primary normal human lung fibroblasts Search Results


95
ATCC primary 489 human embryonic lung fibroblasts
Primary 489 Human Embryonic Lung Fibroblasts, 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
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hlf  (ATCC)
99
ATCC hlf
PXDN and laminin expression are modulated in human lung fibroblasts <t>(HLF)</t> and bone-marrow-derived macrophages (BMDM) upon TGF-β1 stimulation. (A – C) HLFs were treated 5 ng/mL TGF-β1 for 48 h, and analyzed for LAMA1 (A) or PXDN (B) mRNA or PXDN protein expression (C). (D – G) BMDM from C57BL6/NJ mice were treated 5 ng/mL TGF-β1 for 48 h, and analyzed for Pxdn (D) , Lama1 (E) , or Lamb1 (F) mRNA, or Laminin α/β1 protein expression by immunofluorescence imaging (G). Scale bar: 50 μm. Values are the mean of at least three independent biological replicates ± SEM. Differences among groups were evaluated by Student's T-test.
Hlf, 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
hlf - by Bioz Stars, 2025-02
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94
ATCC human lung fibroblasts
PXDN and laminin expression are modulated in human lung fibroblasts <t>(HLF)</t> and bone-marrow-derived macrophages (BMDM) upon TGF-β1 stimulation. (A – C) HLFs were treated 5 ng/mL TGF-β1 for 48 h, and analyzed for LAMA1 (A) or PXDN (B) mRNA or PXDN protein expression (C). (D – G) BMDM from C57BL6/NJ mice were treated 5 ng/mL TGF-β1 for 48 h, and analyzed for Pxdn (D) , Lama1 (E) , or Lamb1 (F) mRNA, or Laminin α/β1 protein expression by immunofluorescence imaging (G). Scale bar: 50 μm. Values are the mean of at least three independent biological replicates ± SEM. Differences among groups were evaluated by Student's T-test.
Human Lung Fibroblasts, 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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Average 94 stars, based on 1 article reviews
human lung fibroblasts - by Bioz Stars, 2025-02
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96
ATCC primary fetal lung cell line hfl 1
PXDN and laminin expression are modulated in human lung fibroblasts <t>(HLF)</t> and bone-marrow-derived macrophages (BMDM) upon TGF-β1 stimulation. (A – C) HLFs were treated 5 ng/mL TGF-β1 for 48 h, and analyzed for LAMA1 (A) or PXDN (B) mRNA or PXDN protein expression (C). (D – G) BMDM from C57BL6/NJ mice were treated 5 ng/mL TGF-β1 for 48 h, and analyzed for Pxdn (D) , Lama1 (E) , or Lamb1 (F) mRNA, or Laminin α/β1 protein expression by immunofluorescence imaging (G). Scale bar: 50 μm. Values are the mean of at least three independent biological replicates ± SEM. Differences among groups were evaluated by Student's T-test.
Primary Fetal Lung Cell Line Hfl 1, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 96 stars, based on 1 article reviews
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98
ATCC imr90 human primary lung embryo fibroblasts
Small e1a causes global deacetylation and redistribution of H3K18ac. ( A ) Venn diagram showing the overlap between significant peaks of H3K18ac in mock- (dark blue) and dl 1500-infected cells (light blue). ( B ) Venn diagram showing the overlap between significant peaks of H3K9ac in mock- (dark orange) and dl 1500-infected cells (yellow). ( C ) Patterns of H3K18ac and H3K9ac in the intergenic region between COPS8 and COL6A3 genes in mock-, dl 1500-infected, and asynchronous <t>IMR90</t> cells. ( D ) Quantitative PCR (% of input) for EP300 and CREBBP in mock- and dl 1500-infected cells for the COL6A3 intergenic region, and CCNE2 and POLD3 promoters are shown as bar plots. Patterns of H3K18ac in mock- and dl 1500-infected cells at CCNE2 and POLD3 loci are also shown. For each histone modification, the y -axis indicates the number of input-normalized ChIP-seq reads across the locus ( x -axis). (Light blue arrows) New peaks of acetylation in e1a-expressing cells. (Dark arrows) Direction of transcription. ( E , F ) Overview of distribution of H3K18ac and H3K9ac peaks in mock- and dl 1500-infected cells in relation to gene structure are shown as pie charts. ( G ) Distribution of significant peaks of H3K18ac with respect to TSS in mock- (dark blue) and dl 1500-infected (light blue) cells. ( H ) Distribution of significant peaks of H3K9ac with respect to TSS in mock- (dark orange) and dl 1500-infected (yellow) cells.
Imr90 Human Primary Lung Embryo Fibroblasts, 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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Average 98 stars, based on 1 article reviews
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Image Search Results


PXDN and laminin expression are modulated in human lung fibroblasts (HLF) and bone-marrow-derived macrophages (BMDM) upon TGF-β1 stimulation. (A – C) HLFs were treated 5 ng/mL TGF-β1 for 48 h, and analyzed for LAMA1 (A) or PXDN (B) mRNA or PXDN protein expression (C). (D – G) BMDM from C57BL6/NJ mice were treated 5 ng/mL TGF-β1 for 48 h, and analyzed for Pxdn (D) , Lama1 (E) , or Lamb1 (F) mRNA, or Laminin α/β1 protein expression by immunofluorescence imaging (G). Scale bar: 50 μm. Values are the mean of at least three independent biological replicates ± SEM. Differences among groups were evaluated by Student's T-test.

Journal: Redox Biology

Article Title: Identification of tyrosine brominated extracellular matrix proteins in normal and fibrotic lung tissues

doi: 10.1016/j.redox.2024.103102

Figure Lengend Snippet: PXDN and laminin expression are modulated in human lung fibroblasts (HLF) and bone-marrow-derived macrophages (BMDM) upon TGF-β1 stimulation. (A – C) HLFs were treated 5 ng/mL TGF-β1 for 48 h, and analyzed for LAMA1 (A) or PXDN (B) mRNA or PXDN protein expression (C). (D – G) BMDM from C57BL6/NJ mice were treated 5 ng/mL TGF-β1 for 48 h, and analyzed for Pxdn (D) , Lama1 (E) , or Lamb1 (F) mRNA, or Laminin α/β1 protein expression by immunofluorescence imaging (G). Scale bar: 50 μm. Values are the mean of at least three independent biological replicates ± SEM. Differences among groups were evaluated by Student's T-test.

Article Snippet: HLF (ATCC PCS-201-013) were cultured in fibroblast basal medium (ATCC PCS-201-030) with fibroblast growth kit-low serum (ATCC PCS-201-041) at 37 °C in a 5% CO 2 atmosphere.

Techniques: Expressing, Derivative Assay, Immunofluorescence, Imaging

Small e1a causes global deacetylation and redistribution of H3K18ac. ( A ) Venn diagram showing the overlap between significant peaks of H3K18ac in mock- (dark blue) and dl 1500-infected cells (light blue). ( B ) Venn diagram showing the overlap between significant peaks of H3K9ac in mock- (dark orange) and dl 1500-infected cells (yellow). ( C ) Patterns of H3K18ac and H3K9ac in the intergenic region between COPS8 and COL6A3 genes in mock-, dl 1500-infected, and asynchronous IMR90 cells. ( D ) Quantitative PCR (% of input) for EP300 and CREBBP in mock- and dl 1500-infected cells for the COL6A3 intergenic region, and CCNE2 and POLD3 promoters are shown as bar plots. Patterns of H3K18ac in mock- and dl 1500-infected cells at CCNE2 and POLD3 loci are also shown. For each histone modification, the y -axis indicates the number of input-normalized ChIP-seq reads across the locus ( x -axis). (Light blue arrows) New peaks of acetylation in e1a-expressing cells. (Dark arrows) Direction of transcription. ( E , F ) Overview of distribution of H3K18ac and H3K9ac peaks in mock- and dl 1500-infected cells in relation to gene structure are shown as pie charts. ( G ) Distribution of significant peaks of H3K18ac with respect to TSS in mock- (dark blue) and dl 1500-infected (light blue) cells. ( H ) Distribution of significant peaks of H3K9ac with respect to TSS in mock- (dark orange) and dl 1500-infected (yellow) cells.

Journal: Genome Research

Article Title: Reorganization of the host epigenome by a viral oncogene

doi: 10.1101/gr.132308.111

Figure Lengend Snippet: Small e1a causes global deacetylation and redistribution of H3K18ac. ( A ) Venn diagram showing the overlap between significant peaks of H3K18ac in mock- (dark blue) and dl 1500-infected cells (light blue). ( B ) Venn diagram showing the overlap between significant peaks of H3K9ac in mock- (dark orange) and dl 1500-infected cells (yellow). ( C ) Patterns of H3K18ac and H3K9ac in the intergenic region between COPS8 and COL6A3 genes in mock-, dl 1500-infected, and asynchronous IMR90 cells. ( D ) Quantitative PCR (% of input) for EP300 and CREBBP in mock- and dl 1500-infected cells for the COL6A3 intergenic region, and CCNE2 and POLD3 promoters are shown as bar plots. Patterns of H3K18ac in mock- and dl 1500-infected cells at CCNE2 and POLD3 loci are also shown. For each histone modification, the y -axis indicates the number of input-normalized ChIP-seq reads across the locus ( x -axis). (Light blue arrows) New peaks of acetylation in e1a-expressing cells. (Dark arrows) Direction of transcription. ( E , F ) Overview of distribution of H3K18ac and H3K9ac peaks in mock- and dl 1500-infected cells in relation to gene structure are shown as pie charts. ( G ) Distribution of significant peaks of H3K18ac with respect to TSS in mock- (dark blue) and dl 1500-infected (light blue) cells. ( H ) Distribution of significant peaks of H3K9ac with respect to TSS in mock- (dark orange) and dl 1500-infected (yellow) cells.

Article Snippet: IMR90 human primary lung embryo fibroblasts (ATCC) were grown in Dulbecco's modified Eagle's medium (DMEM) supplemented with 100 U/mL penicillin, 100 μg/mL streptomycin, and 10% fetal bovine serum (FBS) at 37°C in 5% CO 2 .

Techniques: Infection, Real-time Polymerase Chain Reaction, Modification, ChIP-sequencing, Expressing

Analyses of RB-family protein genome-wide binding in contact-inhibited IMR90 fibroblasts. ( A ) Overview of RB1, RBL2, and RBL1 peak distributions in mock-infected cells in relation to gene structure are shown as pie charts. ( B ) Average binding profiles (significant counts) of the indicated RB-family members across the TSS regions of their respective target genes. ( C ) A 600-bp region around the peaks of RB1, RBL2, and RBL1 in mock-infected cells were analyzed for TF binding motifs using sitepro (Galaxy). Top three significant motifs for each family member are shown. All P -values are less than 1 × 10 −10 . ( D ) The distributions of the RB-family proteins across ±5 kb of TSS for genes with at least one RB-family member bound are shown as heat maps. The seven clusters are based on combinatorial binding patterns of the three proteins. ( E ) Relative gene expression changes of each of the seven clusters after e1a expression at 24 h p.i. are shown as box plots.

Journal: Genome Research

Article Title: Reorganization of the host epigenome by a viral oncogene

doi: 10.1101/gr.132308.111

Figure Lengend Snippet: Analyses of RB-family protein genome-wide binding in contact-inhibited IMR90 fibroblasts. ( A ) Overview of RB1, RBL2, and RBL1 peak distributions in mock-infected cells in relation to gene structure are shown as pie charts. ( B ) Average binding profiles (significant counts) of the indicated RB-family members across the TSS regions of their respective target genes. ( C ) A 600-bp region around the peaks of RB1, RBL2, and RBL1 in mock-infected cells were analyzed for TF binding motifs using sitepro (Galaxy). Top three significant motifs for each family member are shown. All P -values are less than 1 × 10 −10 . ( D ) The distributions of the RB-family proteins across ±5 kb of TSS for genes with at least one RB-family member bound are shown as heat maps. The seven clusters are based on combinatorial binding patterns of the three proteins. ( E ) Relative gene expression changes of each of the seven clusters after e1a expression at 24 h p.i. are shown as box plots.

Article Snippet: IMR90 human primary lung embryo fibroblasts (ATCC) were grown in Dulbecco's modified Eagle's medium (DMEM) supplemented with 100 U/mL penicillin, 100 μg/mL streptomycin, and 10% fetal bovine serum (FBS) at 37°C in 5% CO 2 .

Techniques: Genome Wide, Binding Assay, Infection, Expressing