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European Collection of Authenticated Cell Cultures human fetal foreskin fibroblasts
A549 and <t>HFFF2</t> cells viability 24 h after incubation with nanomaterials, measured by three different assays. Statistically significant difference between a group and the control is marked as * p < 0.05, ** p < 0.0021, *** p < 0.0002, p **** < 0.0001. MTT and NR results are presented as % of control (mean with standard variation). Blue bars, GO; red bars, Ag; purple, GO:Ag. Notes: MTT is based on mitochondrial succinate dehydrogenase activity; NR is based on lysosomal uptake of neutral red. LDH is based on leakage of cytosol lactic dehydrogenase
Human Fetal Foreskin Fibroblasts, supplied by European Collection of Authenticated Cell Cultures, 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/human+fetal+foreskin+fibroblasts/human+fetal+foreskin+fibroblasts/pmc11685253-90-0-7
Average 90 stars, based on 1 article reviews
human fetal foreskin fibroblasts - by Bioz Stars, 2026-09
90/100 stars

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1) Product Images from "The cytocompatibility of graphene oxide as a platform to enhance the effectiveness and safety of silver nanoparticles through in vitro studies"

Article Title: The cytocompatibility of graphene oxide as a platform to enhance the effectiveness and safety of silver nanoparticles through in vitro studies

Journal: Environmental Science and Pollution Research International

doi: 10.1007/s11356-023-30151-1

A549 and HFFF2 cells viability 24 h after incubation with nanomaterials, measured by three different assays. Statistically significant difference between a group and the control is marked as * p < 0.05, ** p < 0.0021, *** p < 0.0002, p **** < 0.0001. MTT and NR results are presented as % of control (mean with standard variation). Blue bars, GO; red bars, Ag; purple, GO:Ag. Notes: MTT is based on mitochondrial succinate dehydrogenase activity; NR is based on lysosomal uptake of neutral red. LDH is based on leakage of cytosol lactic dehydrogenase
Figure Legend Snippet: A549 and HFFF2 cells viability 24 h after incubation with nanomaterials, measured by three different assays. Statistically significant difference between a group and the control is marked as * p < 0.05, ** p < 0.0021, *** p < 0.0002, p **** < 0.0001. MTT and NR results are presented as % of control (mean with standard variation). Blue bars, GO; red bars, Ag; purple, GO:Ag. Notes: MTT is based on mitochondrial succinate dehydrogenase activity; NR is based on lysosomal uptake of neutral red. LDH is based on leakage of cytosol lactic dehydrogenase

Techniques Used: Incubation, Control, Activity Assay

A549 and HFFF2 cell proliferation rate after 24 h and 48 h of incubation with nanomaterials, measured by colorimetric BrdU assay. Statistically significant difference between a group and the control is marked as * p < 0.05, **** p < 0.0001. Results are presented as % of control (mean with standard variation). Blue bars, GO; red bars, Ag; purple, GO:Ag
Figure Legend Snippet: A549 and HFFF2 cell proliferation rate after 24 h and 48 h of incubation with nanomaterials, measured by colorimetric BrdU assay. Statistically significant difference between a group and the control is marked as * p < 0.05, **** p < 0.0001. Results are presented as % of control (mean with standard variation). Blue bars, GO; red bars, Ag; purple, GO:Ag

Techniques Used: Incubation, BrdU Staining, Control

Reactive oxygen species (ROS) level in A549 and HFFF2 cells after 2 h of incubation with nanomaterials, measured by colorimetric DCF-DA fluorometric assay. Statistically significant difference between a group and the control is marked as ** p < 0.0021, *** p < 0.0002, p **** < 0.0001. Results are presented as mean fluorescence intensity (MFI) with standard deviation. Blue bars, GO; red bars, Ag; purple, GO:Ag
Figure Legend Snippet: Reactive oxygen species (ROS) level in A549 and HFFF2 cells after 2 h of incubation with nanomaterials, measured by colorimetric DCF-DA fluorometric assay. Statistically significant difference between a group and the control is marked as ** p < 0.0021, *** p < 0.0002, p **** < 0.0001. Results are presented as mean fluorescence intensity (MFI) with standard deviation. Blue bars, GO; red bars, Ag; purple, GO:Ag

Techniques Used: Incubation, Control, Fluorescence, Standard Deviation

Caspase 3/7 activity in A549 and HFFF2 cells after 2 h of treatment with nanomaterials, measured by fluorometric CellEvent assay. There were no statistically significant differences. Results are presented as mean fluorescence intensity (MFI) with standard deviation. Blue bars, GO; red bars, Ag; purple, GO:Ag; green, additional controls
Figure Legend Snippet: Caspase 3/7 activity in A549 and HFFF2 cells after 2 h of treatment with nanomaterials, measured by fluorometric CellEvent assay. There were no statistically significant differences. Results are presented as mean fluorescence intensity (MFI) with standard deviation. Blue bars, GO; red bars, Ag; purple, GO:Ag; green, additional controls

Techniques Used: Activity Assay, Fluorescence, Standard Deviation

Confocal imaging of HFFF2 cells combined with caspase 3/7 activity detection after treatment with nanomaterials for 2 h. Additional positive control: ketoconazole. Scale bar 450 µm. Notes: Nuclei were stained with DAPI (blue), caspase- 3/7 activity was visualized using a CellEvent probe (green) which stains nuclei in the presence of active caspases; actin F was stained with phalloidin conjugated with Alexa Fluor 633 (red)
Figure Legend Snippet: Confocal imaging of HFFF2 cells combined with caspase 3/7 activity detection after treatment with nanomaterials for 2 h. Additional positive control: ketoconazole. Scale bar 450 µm. Notes: Nuclei were stained with DAPI (blue), caspase- 3/7 activity was visualized using a CellEvent probe (green) which stains nuclei in the presence of active caspases; actin F was stained with phalloidin conjugated with Alexa Fluor 633 (red)

Techniques Used: Imaging, Activity Assay, Positive Control, Staining

Selected magnified pictures from confocal imaging of A549 and HFFF2 cells combined with caspase- 3/7 activity detection after treatment with nanomaterials for 2 h. Additional positive controls: miconazole (A549) and ketoconazole (HFFF2). Scale bar 450 µm. Notes: Nuclei were stained with DAPI (blue); caspase 3/7 activity was visualized using a CellEvent probe (green, bright nuclei) which stains nuclei in the presence of active caspases; actin F was stained with phalloidin conjugated with Alexa Fluor 633 (red)
Figure Legend Snippet: Selected magnified pictures from confocal imaging of A549 and HFFF2 cells combined with caspase- 3/7 activity detection after treatment with nanomaterials for 2 h. Additional positive controls: miconazole (A549) and ketoconazole (HFFF2). Scale bar 450 µm. Notes: Nuclei were stained with DAPI (blue); caspase 3/7 activity was visualized using a CellEvent probe (green, bright nuclei) which stains nuclei in the presence of active caspases; actin F was stained with phalloidin conjugated with Alexa Fluor 633 (red)

Techniques Used: Imaging, Activity Assay, Staining

Live imaging of A549 (upper row) and HFFF2 (lower row) cells after 7 days of treatment with nanomaterials, which were introduced into the culture medium after cell adhesion
Figure Legend Snippet: Live imaging of A549 (upper row) and HFFF2 (lower row) cells after 7 days of treatment with nanomaterials, which were introduced into the culture medium after cell adhesion

Techniques Used: Imaging

Live imaging of HFFF2 cells after seeding on tissue culture plates coated with nanomaterials. Cells were grown for 24 h. Agglomerates of thicker GO flakes are visible. Scale bar 200 µm
Figure Legend Snippet: Live imaging of HFFF2 cells after seeding on tissue culture plates coated with nanomaterials. Cells were grown for 24 h. Agglomerates of thicker GO flakes are visible. Scale bar 200 µm

Techniques Used: Imaging

May–Grünwald and Giemsa staining of A549 (upper row) and HFFF2 (lower row) cells after 24 days after seeding on tissue culture plates coated with nanomaterials (selected images). Agglomerates of thicker GO flakes are visible in the A549 cell line; stained large and thin flakes are visible in the HFFF2 cell line. Scale bar 200 µm
Figure Legend Snippet: May–Grünwald and Giemsa staining of A549 (upper row) and HFFF2 (lower row) cells after 24 days after seeding on tissue culture plates coated with nanomaterials (selected images). Agglomerates of thicker GO flakes are visible in the A549 cell line; stained large and thin flakes are visible in the HFFF2 cell line. Scale bar 200 µm

Techniques Used: Staining

Related Articles

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Article Title: The cytocompatibility of graphene oxide as a platform to enhance the effectiveness and safety of silver nanoparticles through in vitro studies
Article Snippet: .. HFFF2, human fetal foreskin fibroblasts, from the European Collection of Authenticated Cell Cultures, catalogue no 86031405, is a cell line isolated from a 14 to 18 week old male fetus. ..



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European Collection of Authenticated Cell Cultures human fetal foreskin fibroblasts
A549 and <t>HFFF2</t> cells viability 24 h after incubation with nanomaterials, measured by three different assays. Statistically significant difference between a group and the control is marked as * p < 0.05, ** p < 0.0021, *** p < 0.0002, p **** < 0.0001. MTT and NR results are presented as % of control (mean with standard variation). Blue bars, GO; red bars, Ag; purple, GO:Ag. Notes: MTT is based on mitochondrial succinate dehydrogenase activity; NR is based on lysosomal uptake of neutral red. LDH is based on leakage of cytosol lactic dehydrogenase
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  Buy from Supplier

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A549 and HFFF2 cells viability 24 h after incubation with nanomaterials, measured by three different assays. Statistically significant difference between a group and the control is marked as * p < 0.05, ** p < 0.0021, *** p < 0.0002, p **** < 0.0001. MTT and NR results are presented as % of control (mean with standard variation). Blue bars, GO; red bars, Ag; purple, GO:Ag. Notes: MTT is based on mitochondrial succinate dehydrogenase activity; NR is based on lysosomal uptake of neutral red. LDH is based on leakage of cytosol lactic dehydrogenase

Journal: Environmental Science and Pollution Research International

Article Title: The cytocompatibility of graphene oxide as a platform to enhance the effectiveness and safety of silver nanoparticles through in vitro studies

doi: 10.1007/s11356-023-30151-1

Figure Lengend Snippet: A549 and HFFF2 cells viability 24 h after incubation with nanomaterials, measured by three different assays. Statistically significant difference between a group and the control is marked as * p < 0.05, ** p < 0.0021, *** p < 0.0002, p **** < 0.0001. MTT and NR results are presented as % of control (mean with standard variation). Blue bars, GO; red bars, Ag; purple, GO:Ag. Notes: MTT is based on mitochondrial succinate dehydrogenase activity; NR is based on lysosomal uptake of neutral red. LDH is based on leakage of cytosol lactic dehydrogenase

Article Snippet: HFFF2, human fetal foreskin fibroblasts, from the European Collection of Authenticated Cell Cultures, catalogue no 86031405, is a cell line isolated from a 14 to 18 week old male fetus.

Techniques: Incubation, Control, Activity Assay

A549 and HFFF2 cell proliferation rate after 24 h and 48 h of incubation with nanomaterials, measured by colorimetric BrdU assay. Statistically significant difference between a group and the control is marked as * p < 0.05, **** p < 0.0001. Results are presented as % of control (mean with standard variation). Blue bars, GO; red bars, Ag; purple, GO:Ag

Journal: Environmental Science and Pollution Research International

Article Title: The cytocompatibility of graphene oxide as a platform to enhance the effectiveness and safety of silver nanoparticles through in vitro studies

doi: 10.1007/s11356-023-30151-1

Figure Lengend Snippet: A549 and HFFF2 cell proliferation rate after 24 h and 48 h of incubation with nanomaterials, measured by colorimetric BrdU assay. Statistically significant difference between a group and the control is marked as * p < 0.05, **** p < 0.0001. Results are presented as % of control (mean with standard variation). Blue bars, GO; red bars, Ag; purple, GO:Ag

Article Snippet: HFFF2, human fetal foreskin fibroblasts, from the European Collection of Authenticated Cell Cultures, catalogue no 86031405, is a cell line isolated from a 14 to 18 week old male fetus.

Techniques: Incubation, BrdU Staining, Control

Reactive oxygen species (ROS) level in A549 and HFFF2 cells after 2 h of incubation with nanomaterials, measured by colorimetric DCF-DA fluorometric assay. Statistically significant difference between a group and the control is marked as ** p < 0.0021, *** p < 0.0002, p **** < 0.0001. Results are presented as mean fluorescence intensity (MFI) with standard deviation. Blue bars, GO; red bars, Ag; purple, GO:Ag

Journal: Environmental Science and Pollution Research International

Article Title: The cytocompatibility of graphene oxide as a platform to enhance the effectiveness and safety of silver nanoparticles through in vitro studies

doi: 10.1007/s11356-023-30151-1

Figure Lengend Snippet: Reactive oxygen species (ROS) level in A549 and HFFF2 cells after 2 h of incubation with nanomaterials, measured by colorimetric DCF-DA fluorometric assay. Statistically significant difference between a group and the control is marked as ** p < 0.0021, *** p < 0.0002, p **** < 0.0001. Results are presented as mean fluorescence intensity (MFI) with standard deviation. Blue bars, GO; red bars, Ag; purple, GO:Ag

Article Snippet: HFFF2, human fetal foreskin fibroblasts, from the European Collection of Authenticated Cell Cultures, catalogue no 86031405, is a cell line isolated from a 14 to 18 week old male fetus.

Techniques: Incubation, Control, Fluorescence, Standard Deviation

Caspase 3/7 activity in A549 and HFFF2 cells after 2 h of treatment with nanomaterials, measured by fluorometric CellEvent assay. There were no statistically significant differences. Results are presented as mean fluorescence intensity (MFI) with standard deviation. Blue bars, GO; red bars, Ag; purple, GO:Ag; green, additional controls

Journal: Environmental Science and Pollution Research International

Article Title: The cytocompatibility of graphene oxide as a platform to enhance the effectiveness and safety of silver nanoparticles through in vitro studies

doi: 10.1007/s11356-023-30151-1

Figure Lengend Snippet: Caspase 3/7 activity in A549 and HFFF2 cells after 2 h of treatment with nanomaterials, measured by fluorometric CellEvent assay. There were no statistically significant differences. Results are presented as mean fluorescence intensity (MFI) with standard deviation. Blue bars, GO; red bars, Ag; purple, GO:Ag; green, additional controls

Article Snippet: HFFF2, human fetal foreskin fibroblasts, from the European Collection of Authenticated Cell Cultures, catalogue no 86031405, is a cell line isolated from a 14 to 18 week old male fetus.

Techniques: Activity Assay, Fluorescence, Standard Deviation

Confocal imaging of HFFF2 cells combined with caspase 3/7 activity detection after treatment with nanomaterials for 2 h. Additional positive control: ketoconazole. Scale bar 450 µm. Notes: Nuclei were stained with DAPI (blue), caspase- 3/7 activity was visualized using a CellEvent probe (green) which stains nuclei in the presence of active caspases; actin F was stained with phalloidin conjugated with Alexa Fluor 633 (red)

Journal: Environmental Science and Pollution Research International

Article Title: The cytocompatibility of graphene oxide as a platform to enhance the effectiveness and safety of silver nanoparticles through in vitro studies

doi: 10.1007/s11356-023-30151-1

Figure Lengend Snippet: Confocal imaging of HFFF2 cells combined with caspase 3/7 activity detection after treatment with nanomaterials for 2 h. Additional positive control: ketoconazole. Scale bar 450 µm. Notes: Nuclei were stained with DAPI (blue), caspase- 3/7 activity was visualized using a CellEvent probe (green) which stains nuclei in the presence of active caspases; actin F was stained with phalloidin conjugated with Alexa Fluor 633 (red)

Article Snippet: HFFF2, human fetal foreskin fibroblasts, from the European Collection of Authenticated Cell Cultures, catalogue no 86031405, is a cell line isolated from a 14 to 18 week old male fetus.

Techniques: Imaging, Activity Assay, Positive Control, Staining

Selected magnified pictures from confocal imaging of A549 and HFFF2 cells combined with caspase- 3/7 activity detection after treatment with nanomaterials for 2 h. Additional positive controls: miconazole (A549) and ketoconazole (HFFF2). Scale bar 450 µm. Notes: Nuclei were stained with DAPI (blue); caspase 3/7 activity was visualized using a CellEvent probe (green, bright nuclei) which stains nuclei in the presence of active caspases; actin F was stained with phalloidin conjugated with Alexa Fluor 633 (red)

Journal: Environmental Science and Pollution Research International

Article Title: The cytocompatibility of graphene oxide as a platform to enhance the effectiveness and safety of silver nanoparticles through in vitro studies

doi: 10.1007/s11356-023-30151-1

Figure Lengend Snippet: Selected magnified pictures from confocal imaging of A549 and HFFF2 cells combined with caspase- 3/7 activity detection after treatment with nanomaterials for 2 h. Additional positive controls: miconazole (A549) and ketoconazole (HFFF2). Scale bar 450 µm. Notes: Nuclei were stained with DAPI (blue); caspase 3/7 activity was visualized using a CellEvent probe (green, bright nuclei) which stains nuclei in the presence of active caspases; actin F was stained with phalloidin conjugated with Alexa Fluor 633 (red)

Article Snippet: HFFF2, human fetal foreskin fibroblasts, from the European Collection of Authenticated Cell Cultures, catalogue no 86031405, is a cell line isolated from a 14 to 18 week old male fetus.

Techniques: Imaging, Activity Assay, Staining

Live imaging of A549 (upper row) and HFFF2 (lower row) cells after 7 days of treatment with nanomaterials, which were introduced into the culture medium after cell adhesion

Journal: Environmental Science and Pollution Research International

Article Title: The cytocompatibility of graphene oxide as a platform to enhance the effectiveness and safety of silver nanoparticles through in vitro studies

doi: 10.1007/s11356-023-30151-1

Figure Lengend Snippet: Live imaging of A549 (upper row) and HFFF2 (lower row) cells after 7 days of treatment with nanomaterials, which were introduced into the culture medium after cell adhesion

Article Snippet: HFFF2, human fetal foreskin fibroblasts, from the European Collection of Authenticated Cell Cultures, catalogue no 86031405, is a cell line isolated from a 14 to 18 week old male fetus.

Techniques: Imaging

Live imaging of HFFF2 cells after seeding on tissue culture plates coated with nanomaterials. Cells were grown for 24 h. Agglomerates of thicker GO flakes are visible. Scale bar 200 µm

Journal: Environmental Science and Pollution Research International

Article Title: The cytocompatibility of graphene oxide as a platform to enhance the effectiveness and safety of silver nanoparticles through in vitro studies

doi: 10.1007/s11356-023-30151-1

Figure Lengend Snippet: Live imaging of HFFF2 cells after seeding on tissue culture plates coated with nanomaterials. Cells were grown for 24 h. Agglomerates of thicker GO flakes are visible. Scale bar 200 µm

Article Snippet: HFFF2, human fetal foreskin fibroblasts, from the European Collection of Authenticated Cell Cultures, catalogue no 86031405, is a cell line isolated from a 14 to 18 week old male fetus.

Techniques: Imaging

May–Grünwald and Giemsa staining of A549 (upper row) and HFFF2 (lower row) cells after 24 days after seeding on tissue culture plates coated with nanomaterials (selected images). Agglomerates of thicker GO flakes are visible in the A549 cell line; stained large and thin flakes are visible in the HFFF2 cell line. Scale bar 200 µm

Journal: Environmental Science and Pollution Research International

Article Title: The cytocompatibility of graphene oxide as a platform to enhance the effectiveness and safety of silver nanoparticles through in vitro studies

doi: 10.1007/s11356-023-30151-1

Figure Lengend Snippet: May–Grünwald and Giemsa staining of A549 (upper row) and HFFF2 (lower row) cells after 24 days after seeding on tissue culture plates coated with nanomaterials (selected images). Agglomerates of thicker GO flakes are visible in the A549 cell line; stained large and thin flakes are visible in the HFFF2 cell line. Scale bar 200 µm

Article Snippet: HFFF2, human fetal foreskin fibroblasts, from the European Collection of Authenticated Cell Cultures, catalogue no 86031405, is a cell line isolated from a 14 to 18 week old male fetus.

Techniques: Staining