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ATCC human dermal fibroblast hdf cells
Human Dermal Fibroblast Hdf Cells, 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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PromoCell normal human dermal fibroblasts hdfs
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Cell Applications Inc human dermal fibroblasts hdf
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Pasteur Institute hdf adult primary dermal fibroblast line
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hdfs  (ATCC)
99
ATCC hdfs
Isolation and characterization of chorionic plate mesenchymal stem cell (CP-MSC)-derived sEVs. (A) Schematic showing the isolation and characterization of sEVs derived from <t>CP-MSCs</t> <t>cultured</t> under O₂ Nor , O₂ Hypo-5% , or O₂ Hypo-3% conditions. (B) TEM images showing the typical bilayer structure of sEVs Nor , sEVs Hypo-5% , and sEVs Hypo-3% ; scale bar = 100 nm. (C) Nanoparticle tracking analysis (NTA) profiles showing the size distribution and concentration of sEVs Nor , sEVs Hypo-5% , and sEVs Hypo-3% after 400-fold dilution. (D) Western blotting analysis showing the expression of CD9, CD63, TSG101, and Calnexin proteins in these 3 sEVs. (E) Confocal microscopy images showing the internalization of Dil-labeled sEVs by high-glucose human umbilical vein endothelial cells (HG-HUVECs) and high-glucose human dermal fibroblasts <t>(HG-HDFs);</t> scale bar = 100 μm.
Hdfs, 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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ATCC primary hdf
Isolation and characterization of chorionic plate mesenchymal stem cell (CP-MSC)-derived sEVs. (A) Schematic showing the isolation and characterization of sEVs derived from <t>CP-MSCs</t> <t>cultured</t> under O₂ Nor , O₂ Hypo-5% , or O₂ Hypo-3% conditions. (B) TEM images showing the typical bilayer structure of sEVs Nor , sEVs Hypo-5% , and sEVs Hypo-3% ; scale bar = 100 nm. (C) Nanoparticle tracking analysis (NTA) profiles showing the size distribution and concentration of sEVs Nor , sEVs Hypo-5% , and sEVs Hypo-3% after 400-fold dilution. (D) Western blotting analysis showing the expression of CD9, CD63, TSG101, and Calnexin proteins in these 3 sEVs. (E) Confocal microscopy images showing the internalization of Dil-labeled sEVs by high-glucose human umbilical vein endothelial cells (HG-HUVECs) and high-glucose human dermal fibroblasts <t>(HG-HDFs);</t> scale bar = 100 μm.
Primary Hdf, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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86
Korean Cell Line Bank primary human dermal fibroblast hdf cells
Isolation and characterization of chorionic plate mesenchymal stem cell (CP-MSC)-derived sEVs. (A) Schematic showing the isolation and characterization of sEVs derived from <t>CP-MSCs</t> <t>cultured</t> under O₂ Nor , O₂ Hypo-5% , or O₂ Hypo-3% conditions. (B) TEM images showing the typical bilayer structure of sEVs Nor , sEVs Hypo-5% , and sEVs Hypo-3% ; scale bar = 100 nm. (C) Nanoparticle tracking analysis (NTA) profiles showing the size distribution and concentration of sEVs Nor , sEVs Hypo-5% , and sEVs Hypo-3% after 400-fold dilution. (D) Western blotting analysis showing the expression of CD9, CD63, TSG101, and Calnexin proteins in these 3 sEVs. (E) Confocal microscopy images showing the internalization of Dil-labeled sEVs by high-glucose human umbilical vein endothelial cells (HG-HUVECs) and high-glucose human dermal fibroblasts <t>(HG-HDFs);</t> scale bar = 100 μm.
Primary Human Dermal Fibroblast Hdf Cells, supplied by Korean Cell Line Bank, 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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86
Fresenius Medical Care hv hdf
Isolation and characterization of chorionic plate mesenchymal stem cell (CP-MSC)-derived sEVs. (A) Schematic showing the isolation and characterization of sEVs derived from <t>CP-MSCs</t> <t>cultured</t> under O₂ Nor , O₂ Hypo-5% , or O₂ Hypo-3% conditions. (B) TEM images showing the typical bilayer structure of sEVs Nor , sEVs Hypo-5% , and sEVs Hypo-3% ; scale bar = 100 nm. (C) Nanoparticle tracking analysis (NTA) profiles showing the size distribution and concentration of sEVs Nor , sEVs Hypo-5% , and sEVs Hypo-3% after 400-fold dilution. (D) Western blotting analysis showing the expression of CD9, CD63, TSG101, and Calnexin proteins in these 3 sEVs. (E) Confocal microscopy images showing the internalization of Dil-labeled sEVs by high-glucose human umbilical vein endothelial cells (HG-HUVECs) and high-glucose human dermal fibroblasts <t>(HG-HDFs);</t> scale bar = 100 μm.
Hv Hdf, supplied by Fresenius Medical Care, 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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95
CLS Cell Lines Service GmbH human dermal fibroblasts hdfs
Assessment of resazurin reduction in <t>fibroblasts</t> <t>(HDFs)</t> for ( a ) hexane (bars in yellow) and ( b ) TBa (bars in red) extracts. Control cells (green bars) without the addition of test samples, for which viability was assumed to be 100%. Data are presented as mean ± SD ( n = 3). Statistical analysis was performed using one-way ANOVA followed by Dunnett’s multiple comparisons test. Differences were considered statistically significant at p < 0.05 (*), p < 0.01(**), p < 0.001(***), relative to the control.
Human Dermal Fibroblasts Hdfs, supplied by CLS Cell Lines Service GmbH, 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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Image Search Results


Isolation and characterization of chorionic plate mesenchymal stem cell (CP-MSC)-derived sEVs. (A) Schematic showing the isolation and characterization of sEVs derived from CP-MSCs cultured under O₂ Nor , O₂ Hypo-5% , or O₂ Hypo-3% conditions. (B) TEM images showing the typical bilayer structure of sEVs Nor , sEVs Hypo-5% , and sEVs Hypo-3% ; scale bar = 100 nm. (C) Nanoparticle tracking analysis (NTA) profiles showing the size distribution and concentration of sEVs Nor , sEVs Hypo-5% , and sEVs Hypo-3% after 400-fold dilution. (D) Western blotting analysis showing the expression of CD9, CD63, TSG101, and Calnexin proteins in these 3 sEVs. (E) Confocal microscopy images showing the internalization of Dil-labeled sEVs by high-glucose human umbilical vein endothelial cells (HG-HUVECs) and high-glucose human dermal fibroblasts (HG-HDFs); scale bar = 100 μm.

Journal: Research

Article Title: Hypoxia-Challenged sEVs-Engineered Nanofiber Scaffolds Accelerate Diabetic Wound Healing via Reversing Cellular Dysfunction of Skin Repair Cells

doi: 10.34133/research.1248

Figure Lengend Snippet: Isolation and characterization of chorionic plate mesenchymal stem cell (CP-MSC)-derived sEVs. (A) Schematic showing the isolation and characterization of sEVs derived from CP-MSCs cultured under O₂ Nor , O₂ Hypo-5% , or O₂ Hypo-3% conditions. (B) TEM images showing the typical bilayer structure of sEVs Nor , sEVs Hypo-5% , and sEVs Hypo-3% ; scale bar = 100 nm. (C) Nanoparticle tracking analysis (NTA) profiles showing the size distribution and concentration of sEVs Nor , sEVs Hypo-5% , and sEVs Hypo-3% after 400-fold dilution. (D) Western blotting analysis showing the expression of CD9, CD63, TSG101, and Calnexin proteins in these 3 sEVs. (E) Confocal microscopy images showing the internalization of Dil-labeled sEVs by high-glucose human umbilical vein endothelial cells (HG-HUVECs) and high-glucose human dermal fibroblasts (HG-HDFs); scale bar = 100 μm.

Article Snippet: HDFs (ATCC, CRL-4053, USA) were cultured in DMEM, containing 10% FBS, 1% PS, and 50 mM glucose for 60 d.

Techniques: Isolation, Derivative Assay, Cell Culture, Concentration Assay, Western Blot, Expressing, Confocal Microscopy, Labeling

Assessment of resazurin reduction in fibroblasts (HDFs) for ( a ) hexane (bars in yellow) and ( b ) TBa (bars in red) extracts. Control cells (green bars) without the addition of test samples, for which viability was assumed to be 100%. Data are presented as mean ± SD ( n = 3). Statistical analysis was performed using one-way ANOVA followed by Dunnett’s multiple comparisons test. Differences were considered statistically significant at p < 0.05 (*), p < 0.01(**), p < 0.001(***), relative to the control.

Journal: Molecules

Article Title: Volatile Natural Deep Eutectic Solvents (VNADESs) for Extraction of Shikonin Derivatives from Echium vulgare Roots and Evaluation of Biological Activity

doi: 10.3390/molecules31091434

Figure Lengend Snippet: Assessment of resazurin reduction in fibroblasts (HDFs) for ( a ) hexane (bars in yellow) and ( b ) TBa (bars in red) extracts. Control cells (green bars) without the addition of test samples, for which viability was assumed to be 100%. Data are presented as mean ± SD ( n = 3). Statistical analysis was performed using one-way ANOVA followed by Dunnett’s multiple comparisons test. Differences were considered statistically significant at p < 0.05 (*), p < 0.01(**), p < 0.001(***), relative to the control.

Article Snippet: Human dermal fibroblasts (HDFs) were obtained from CLS Cell Lines Service (Eppelheim, Germany) and were maintained in Dulbecco’s Modified Eagle’s Medium (DMEM; Biological Industries, Cromwell, CO, USA) supplemented with sodium pyruvate, L-glutamine, glucose (4.5 g/L), and 10% fetal bovine serum (FBS; Genos, Łódź, Poland).

Techniques: Control