human foreskin fibroblasts hffs  (ATCC)


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    ATCC human foreskin fibroblasts hffs
    Human Foreskin Fibroblasts Hffs, supplied by ATCC, 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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    human foreskin fibroblast hff cells  (ATCC)


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    ATCC human foreskin fibroblast hff cells
    Human Foreskin Fibroblast Hff Cells, supplied by ATCC, 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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    healthy hff 1 line human fibroblasts  (ATCC)


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    ATCC healthy hff 1 line human fibroblasts
    Viability of healthy human cells <t>(HFF-1)</t> exposed to nanoliposome-encapsulated tarin (upper panels) and free tarin (bottom panels) for 24 h and 48 h. The viability of HFF-1 cells in cultures was determined employing resazurin as an indicator. The x-axis in the upper panel refers to the encapsulated tarin concentration, while empty liposomes refer to the corresponding volume of liposomal solution used to reach that concentration. *p< 0.05 compared to the control. ns – non-significant relative to the control.
    Healthy Hff 1 Line Human Fibroblasts, supplied by ATCC, 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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    1) Product Images from "Tarin-Loaded Nanoliposomes Activate Apoptosis and Autophagy and Inhibit the Migration of Human Mammary Adenocarcinoma Cells"

    Article Title: Tarin-Loaded Nanoliposomes Activate Apoptosis and Autophagy and Inhibit the Migration of Human Mammary Adenocarcinoma Cells

    Journal: International Journal of Nanomedicine

    doi: 10.2147/IJN.S434626

    Viability of healthy human cells (HFF-1) exposed to nanoliposome-encapsulated tarin (upper panels) and free tarin (bottom panels) for 24 h and 48 h. The viability of HFF-1 cells in cultures was determined employing resazurin as an indicator. The x-axis in the upper panel refers to the encapsulated tarin concentration, while empty liposomes refer to the corresponding volume of liposomal solution used to reach that concentration. *p< 0.05 compared to the control. ns – non-significant relative to the control.
    Figure Legend Snippet: Viability of healthy human cells (HFF-1) exposed to nanoliposome-encapsulated tarin (upper panels) and free tarin (bottom panels) for 24 h and 48 h. The viability of HFF-1 cells in cultures was determined employing resazurin as an indicator. The x-axis in the upper panel refers to the encapsulated tarin concentration, while empty liposomes refer to the corresponding volume of liposomal solution used to reach that concentration. *p< 0.05 compared to the control. ns – non-significant relative to the control.

    Techniques Used: Concentration Assay, Liposomes

    human foreskin fibroblasts hffs  (ATCC)


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    ATCC human foreskin fibroblasts hffs

    Human Foreskin Fibroblasts Hffs, supplied by ATCC, 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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    1) Product Images from "Analysis of CDPK1 targets identifies a trafficking adaptor complex that regulates microneme exocytosis in Toxoplasma"

    Article Title: Analysis of CDPK1 targets identifies a trafficking adaptor complex that regulates microneme exocytosis in Toxoplasma

    Journal: eLife

    doi: 10.7554/eLife.85654


    Figure Legend Snippet:

    Techniques Used: Recombinant, Sequencing, Modification, Sample Prep, Peptide Fractionation, Magnetic Beads, Software, Mass Spectrometry, Cell Culture, Protease Inhibitor, Immunoprecipitation, Lysis

    human foreskin fibroblasts hff 1 cell line  (ATCC)


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    ATCC human foreskin fibroblasts hff 1 cell line
    Cell viability ( a ) and cytotoxicity ( b ) of TOH-treated human foreskin fibroblasts (HFF- 1) cells at 37 °C as determined by MTT, Mitogreen, LDH, and dual AO/EB staining assays. Percentages of cell viability and cytotoxicity were shown as mean ± SD. *P < 0.05 and ****P < 0.0001 indicate significant differences compared with the control group (concentration 0). TOH Tryptophol, VOZ voriconazole.
    Human Foreskin Fibroblasts Hff 1 Cell Line, supplied by ATCC, 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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    1) Product Images from "The study of tryptophol containing emulgel on fungal reduction and skin irritation"

    Article Title: The study of tryptophol containing emulgel on fungal reduction and skin irritation

    Journal: Scientific Reports

    doi: 10.1038/s41598-023-46121-z

    Cell viability ( a ) and cytotoxicity ( b ) of TOH-treated human foreskin fibroblasts (HFF- 1) cells at 37 °C as determined by MTT, Mitogreen, LDH, and dual AO/EB staining assays. Percentages of cell viability and cytotoxicity were shown as mean ± SD. *P < 0.05 and ****P < 0.0001 indicate significant differences compared with the control group (concentration 0). TOH Tryptophol, VOZ voriconazole.
    Figure Legend Snippet: Cell viability ( a ) and cytotoxicity ( b ) of TOH-treated human foreskin fibroblasts (HFF- 1) cells at 37 °C as determined by MTT, Mitogreen, LDH, and dual AO/EB staining assays. Percentages of cell viability and cytotoxicity were shown as mean ± SD. *P < 0.05 and ****P < 0.0001 indicate significant differences compared with the control group (concentration 0). TOH Tryptophol, VOZ voriconazole.

    Techniques Used: Staining, Concentration Assay

    human foreskin fibroblasts hff  (ATCC)


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    ATCC human foreskin fibroblasts hff
    Effect of known anti-toxoplasma agents (A) and pyrimidine analogues (B) on <t>intracellular</t> <t>tachyzoites</t> and on uninfected <t>HFF</t> cells (C). Data were plotted to a log[Inhibitor] vs response sigmoid model with variable slope (A, B) or an equation for two-site competition (C) in Prims 9 to determine EC 50 values. The curves are single experiments, representative of at least 2 (pyrimethamine) or 3 (all other compounds) independent, identically-performed experiments.
    Human Foreskin Fibroblasts Hff, supplied by ATCC, 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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    1) Product Images from "Pyrimidine salvage in Toxoplasma gondii as a target for new treatment"

    Article Title: Pyrimidine salvage in Toxoplasma gondii as a target for new treatment

    Journal: bioRxiv

    doi: 10.1101/2023.11.01.565095

    Effect of known anti-toxoplasma agents (A) and pyrimidine analogues (B) on intracellular tachyzoites and on uninfected HFF cells (C). Data were plotted to a log[Inhibitor] vs response sigmoid model with variable slope (A, B) or an equation for two-site competition (C) in Prims 9 to determine EC 50 values. The curves are single experiments, representative of at least 2 (pyrimethamine) or 3 (all other compounds) independent, identically-performed experiments.
    Figure Legend Snippet: Effect of known anti-toxoplasma agents (A) and pyrimidine analogues (B) on intracellular tachyzoites and on uninfected HFF cells (C). Data were plotted to a log[Inhibitor] vs response sigmoid model with variable slope (A, B) or an equation for two-site competition (C) in Prims 9 to determine EC 50 values. The curves are single experiments, representative of at least 2 (pyrimethamine) or 3 (all other compounds) independent, identically-performed experiments.

    Techniques Used: Analogues


    Figure Legend Snippet:

    Techniques Used: In Vitro

    human fibroblast cells human foreskin fibroblast hff cells  (ATCC)


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    ATCC human fibroblast cells human foreskin fibroblast hff cells
    Human Fibroblast Cells Human Foreskin Fibroblast Hff Cells, supplied by ATCC, 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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    human foreskin fibroblast cell line hff  (ATCC)


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    ATCC human foreskin fibroblast cell line hff
    Effects of varying DNX concentrations on the cytotoxicity of human foreskin fibroblast cells <t>(HFF-1)</t> observed at ( A ) 24 h and ( B ) 48 h. Values are represented as mean ± standard error of mean. * p < 0.05 vs. 0 µM DNX groups.
    Human Foreskin Fibroblast Cell Line Hff, supplied by ATCC, 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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    1) Product Images from "Extremophilic Solutions: The Role of Deinoxanthin in Counteracting UV-Induced Skin Harm"

    Article Title: Extremophilic Solutions: The Role of Deinoxanthin in Counteracting UV-Induced Skin Harm

    Journal: Current Issues in Molecular Biology

    doi: 10.3390/cimb45100528

    Effects of varying DNX concentrations on the cytotoxicity of human foreskin fibroblast cells (HFF-1) observed at ( A ) 24 h and ( B ) 48 h. Values are represented as mean ± standard error of mean. * p < 0.05 vs. 0 µM DNX groups.
    Figure Legend Snippet: Effects of varying DNX concentrations on the cytotoxicity of human foreskin fibroblast cells (HFF-1) observed at ( A ) 24 h and ( B ) 48 h. Values are represented as mean ± standard error of mean. * p < 0.05 vs. 0 µM DNX groups.

    Techniques Used:

    Protective effects of varying concentrations of DNX on HFF-1 cells exposed to UVB and UVA radiation observed at ( A ) UVA and ( B ) UVB. Statistical significance in this figure indicates the observed differences between the control group and the groups treated with varying concentrations of DNX and VitC, all subjected to the same UV dosage levels. The results are presented as the mean ± s.e.m. ( n = 6). * p < 0.05; ** p < 0.001; *** p < 0.005.
    Figure Legend Snippet: Protective effects of varying concentrations of DNX on HFF-1 cells exposed to UVB and UVA radiation observed at ( A ) UVA and ( B ) UVB. Statistical significance in this figure indicates the observed differences between the control group and the groups treated with varying concentrations of DNX and VitC, all subjected to the same UV dosage levels. The results are presented as the mean ± s.e.m. ( n = 6). * p < 0.05; ** p < 0.001; *** p < 0.005.

    Techniques Used:

    Evaluation of apoptosis-associated parameters in HFF-1 cells: viable and apoptotic cells were quantified. Each group used three wells for Annexin V-FITC/PI staining. Population analyses were performed in triplicate, and the entire assay was repeated three times.
    Figure Legend Snippet: Evaluation of apoptosis-associated parameters in HFF-1 cells: viable and apoptotic cells were quantified. Each group used three wells for Annexin V-FITC/PI staining. Population analyses were performed in triplicate, and the entire assay was repeated three times.

    Techniques Used: Staining

    Activity of tyrosinase in HFF-1 cells exposed to UVA ( A ) and UVB ( B ) radiation was determined after treatment with varying concentrations of DNX. Statistical significance in this figure indicates the observed differences between the control group and the groups treated with varying concentrations of DNX and VitC, all subjected to the same UV dosage levels. The mean percentages ± s.e.m. are shown ( n = 6). * p < 0.05; ** p < 0.001; *** p < 0.005.
    Figure Legend Snippet: Activity of tyrosinase in HFF-1 cells exposed to UVA ( A ) and UVB ( B ) radiation was determined after treatment with varying concentrations of DNX. Statistical significance in this figure indicates the observed differences between the control group and the groups treated with varying concentrations of DNX and VitC, all subjected to the same UV dosage levels. The mean percentages ± s.e.m. are shown ( n = 6). * p < 0.05; ** p < 0.001; *** p < 0.005.

    Techniques Used: Activity Assay

    Activity of SOD in HFF-1 cell after UVA and UVB irradiation with different concentrations of DNX and VitC. Values are represented as mean ± standard error of mean. a p < 0.05 vs. control group. b p < 0.05 vs. UVA group. c p < 0.05 VitC-treated + UVA group. d p < 0.05 UVB group. e p < 0.05 VitC-treated + UVB group.
    Figure Legend Snippet: Activity of SOD in HFF-1 cell after UVA and UVB irradiation with different concentrations of DNX and VitC. Values are represented as mean ± standard error of mean. a p < 0.05 vs. control group. b p < 0.05 vs. UVA group. c p < 0.05 VitC-treated + UVA group. d p < 0.05 UVB group. e p < 0.05 VitC-treated + UVB group.

    Techniques Used: Activity Assay, Irradiation

    ( A ) ROS level in HFF-1 cells post UVA and UVB exposure, influenced by varying concentrations of DNX ( B ) MDA in HFF-1 cell after UVA and UVB irradiation with varying concentrations of DNX. Values are represented as mean ± standard error of mean. a p < 0.05 vs. control group. b p < 0.05 vs. UVA group. c p < 0.05 VitC-treated + UVA group. d p < 0.05 UVB group. e p < 0.05 VitC-treated + UVB group.
    Figure Legend Snippet: ( A ) ROS level in HFF-1 cells post UVA and UVB exposure, influenced by varying concentrations of DNX ( B ) MDA in HFF-1 cell after UVA and UVB irradiation with varying concentrations of DNX. Values are represented as mean ± standard error of mean. a p < 0.05 vs. control group. b p < 0.05 vs. UVA group. c p < 0.05 VitC-treated + UVA group. d p < 0.05 UVB group. e p < 0.05 VitC-treated + UVB group.

    Techniques Used: Irradiation

    Hydroxyproline formation in HFF-1 cell after UVA and UVB irradiation with varying concentrations of DNX and VitC. Values are represented as mean ± standard error of mean. a p < 0.05 vs. control group. b p < 0.05 vs. UVA group. c p < 0.05 VitC-treated + UVA group. d p < 0.05 UVB group. e p < 0.05 VitC-treated + UVB group.
    Figure Legend Snippet: Hydroxyproline formation in HFF-1 cell after UVA and UVB irradiation with varying concentrations of DNX and VitC. Values are represented as mean ± standard error of mean. a p < 0.05 vs. control group. b p < 0.05 vs. UVA group. c p < 0.05 VitC-treated + UVA group. d p < 0.05 UVB group. e p < 0.05 VitC-treated + UVB group.

    Techniques Used: Irradiation

    Impact of DNX on the wound healing response in UVA-exposed HFF-1 cells. ( A ) DNX counteracts the impediments in wound healing caused by UVA exposure. Upon reaching confluency, cells were scratched using a pipette tip and subsequently pretreated with DNX and VitC before UVA exposure. Inverted images (40× magnifications, 400 µm scale bar) of the scratched HFF-1 cells were captured at the 0 and 24 h marks post irradiation. ( B ) The wound healing assay’s graph, representing % wound closure, was generated by analyzing the captured inverted images through the Image-Pro Plus 6.0 Software. Data are expressed as the mean ± standard deviation of three independent experiments. Ns: non-significance, * p < 0.05.
    Figure Legend Snippet: Impact of DNX on the wound healing response in UVA-exposed HFF-1 cells. ( A ) DNX counteracts the impediments in wound healing caused by UVA exposure. Upon reaching confluency, cells were scratched using a pipette tip and subsequently pretreated with DNX and VitC before UVA exposure. Inverted images (40× magnifications, 400 µm scale bar) of the scratched HFF-1 cells were captured at the 0 and 24 h marks post irradiation. ( B ) The wound healing assay’s graph, representing % wound closure, was generated by analyzing the captured inverted images through the Image-Pro Plus 6.0 Software. Data are expressed as the mean ± standard deviation of three independent experiments. Ns: non-significance, * p < 0.05.

    Techniques Used: Transferring, Irradiation, Generated, Software, Standard Deviation

    Effect of DNX on scratch wound healing in UVB-irradiated HFF-1 cells. ( A ) DNX rescues the UVB-induced wound-healing defect. Confluent cells were mechanically scratched with a pipette tip and pretreated with DNX and VitC prior to UVB irradiation. Invert micrographs (40× magnifications, 400 µm scale bar) of scratched HFF-1 cells were taken at 0 and 24 h following irradiation. ( B ) In the wound healing assay, the graph of % wound closure was derived from the assessment of inverted micrographs using Image-Pro Plus 6.0 Software. Data are expressed as the mean ± standard deviation of three independent experiments. ns: non-significance, * p < 0.05.
    Figure Legend Snippet: Effect of DNX on scratch wound healing in UVB-irradiated HFF-1 cells. ( A ) DNX rescues the UVB-induced wound-healing defect. Confluent cells were mechanically scratched with a pipette tip and pretreated with DNX and VitC prior to UVB irradiation. Invert micrographs (40× magnifications, 400 µm scale bar) of scratched HFF-1 cells were taken at 0 and 24 h following irradiation. ( B ) In the wound healing assay, the graph of % wound closure was derived from the assessment of inverted micrographs using Image-Pro Plus 6.0 Software. Data are expressed as the mean ± standard deviation of three independent experiments. ns: non-significance, * p < 0.05.

    Techniques Used: Irradiation, Transferring, Wound Healing Assay, Derivative Assay, Software, Standard Deviation

    primary human foreskin fibroblasts hffs  (ATCC)


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    ATCC primary human foreskin fibroblasts hffs
    Primary Human Foreskin Fibroblasts Hffs, supplied by ATCC, 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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    viruses primary human foreskin fibroblasts hffs  (ATCC)


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    ATCC viruses primary human foreskin fibroblasts hffs
    Viruses Primary Human Foreskin Fibroblasts Hffs, supplied by ATCC, 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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    ATCC human foreskin fibroblasts hffs
    Human Foreskin Fibroblasts Hffs, supplied by ATCC, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/human foreskin fibroblasts hffs/product/ATCC
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    ATCC human foreskin fibroblast hff cells
    Human Foreskin Fibroblast Hff Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/human foreskin fibroblast hff cells/product/ATCC
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    ATCC healthy hff 1 line human fibroblasts
    Viability of healthy human cells <t>(HFF-1)</t> exposed to nanoliposome-encapsulated tarin (upper panels) and free tarin (bottom panels) for 24 h and 48 h. The viability of HFF-1 cells in cultures was determined employing resazurin as an indicator. The x-axis in the upper panel refers to the encapsulated tarin concentration, while empty liposomes refer to the corresponding volume of liposomal solution used to reach that concentration. *p< 0.05 compared to the control. ns – non-significant relative to the control.
    Healthy Hff 1 Line Human Fibroblasts, supplied by ATCC, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/healthy hff 1 line human fibroblasts/product/ATCC
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    ATCC human foreskin fibroblasts hff 1 cell line
    Cell viability ( a ) and cytotoxicity ( b ) of TOH-treated human foreskin fibroblasts (HFF- 1) cells at 37 °C as determined by MTT, Mitogreen, LDH, and dual AO/EB staining assays. Percentages of cell viability and cytotoxicity were shown as mean ± SD. *P < 0.05 and ****P < 0.0001 indicate significant differences compared with the control group (concentration 0). TOH Tryptophol, VOZ voriconazole.
    Human Foreskin Fibroblasts Hff 1 Cell Line, supplied by ATCC, 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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    ATCC human foreskin fibroblasts hff
    Effect of known anti-toxoplasma agents (A) and pyrimidine analogues (B) on <t>intracellular</t> <t>tachyzoites</t> and on uninfected <t>HFF</t> cells (C). Data were plotted to a log[Inhibitor] vs response sigmoid model with variable slope (A, B) or an equation for two-site competition (C) in Prims 9 to determine EC 50 values. The curves are single experiments, representative of at least 2 (pyrimethamine) or 3 (all other compounds) independent, identically-performed experiments.
    Human Foreskin Fibroblasts Hff, supplied by ATCC, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/human foreskin fibroblasts hff/product/ATCC
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    ATCC human fibroblast cells human foreskin fibroblast hff cells
    Effect of known anti-toxoplasma agents (A) and pyrimidine analogues (B) on <t>intracellular</t> <t>tachyzoites</t> and on uninfected <t>HFF</t> cells (C). Data were plotted to a log[Inhibitor] vs response sigmoid model with variable slope (A, B) or an equation for two-site competition (C) in Prims 9 to determine EC 50 values. The curves are single experiments, representative of at least 2 (pyrimethamine) or 3 (all other compounds) independent, identically-performed experiments.
    Human Fibroblast Cells Human Foreskin Fibroblast Hff Cells, supplied by ATCC, 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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    ATCC human foreskin fibroblast cell line hff
    Effects of varying DNX concentrations on the cytotoxicity of human foreskin fibroblast cells <t>(HFF-1)</t> observed at ( A ) 24 h and ( B ) 48 h. Values are represented as mean ± standard error of mean. * p < 0.05 vs. 0 µM DNX groups.
    Human Foreskin Fibroblast Cell Line Hff, supplied by ATCC, 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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    ATCC primary human foreskin fibroblasts hffs
    Effects of varying DNX concentrations on the cytotoxicity of human foreskin fibroblast cells <t>(HFF-1)</t> observed at ( A ) 24 h and ( B ) 48 h. Values are represented as mean ± standard error of mean. * p < 0.05 vs. 0 µM DNX groups.
    Primary Human Foreskin Fibroblasts Hffs, supplied by ATCC, 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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    Average 86 stars, based on 1 article reviews
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    primary human foreskin fibroblasts hffs - by Bioz Stars, 2023-11
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    86
    ATCC viruses primary human foreskin fibroblasts hffs
    Effects of varying DNX concentrations on the cytotoxicity of human foreskin fibroblast cells <t>(HFF-1)</t> observed at ( A ) 24 h and ( B ) 48 h. Values are represented as mean ± standard error of mean. * p < 0.05 vs. 0 µM DNX groups.
    Viruses Primary Human Foreskin Fibroblasts Hffs, supplied by ATCC, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/viruses primary human foreskin fibroblasts hffs/product/ATCC
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    viruses primary human foreskin fibroblasts hffs - by Bioz Stars, 2023-11
    86/100 stars
      Buy from Supplier

    Image Search Results


    Viability of healthy human cells (HFF-1) exposed to nanoliposome-encapsulated tarin (upper panels) and free tarin (bottom panels) for 24 h and 48 h. The viability of HFF-1 cells in cultures was determined employing resazurin as an indicator. The x-axis in the upper panel refers to the encapsulated tarin concentration, while empty liposomes refer to the corresponding volume of liposomal solution used to reach that concentration. *p< 0.05 compared to the control. ns – non-significant relative to the control.

    Journal: International Journal of Nanomedicine

    Article Title: Tarin-Loaded Nanoliposomes Activate Apoptosis and Autophagy and Inhibit the Migration of Human Mammary Adenocarcinoma Cells

    doi: 10.2147/IJN.S434626

    Figure Lengend Snippet: Viability of healthy human cells (HFF-1) exposed to nanoliposome-encapsulated tarin (upper panels) and free tarin (bottom panels) for 24 h and 48 h. The viability of HFF-1 cells in cultures was determined employing resazurin as an indicator. The x-axis in the upper panel refers to the encapsulated tarin concentration, while empty liposomes refer to the corresponding volume of liposomal solution used to reach that concentration. *p< 0.05 compared to the control. ns – non-significant relative to the control.

    Article Snippet: Healthy HFF-1 line human fibroblasts (ATCC SCRC-1041) and MDA-MB-231 line human mammary adenocarcinoma cells (ATCC HTB-26) were obtained from the Rio de Janeiro Cell Bank (BCRJ), RJ, BRA available at https://bcrj.org.br/ .

    Techniques: Concentration Assay, Liposomes

    Cell viability ( a ) and cytotoxicity ( b ) of TOH-treated human foreskin fibroblasts (HFF- 1) cells at 37 °C as determined by MTT, Mitogreen, LDH, and dual AO/EB staining assays. Percentages of cell viability and cytotoxicity were shown as mean ± SD. *P < 0.05 and ****P < 0.0001 indicate significant differences compared with the control group (concentration 0). TOH Tryptophol, VOZ voriconazole.

    Journal: Scientific Reports

    Article Title: The study of tryptophol containing emulgel on fungal reduction and skin irritation

    doi: 10.1038/s41598-023-46121-z

    Figure Lengend Snippet: Cell viability ( a ) and cytotoxicity ( b ) of TOH-treated human foreskin fibroblasts (HFF- 1) cells at 37 °C as determined by MTT, Mitogreen, LDH, and dual AO/EB staining assays. Percentages of cell viability and cytotoxicity were shown as mean ± SD. *P < 0.05 and ****P < 0.0001 indicate significant differences compared with the control group (concentration 0). TOH Tryptophol, VOZ voriconazole.

    Article Snippet: Human foreskin fibroblasts (HFF-1) cell line (ATCC #SCRC-1041™) was used to investigate cell viability and cytotoxicity after TOH treatments.

    Techniques: Staining, Concentration Assay

    Effect of known anti-toxoplasma agents (A) and pyrimidine analogues (B) on intracellular tachyzoites and on uninfected HFF cells (C). Data were plotted to a log[Inhibitor] vs response sigmoid model with variable slope (A, B) or an equation for two-site competition (C) in Prims 9 to determine EC 50 values. The curves are single experiments, representative of at least 2 (pyrimethamine) or 3 (all other compounds) independent, identically-performed experiments.

    Journal: bioRxiv

    Article Title: Pyrimidine salvage in Toxoplasma gondii as a target for new treatment

    doi: 10.1101/2023.11.01.565095

    Figure Lengend Snippet: Effect of known anti-toxoplasma agents (A) and pyrimidine analogues (B) on intracellular tachyzoites and on uninfected HFF cells (C). Data were plotted to a log[Inhibitor] vs response sigmoid model with variable slope (A, B) or an equation for two-site competition (C) in Prims 9 to determine EC 50 values. The curves are single experiments, representative of at least 2 (pyrimethamine) or 3 (all other compounds) independent, identically-performed experiments.

    Article Snippet: T. gondii tachyzoites were cultured in human foreskin fibroblasts (HFF), sourced from ATCC (SCRC-1041).

    Techniques: Analogues

    Journal: bioRxiv

    Article Title: Pyrimidine salvage in Toxoplasma gondii as a target for new treatment

    doi: 10.1101/2023.11.01.565095

    Figure Lengend Snippet:

    Article Snippet: T. gondii tachyzoites were cultured in human foreskin fibroblasts (HFF), sourced from ATCC (SCRC-1041).

    Techniques: In Vitro

    Effects of varying DNX concentrations on the cytotoxicity of human foreskin fibroblast cells (HFF-1) observed at ( A ) 24 h and ( B ) 48 h. Values are represented as mean ± standard error of mean. * p < 0.05 vs. 0 µM DNX groups.

    Journal: Current Issues in Molecular Biology

    Article Title: Extremophilic Solutions: The Role of Deinoxanthin in Counteracting UV-Induced Skin Harm

    doi: 10.3390/cimb45100528

    Figure Lengend Snippet: Effects of varying DNX concentrations on the cytotoxicity of human foreskin fibroblast cells (HFF-1) observed at ( A ) 24 h and ( B ) 48 h. Values are represented as mean ± standard error of mean. * p < 0.05 vs. 0 µM DNX groups.

    Article Snippet: The human foreskin fibroblast cell line HFF-1 was obtained from ATCC (American Type Culture Collection, Manassas, VA, USA, LGC Promochem, Teddington, UK).

    Techniques:

    Protective effects of varying concentrations of DNX on HFF-1 cells exposed to UVB and UVA radiation observed at ( A ) UVA and ( B ) UVB. Statistical significance in this figure indicates the observed differences between the control group and the groups treated with varying concentrations of DNX and VitC, all subjected to the same UV dosage levels. The results are presented as the mean ± s.e.m. ( n = 6). * p < 0.05; ** p < 0.001; *** p < 0.005.

    Journal: Current Issues in Molecular Biology

    Article Title: Extremophilic Solutions: The Role of Deinoxanthin in Counteracting UV-Induced Skin Harm

    doi: 10.3390/cimb45100528

    Figure Lengend Snippet: Protective effects of varying concentrations of DNX on HFF-1 cells exposed to UVB and UVA radiation observed at ( A ) UVA and ( B ) UVB. Statistical significance in this figure indicates the observed differences between the control group and the groups treated with varying concentrations of DNX and VitC, all subjected to the same UV dosage levels. The results are presented as the mean ± s.e.m. ( n = 6). * p < 0.05; ** p < 0.001; *** p < 0.005.

    Article Snippet: The human foreskin fibroblast cell line HFF-1 was obtained from ATCC (American Type Culture Collection, Manassas, VA, USA, LGC Promochem, Teddington, UK).

    Techniques:

    Evaluation of apoptosis-associated parameters in HFF-1 cells: viable and apoptotic cells were quantified. Each group used three wells for Annexin V-FITC/PI staining. Population analyses were performed in triplicate, and the entire assay was repeated three times.

    Journal: Current Issues in Molecular Biology

    Article Title: Extremophilic Solutions: The Role of Deinoxanthin in Counteracting UV-Induced Skin Harm

    doi: 10.3390/cimb45100528

    Figure Lengend Snippet: Evaluation of apoptosis-associated parameters in HFF-1 cells: viable and apoptotic cells were quantified. Each group used three wells for Annexin V-FITC/PI staining. Population analyses were performed in triplicate, and the entire assay was repeated three times.

    Article Snippet: The human foreskin fibroblast cell line HFF-1 was obtained from ATCC (American Type Culture Collection, Manassas, VA, USA, LGC Promochem, Teddington, UK).

    Techniques: Staining

    Activity of tyrosinase in HFF-1 cells exposed to UVA ( A ) and UVB ( B ) radiation was determined after treatment with varying concentrations of DNX. Statistical significance in this figure indicates the observed differences between the control group and the groups treated with varying concentrations of DNX and VitC, all subjected to the same UV dosage levels. The mean percentages ± s.e.m. are shown ( n = 6). * p < 0.05; ** p < 0.001; *** p < 0.005.

    Journal: Current Issues in Molecular Biology

    Article Title: Extremophilic Solutions: The Role of Deinoxanthin in Counteracting UV-Induced Skin Harm

    doi: 10.3390/cimb45100528

    Figure Lengend Snippet: Activity of tyrosinase in HFF-1 cells exposed to UVA ( A ) and UVB ( B ) radiation was determined after treatment with varying concentrations of DNX. Statistical significance in this figure indicates the observed differences between the control group and the groups treated with varying concentrations of DNX and VitC, all subjected to the same UV dosage levels. The mean percentages ± s.e.m. are shown ( n = 6). * p < 0.05; ** p < 0.001; *** p < 0.005.

    Article Snippet: The human foreskin fibroblast cell line HFF-1 was obtained from ATCC (American Type Culture Collection, Manassas, VA, USA, LGC Promochem, Teddington, UK).

    Techniques: Activity Assay

    Activity of SOD in HFF-1 cell after UVA and UVB irradiation with different concentrations of DNX and VitC. Values are represented as mean ± standard error of mean. a p < 0.05 vs. control group. b p < 0.05 vs. UVA group. c p < 0.05 VitC-treated + UVA group. d p < 0.05 UVB group. e p < 0.05 VitC-treated + UVB group.

    Journal: Current Issues in Molecular Biology

    Article Title: Extremophilic Solutions: The Role of Deinoxanthin in Counteracting UV-Induced Skin Harm

    doi: 10.3390/cimb45100528

    Figure Lengend Snippet: Activity of SOD in HFF-1 cell after UVA and UVB irradiation with different concentrations of DNX and VitC. Values are represented as mean ± standard error of mean. a p < 0.05 vs. control group. b p < 0.05 vs. UVA group. c p < 0.05 VitC-treated + UVA group. d p < 0.05 UVB group. e p < 0.05 VitC-treated + UVB group.

    Article Snippet: The human foreskin fibroblast cell line HFF-1 was obtained from ATCC (American Type Culture Collection, Manassas, VA, USA, LGC Promochem, Teddington, UK).

    Techniques: Activity Assay, Irradiation

    ( A ) ROS level in HFF-1 cells post UVA and UVB exposure, influenced by varying concentrations of DNX ( B ) MDA in HFF-1 cell after UVA and UVB irradiation with varying concentrations of DNX. Values are represented as mean ± standard error of mean. a p < 0.05 vs. control group. b p < 0.05 vs. UVA group. c p < 0.05 VitC-treated + UVA group. d p < 0.05 UVB group. e p < 0.05 VitC-treated + UVB group.

    Journal: Current Issues in Molecular Biology

    Article Title: Extremophilic Solutions: The Role of Deinoxanthin in Counteracting UV-Induced Skin Harm

    doi: 10.3390/cimb45100528

    Figure Lengend Snippet: ( A ) ROS level in HFF-1 cells post UVA and UVB exposure, influenced by varying concentrations of DNX ( B ) MDA in HFF-1 cell after UVA and UVB irradiation with varying concentrations of DNX. Values are represented as mean ± standard error of mean. a p < 0.05 vs. control group. b p < 0.05 vs. UVA group. c p < 0.05 VitC-treated + UVA group. d p < 0.05 UVB group. e p < 0.05 VitC-treated + UVB group.

    Article Snippet: The human foreskin fibroblast cell line HFF-1 was obtained from ATCC (American Type Culture Collection, Manassas, VA, USA, LGC Promochem, Teddington, UK).

    Techniques: Irradiation

    Hydroxyproline formation in HFF-1 cell after UVA and UVB irradiation with varying concentrations of DNX and VitC. Values are represented as mean ± standard error of mean. a p < 0.05 vs. control group. b p < 0.05 vs. UVA group. c p < 0.05 VitC-treated + UVA group. d p < 0.05 UVB group. e p < 0.05 VitC-treated + UVB group.

    Journal: Current Issues in Molecular Biology

    Article Title: Extremophilic Solutions: The Role of Deinoxanthin in Counteracting UV-Induced Skin Harm

    doi: 10.3390/cimb45100528

    Figure Lengend Snippet: Hydroxyproline formation in HFF-1 cell after UVA and UVB irradiation with varying concentrations of DNX and VitC. Values are represented as mean ± standard error of mean. a p < 0.05 vs. control group. b p < 0.05 vs. UVA group. c p < 0.05 VitC-treated + UVA group. d p < 0.05 UVB group. e p < 0.05 VitC-treated + UVB group.

    Article Snippet: The human foreskin fibroblast cell line HFF-1 was obtained from ATCC (American Type Culture Collection, Manassas, VA, USA, LGC Promochem, Teddington, UK).

    Techniques: Irradiation

    Impact of DNX on the wound healing response in UVA-exposed HFF-1 cells. ( A ) DNX counteracts the impediments in wound healing caused by UVA exposure. Upon reaching confluency, cells were scratched using a pipette tip and subsequently pretreated with DNX and VitC before UVA exposure. Inverted images (40× magnifications, 400 µm scale bar) of the scratched HFF-1 cells were captured at the 0 and 24 h marks post irradiation. ( B ) The wound healing assay’s graph, representing % wound closure, was generated by analyzing the captured inverted images through the Image-Pro Plus 6.0 Software. Data are expressed as the mean ± standard deviation of three independent experiments. Ns: non-significance, * p < 0.05.

    Journal: Current Issues in Molecular Biology

    Article Title: Extremophilic Solutions: The Role of Deinoxanthin in Counteracting UV-Induced Skin Harm

    doi: 10.3390/cimb45100528

    Figure Lengend Snippet: Impact of DNX on the wound healing response in UVA-exposed HFF-1 cells. ( A ) DNX counteracts the impediments in wound healing caused by UVA exposure. Upon reaching confluency, cells were scratched using a pipette tip and subsequently pretreated with DNX and VitC before UVA exposure. Inverted images (40× magnifications, 400 µm scale bar) of the scratched HFF-1 cells were captured at the 0 and 24 h marks post irradiation. ( B ) The wound healing assay’s graph, representing % wound closure, was generated by analyzing the captured inverted images through the Image-Pro Plus 6.0 Software. Data are expressed as the mean ± standard deviation of three independent experiments. Ns: non-significance, * p < 0.05.

    Article Snippet: The human foreskin fibroblast cell line HFF-1 was obtained from ATCC (American Type Culture Collection, Manassas, VA, USA, LGC Promochem, Teddington, UK).

    Techniques: Transferring, Irradiation, Generated, Software, Standard Deviation

    Effect of DNX on scratch wound healing in UVB-irradiated HFF-1 cells. ( A ) DNX rescues the UVB-induced wound-healing defect. Confluent cells were mechanically scratched with a pipette tip and pretreated with DNX and VitC prior to UVB irradiation. Invert micrographs (40× magnifications, 400 µm scale bar) of scratched HFF-1 cells were taken at 0 and 24 h following irradiation. ( B ) In the wound healing assay, the graph of % wound closure was derived from the assessment of inverted micrographs using Image-Pro Plus 6.0 Software. Data are expressed as the mean ± standard deviation of three independent experiments. ns: non-significance, * p < 0.05.

    Journal: Current Issues in Molecular Biology

    Article Title: Extremophilic Solutions: The Role of Deinoxanthin in Counteracting UV-Induced Skin Harm

    doi: 10.3390/cimb45100528

    Figure Lengend Snippet: Effect of DNX on scratch wound healing in UVB-irradiated HFF-1 cells. ( A ) DNX rescues the UVB-induced wound-healing defect. Confluent cells were mechanically scratched with a pipette tip and pretreated with DNX and VitC prior to UVB irradiation. Invert micrographs (40× magnifications, 400 µm scale bar) of scratched HFF-1 cells were taken at 0 and 24 h following irradiation. ( B ) In the wound healing assay, the graph of % wound closure was derived from the assessment of inverted micrographs using Image-Pro Plus 6.0 Software. Data are expressed as the mean ± standard deviation of three independent experiments. ns: non-significance, * p < 0.05.

    Article Snippet: The human foreskin fibroblast cell line HFF-1 was obtained from ATCC (American Type Culture Collection, Manassas, VA, USA, LGC Promochem, Teddington, UK).

    Techniques: Irradiation, Transferring, Wound Healing Assay, Derivative Assay, Software, Standard Deviation