSTAT1/STAT1 ratio. Data represent the mean ± SD of triplicate assays. * P < 0.05 and ** P < 0.01 versus untreated cells (0) (Dunnett’s multiple comparison test). E : Human gingival sections were stained with an isotype and anti-IFN-λR1 antibody. Sections were counterstained with hematoxylin. Representative images of 3 samples each are shown. The right image is a high-magnification image of the square area. A-D : Data show a representative of at least three independent experiments. OBA-9; an immortalized human gingival keratinocyte cell line. HGK; human primary gingival keratinocytes. HaCaT; an immortalized human skin keratinocyte cell line. HEK; human primary epidermal keratinocytes. HGF; human primary gingival fibroblasts. HFL-III; normal human lung fibroblasts.

Article Snippet: Normal human lung fibroblasts were provided by the Japanese Collection of Research Bioresources Cell Bank.

Techniques: Expressing, Reverse Transcription Polymerase Chain Reaction, Marker, Real-time Polymerase Chain Reaction, Standard Deviation, Flow Cytometry, Control, Fluorescence, Comparison, Staining