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human foreskin fibroblasts hff  (ATCC)


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    Structured Review

    ATCC human foreskin fibroblasts hff
    Human Foreskin Fibroblasts Hff, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1582 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/hff-1/HFF-1/pmc13092094-59-11-17
    Average 99 stars, based on 1582 article reviews
    human foreskin fibroblasts hff - by Bioz Stars, 2026-10
    99/100 stars

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    Related Articles

    Cell Culture:

    Article Title: Extracellular matrix abnormalities in Hutchinson–Gilford progeria fibroblasts: a specific defect in collagen IV and basement membrane architecture?
    Article Snippet: ance, a recognized feature of aged human skin [33] . Patient fibroblasts were established by outgrowth from skin biopsy as previously described [34] . Neonatal foreskin fibroblasts from Invitrogen and ATCC (HFF-1, SCRC-1041) were used as control line #1 and #2, respectively. Fibroblasts were cultured in DMEM/F12 supplemented with 10% FBS and 1% penicillin/streptomycin and controlled for mycoplasma

    Control:

    Article Title: Extracellular matrix abnormalities in Hutchinson–Gilford progeria fibroblasts: a specific defect in collagen IV and basement membrane architecture?
    Article Snippet: ance, a recognized feature of aged human skin [33] . Patient fibroblasts were established by outgrowth from skin biopsy as previously described [34] . Neonatal foreskin fibroblasts from Invitrogen and ATCC (HFF-1, SCRC-1041) were used as control line #1 and #2, respectively. Fibroblasts were cultured in DMEM/F12 supplemented with 10% FBS and 1% penicillin/streptomycin and controlled for mycoplasma

    Positive Control:

    Article Title: Extracellular matrix abnormalities in Hutchinson–Gilford progeria fibroblasts: a specific defect in collagen IV and basement membrane architecture?
    Article Snippet: ance, a recognized feature of aged human skin [33] . Patient fibroblasts were established by outgrowth from skin biopsy as previously described [34] . Neonatal foreskin fibroblasts from Invitrogen and ATCC (HFF-1, SCRC-1041) were used as control line #1 and #2, respectively. Fibroblasts were cultured in DMEM/F12 supplemented with 10% FBS and 1% penicillin/streptomycin and controlled for mycoplasma

    Negative Control:

    Article Title: Extracellular matrix abnormalities in Hutchinson–Gilford progeria fibroblasts: a specific defect in collagen IV and basement membrane architecture?
    Article Snippet: ance, a recognized feature of aged human skin [33] . Patient fibroblasts were established by outgrowth from skin biopsy as previously described [34] . Neonatal foreskin fibroblasts from Invitrogen and ATCC (HFF-1, SCRC-1041) were used as control line #1 and #2, respectively. Fibroblasts were cultured in DMEM/F12 supplemented with 10% FBS and 1% penicillin/streptomycin and controlled for mycoplasma

    Mutagenesis:

    Article Title: Extracellular matrix abnormalities in Hutchinson–Gilford progeria fibroblasts: a specific defect in collagen IV and basement membrane architecture?
    Article Snippet: ance, a recognized feature of aged human skin [33] . Patient fibroblasts were established by outgrowth from skin biopsy as previously described [34] . Neonatal foreskin fibroblasts from Invitrogen and ATCC (HFF-1, SCRC-1041) were used as control line #1 and #2, respectively. Fibroblasts were cultured in DMEM/F12 supplemented with 10% FBS and 1% penicillin/streptomycin and controlled for mycoplasma

    Expressing:

    Article Title: Extracellular matrix abnormalities in Hutchinson–Gilford progeria fibroblasts: a specific defect in collagen IV and basement membrane architecture?
    Article Snippet: ance, a recognized feature of aged human skin [33] . Patient fibroblasts were established by outgrowth from skin biopsy as previously described [34] . Neonatal foreskin fibroblasts from Invitrogen and ATCC (HFF-1, SCRC-1041) were used as control line #1 and #2, respectively. Fibroblasts were cultured in DMEM/F12 supplemented with 10% FBS and 1% penicillin/streptomycin and controlled for mycoplasma

    Generated:

    Article Title: Extracellular matrix abnormalities in Hutchinson–Gilford progeria fibroblasts: a specific defect in collagen IV and basement membrane architecture?
    Article Snippet: ance, a recognized feature of aged human skin [33] . Patient fibroblasts were established by outgrowth from skin biopsy as previously described [34] . Neonatal foreskin fibroblasts from Invitrogen and ATCC (HFF-1, SCRC-1041) were used as control line #1 and #2, respectively. Fibroblasts were cultured in DMEM/F12 supplemented with 10% FBS and 1% penicillin/streptomycin and controlled for mycoplasma

    Clone Assay:

    Article Title: Extracellular matrix abnormalities in Hutchinson–Gilford progeria fibroblasts: a specific defect in collagen IV and basement membrane architecture?
    Article Snippet: ance, a recognized feature of aged human skin [33] . Patient fibroblasts were established by outgrowth from skin biopsy as previously described [34] . Neonatal foreskin fibroblasts from Invitrogen and ATCC (HFF-1, SCRC-1041) were used as control line #1 and #2, respectively. Fibroblasts were cultured in DMEM/F12 supplemented with 10% FBS and 1% penicillin/streptomycin and controlled for mycoplasma

    Stable Transfection:

    Article Title: Extracellular matrix abnormalities in Hutchinson–Gilford progeria fibroblasts: a specific defect in collagen IV and basement membrane architecture?
    Article Snippet: ance, a recognized feature of aged human skin [33] . Patient fibroblasts were established by outgrowth from skin biopsy as previously described [34] . Neonatal foreskin fibroblasts from Invitrogen and ATCC (HFF-1, SCRC-1041) were used as control line #1 and #2, respectively. Fibroblasts were cultured in DMEM/F12 supplemented with 10% FBS and 1% penicillin/streptomycin and controlled for mycoplasma

    Transduction:

    Article Title: Extracellular matrix abnormalities in Hutchinson–Gilford progeria fibroblasts: a specific defect in collagen IV and basement membrane architecture?
    Article Snippet: ance, a recognized feature of aged human skin [33] . Patient fibroblasts were established by outgrowth from skin biopsy as previously described [34] . Neonatal foreskin fibroblasts from Invitrogen and ATCC (HFF-1, SCRC-1041) were used as control line #1 and #2, respectively. Fibroblasts were cultured in DMEM/F12 supplemented with 10% FBS and 1% penicillin/streptomycin and controlled for mycoplasma

    Mouse Assay:

    Article Title: Extracellular matrix abnormalities in Hutchinson–Gilford progeria fibroblasts: a specific defect in collagen IV and basement membrane architecture?
    Article Snippet: ance, a recognized feature of aged human skin [33] . Patient fibroblasts were established by outgrowth from skin biopsy as previously described [34] . Neonatal foreskin fibroblasts from Invitrogen and ATCC (HFF-1, SCRC-1041) were used as control line #1 and #2, respectively. Fibroblasts were cultured in DMEM/F12 supplemented with 10% FBS and 1% penicillin/streptomycin and controlled for mycoplasma

    Plasmid Preparation:

    Article Title: Extracellular matrix abnormalities in Hutchinson–Gilford progeria fibroblasts: a specific defect in collagen IV and basement membrane architecture?
    Article Snippet: ance, a recognized feature of aged human skin [33] . Patient fibroblasts were established by outgrowth from skin biopsy as previously described [34] . Neonatal foreskin fibroblasts from Invitrogen and ATCC (HFF-1, SCRC-1041) were used as control line #1 and #2, respectively. Fibroblasts were cultured in DMEM/F12 supplemented with 10% FBS and 1% penicillin/streptomycin and controlled for mycoplasma

    Transfection:

    Article Title: Extracellular matrix abnormalities in Hutchinson–Gilford progeria fibroblasts: a specific defect in collagen IV and basement membrane architecture?
    Article Snippet: ance, a recognized feature of aged human skin [33] . Patient fibroblasts were established by outgrowth from skin biopsy as previously described [34] . Neonatal foreskin fibroblasts from Invitrogen and ATCC (HFF-1, SCRC-1041) were used as control line #1 and #2, respectively. Fibroblasts were cultured in DMEM/F12 supplemented with 10% FBS and 1% penicillin/streptomycin and controlled for mycoplasma

    Irradiation:

    Article Title: Extracellular matrix abnormalities in Hutchinson–Gilford progeria fibroblasts: a specific defect in collagen IV and basement membrane architecture?
    Article Snippet: ance, a recognized feature of aged human skin [33] . Patient fibroblasts were established by outgrowth from skin biopsy as previously described [34] . Neonatal foreskin fibroblasts from Invitrogen and ATCC (HFF-1, SCRC-1041) were used as control line #1 and #2, respectively. Fibroblasts were cultured in DMEM/F12 supplemented with 10% FBS and 1% penicillin/streptomycin and controlled for mycoplasma

    Modification:

    Article Title: Extracellular matrix abnormalities in Hutchinson–Gilford progeria fibroblasts: a specific defect in collagen IV and basement membrane architecture?
    Article Snippet: ance, a recognized feature of aged human skin [33] . Patient fibroblasts were established by outgrowth from skin biopsy as previously described [34] . Neonatal foreskin fibroblasts from Invitrogen and ATCC (HFF-1, SCRC-1041) were used as control line #1 and #2, respectively. Fibroblasts were cultured in DMEM/F12 supplemented with 10% FBS and 1% penicillin/streptomycin and controlled for mycoplasma



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