cell lines primary human foreskin fibroblasts hff atcc scrc 1041  (ATCC)


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    ATCC cell lines primary human foreskin fibroblasts hff atcc scrc 1041
    Cell Lines Primary Human Foreskin Fibroblasts Hff Atcc Scrc 1041, 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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    cell lines human foreskin fibroblast hff atcc hff 1 atcc scrc 1041  (ATCC)


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    ATCC cell lines human foreskin fibroblast hff atcc hff 1 atcc scrc 1041
    Cell Lines Human Foreskin Fibroblast Hff Atcc Hff 1 Atcc Scrc 1041, 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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    cytotoxicity human foreskin fibroblasts hff 1 cell line  (ATCC)


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    ATCC cytotoxicity human foreskin fibroblasts hff 1 cell line
    Cytotoxicity 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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    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 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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    human foreskin fibroblast cell line hff - by Bioz Stars, 2024-02
    86/100 stars

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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

    human foreskin fibroblast cell line hff  (ATCC)


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    ATCC human foreskin fibroblast cell line hff
    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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    human foreskin fibroblast cell line hff 1  (ATCC)


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    ATCC human foreskin fibroblast cell line hff 1
    Human Foreskin Fibroblast Cell Line Hff 1, 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 1 hff 1 cell line  (ATCC)


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    ATCC human foreskin fibroblast 1 hff 1 cell line
    Human Foreskin Fibroblast 1 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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    human foreskin fibroblast 1 hff 1 cell line  (ATCC)


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    ATCC human foreskin fibroblast 1 hff 1 cell line
    Human Foreskin Fibroblast 1 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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    human foreskin fibroblast cell line hff 1  (ATCC)


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    ATCC human foreskin fibroblast cell line hff 1
    Human Foreskin Fibroblast Cell Line Hff 1, 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 cell lines primary human foreskin fibroblasts hff atcc scrc 1041
    Cell Lines Primary Human Foreskin Fibroblasts Hff Atcc Scrc 1041, 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 cell lines human foreskin fibroblast hff atcc hff 1 atcc scrc 1041
    Cell Lines Human Foreskin Fibroblast Hff Atcc Hff 1 Atcc Scrc 1041, 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 cytotoxicity human foreskin fibroblasts hff 1 cell line
    Cytotoxicity 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 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 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 human foreskin fibroblast cell line hff 1
    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 1, 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 1 hff 1 cell line
    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 1 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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    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

    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