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human foreskin fibroblasts hff  (ATCC)


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    ATCC human foreskin fibroblasts hff
    Human Foreskin Fibroblasts Hff, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1579 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/human+foreskin+fibroblast+hff+1/HFF-1/pmc13092094-59-11-17
    Average 99 stars, based on 1579 article reviews
    human foreskin fibroblasts hff - by Bioz Stars, 2026-09
    99/100 stars

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    Related Articles

    Cell Culture:

    Article Title: Development of New Drug Against Multidrug-Resistant Candidozyma ( Candida ) auris by Mining the Genome of Marine Bacteria Vibrio sp. IRMCESH58L.
    Article Snippet: .. In our study, Human Foreskin Fibroblast (HFF‐1) (ATCC® SCR‐C‐1041TM, Manassas, VA, USA) was used post‐ exposure to assess the cytotoxicity of IRMCESH58L 24 h cultured broth. .. The HFF‐1 cells were seeded in a 96‐well plate with a seeding density of 13,000 cells/mL for 24 h before applying the control to bacteria‐free Tryptic Soy Broth (TSB) (control) (MOLEQULE‐ON, Auckland, New Zealand), and IRMCESH58L broths were added to the cells.

    Article Title: Development of New Drug Against Multidrug-Resistant Candidozyma ( Candida ) auris by Mining the Genome of Marine Bacteria Vibrio sp. IRMCESH58L
    Article Snippet: .. In our study, Human Foreskin Fibroblast (HFF-1) (ATCC ® SCR-C-1041TM, Manassas, VA, USA) was used post-exposure to assess the cytotoxicity of IRMCESH58L 24 h cultured broth. .. The HFF-1 cells were seeded in a 96-well plate with a seeding density of 13,000 cells/mL for 24 h before applying the control to bacteria-free Tryptic Soy Broth (TSB) (control) (MOLEQULE-ON, Auckland, New Zealand), and IRMCESH58L broths were added to the cells.

    Incubation:

    Article Title: Multi-stimuli-responsive degradable boronic ester-crosslinked e-spun nanofiber wound dressings.
    Article Snippet: .. Furthermore, the biocompatibility of the mats was tested with human foreskin fibroblast HFF-1, along with human Fig. 9 Growth of E. coli ATCC 25922 (a)–(c) and S. aureus ATCC 29213 (d)–(f) incubated with no mats (e.g. bacteria alone) (a) and (b), BE-PVA mats (b) and (e), and BE-PVA/LF (0.005 wt%) at pH = 5.4, 7.4, and 8.4 over 72 h, determined by the suspension method. ..

    Bacteria:

    Article Title: Multi-stimuli-responsive degradable boronic ester-crosslinked e-spun nanofiber wound dressings.
    Article Snippet: .. Furthermore, the biocompatibility of the mats was tested with human foreskin fibroblast HFF-1, along with human Fig. 9 Growth of E. coli ATCC 25922 (a)–(c) and S. aureus ATCC 29213 (d)–(f) incubated with no mats (e.g. bacteria alone) (a) and (b), BE-PVA mats (b) and (e), and BE-PVA/LF (0.005 wt%) at pH = 5.4, 7.4, and 8.4 over 72 h, determined by the suspension method. ..

    Suspension:

    Article Title: Multi-stimuli-responsive degradable boronic ester-crosslinked e-spun nanofiber wound dressings.
    Article Snippet: .. Furthermore, the biocompatibility of the mats was tested with human foreskin fibroblast HFF-1, along with human Fig. 9 Growth of E. coli ATCC 25922 (a)–(c) and S. aureus ATCC 29213 (d)–(f) incubated with no mats (e.g. bacteria alone) (a) and (b), BE-PVA mats (b) and (e), and BE-PVA/LF (0.005 wt%) at pH = 5.4, 7.4, and 8.4 over 72 h, determined by the suspension method. ..

    other:

    Article Title: Placing purines in precision medicine: Targeting a metabolic reliance in KRAS -mutant tumors
    Article Snippet: Human Foreskin Fibroblast (HFF-1) , ATCC , Cat# SCRC-1041.



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    human foreskin fibroblasts hff  (ATCC)
    99
    ATCC human foreskin fibroblasts hff
    Human Foreskin Fibroblasts Hff, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/human+foreskin+fibroblast+hff+1/HFF-1/pmc13092094-59-11-17
    Average 99 stars, based on 1 article reviews
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    human foreskin fibroblasts  (ATCC)
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    human foreskin fibroblast cell line hff  (ATCC)
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    ATCC human foreskin fibroblast cell line hff
    Expression of EpCAM on cell lines of SCC-UADT, HNSCC-associated fibroblasts, and normal fibroblasts. A Representative histogram and quantitative data on the percentage of EpCAM-positive cells as well as on the expression level of EpCAM of the SCC-UADT cell lines KYSE-30 (ESCC) and FaDu (HNSCC), the HNSCC-associated fibroblast cell line CAF-4, and the normal fibroblast cell <t>line</t> <t>HFF-1</t> as assessed by flow cytometry upon immunostaining with the AlexaFluor488-labeled anti-EpCAM antibody VU1D9 (high EpCAM-affinity) (mean ± SEM for n = 4; * p < .05 vs. CAF; # p < .05 vs. HFF; § p < .05 vs. KYSE-30; & p < .05 vs. FaDu). B Representative histogram and quantitative data on the percentage of EpCAM-positive cells as well as on the expression level of EpCAM of the SCC-UADT cell lines KYSE-30 and FaDu, the HNSCC-associated fibroblast cell line CAF-4, and the normal fibroblast cell line HFF-1 as assessed by flow cytometry upon immunostaining with the AlexaFluor488-labeled anti-EpCAM antibody MT201 (intermediate EpCAM-affinity; clinically validated) (mean ± SEM for n = 4; * p < .05 vs. CAF; # p < .05 vs. HFF; § p < .05 vs. KYSE-30; & p < .05 vs. FaDu)
    Human Foreskin Fibroblast Cell Line Hff, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/human+foreskin+fibroblast+hff+1/HFF-1/pmc13200314-41-0-9
    Average 99 stars, based on 1 article reviews
    human foreskin fibroblast cell line hff - by Bioz Stars, 2026-09
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    human foreskin fibroblast hff 1  (ATCC)
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    ATCC human foreskin fibroblast hff 1
    Cytotoxicity assay of ZnFe 2 O 4 /HNT formulations <t>treated</t> <t>HFF-1</t> cells. Cell viability (%) of HeLa cells following treatment with nanocarrier formulations for ( a ) 24 h, ( b ) 48 h, and ( c ) 72 h, as determined by the MTT assay. Cells were exposed to increasing concentrations of the indicated formulations, including ZnFe 2 O 4 /HNT, ZnFe 2 O 4 /HNT/Cp, ZnFe 2 O 4 /HNT/Cp/FA/PEG, ZnFe 2 O 4 /HNT/Cbpt, Cbpt, and Cp. Statistical significance is indicated as ns: not significant,* p ≤ 0.05, ** p ≤ 0.01, *** p ≤ 0.001, **** p ≤ 0.0001.
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    primary human fetal foreskin fibroblasts  (ATCC)
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    ATCC primary human fetal foreskin fibroblasts
    Cytotoxicity assay of ZnFe 2 O 4 /HNT formulations <t>treated</t> <t>HFF-1</t> cells. Cell viability (%) of HeLa cells following treatment with nanocarrier formulations for ( a ) 24 h, ( b ) 48 h, and ( c ) 72 h, as determined by the MTT assay. Cells were exposed to increasing concentrations of the indicated formulations, including ZnFe 2 O 4 /HNT, ZnFe 2 O 4 /HNT/Cp, ZnFe 2 O 4 /HNT/Cp/FA/PEG, ZnFe 2 O 4 /HNT/Cbpt, Cbpt, and Cp. Statistical significance is indicated as ns: not significant,* p ≤ 0.05, ** p ≤ 0.01, *** p ≤ 0.001, **** p ≤ 0.0001.
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    Image Search Results


    Expression of EpCAM on cell lines of SCC-UADT, HNSCC-associated fibroblasts, and normal fibroblasts. A Representative histogram and quantitative data on the percentage of EpCAM-positive cells as well as on the expression level of EpCAM of the SCC-UADT cell lines KYSE-30 (ESCC) and FaDu (HNSCC), the HNSCC-associated fibroblast cell line CAF-4, and the normal fibroblast cell line HFF-1 as assessed by flow cytometry upon immunostaining with the AlexaFluor488-labeled anti-EpCAM antibody VU1D9 (high EpCAM-affinity) (mean ± SEM for n = 4; * p < .05 vs. CAF; # p < .05 vs. HFF; § p < .05 vs. KYSE-30; & p < .05 vs. FaDu). B Representative histogram and quantitative data on the percentage of EpCAM-positive cells as well as on the expression level of EpCAM of the SCC-UADT cell lines KYSE-30 and FaDu, the HNSCC-associated fibroblast cell line CAF-4, and the normal fibroblast cell line HFF-1 as assessed by flow cytometry upon immunostaining with the AlexaFluor488-labeled anti-EpCAM antibody MT201 (intermediate EpCAM-affinity; clinically validated) (mean ± SEM for n = 4; * p < .05 vs. CAF; # p < .05 vs. HFF; § p < .05 vs. KYSE-30; & p < .05 vs. FaDu)

    Journal: BMC Cancer

    Article Title: Targeting EpCAM expression via near-infrared fluorescent antibodies enables microscopic delineation of primary and recurrent HNSCC

    doi: 10.1186/s12885-026-16172-2

    Figure Lengend Snippet: Expression of EpCAM on cell lines of SCC-UADT, HNSCC-associated fibroblasts, and normal fibroblasts. A Representative histogram and quantitative data on the percentage of EpCAM-positive cells as well as on the expression level of EpCAM of the SCC-UADT cell lines KYSE-30 (ESCC) and FaDu (HNSCC), the HNSCC-associated fibroblast cell line CAF-4, and the normal fibroblast cell line HFF-1 as assessed by flow cytometry upon immunostaining with the AlexaFluor488-labeled anti-EpCAM antibody VU1D9 (high EpCAM-affinity) (mean ± SEM for n = 4; * p < .05 vs. CAF; # p < .05 vs. HFF; § p < .05 vs. KYSE-30; & p < .05 vs. FaDu). B Representative histogram and quantitative data on the percentage of EpCAM-positive cells as well as on the expression level of EpCAM of the SCC-UADT cell lines KYSE-30 and FaDu, the HNSCC-associated fibroblast cell line CAF-4, and the normal fibroblast cell line HFF-1 as assessed by flow cytometry upon immunostaining with the AlexaFluor488-labeled anti-EpCAM antibody MT201 (intermediate EpCAM-affinity; clinically validated) (mean ± SEM for n = 4; * p < .05 vs. CAF; # p < .05 vs. HFF; § p < .05 vs. KYSE-30; & p < .05 vs. FaDu)

    Article Snippet: Human foreskin fibroblast cell line HFF-1 was purchased from ATCC (Manassas, USA; SCRC-1041).

    Techniques: Expressing, Flow Cytometry, Immunostaining, Labeling

    Cytotoxicity assay of ZnFe 2 O 4 /HNT formulations treated HFF-1 cells. Cell viability (%) of HeLa cells following treatment with nanocarrier formulations for ( a ) 24 h, ( b ) 48 h, and ( c ) 72 h, as determined by the MTT assay. Cells were exposed to increasing concentrations of the indicated formulations, including ZnFe 2 O 4 /HNT, ZnFe 2 O 4 /HNT/Cp, ZnFe 2 O 4 /HNT/Cp/FA/PEG, ZnFe 2 O 4 /HNT/Cbpt, Cbpt, and Cp. Statistical significance is indicated as ns: not significant,* p ≤ 0.05, ** p ≤ 0.01, *** p ≤ 0.001, **** p ≤ 0.0001.

    Journal: International Journal of Molecular Sciences

    Article Title: Zinc Ferrite-Integrated Halloysite Nanotubes as a Platform for Folate-Mediated Targeted Cisplatin Delivery

    doi: 10.3390/ijms27104284

    Figure Lengend Snippet: Cytotoxicity assay of ZnFe 2 O 4 /HNT formulations treated HFF-1 cells. Cell viability (%) of HeLa cells following treatment with nanocarrier formulations for ( a ) 24 h, ( b ) 48 h, and ( c ) 72 h, as determined by the MTT assay. Cells were exposed to increasing concentrations of the indicated formulations, including ZnFe 2 O 4 /HNT, ZnFe 2 O 4 /HNT/Cp, ZnFe 2 O 4 /HNT/Cp/FA/PEG, ZnFe 2 O 4 /HNT/Cbpt, Cbpt, and Cp. Statistical significance is indicated as ns: not significant,* p ≤ 0.05, ** p ≤ 0.01, *** p ≤ 0.001, **** p ≤ 0.0001.

    Article Snippet: The cervical cancer cell line HeLa (ATCC ® CCL-2TM, ATCC, Manassas, VA, USA) and the human foreskin fibroblast HFF-1 (ATCC ® SCR-C-1041TM, ATCC, Manassas, VA, USA) were purchased from the American Type Culture Collection (ATCC).

    Techniques: Cytotoxicity Assay, MTT Assay