Review



fibroblast culture medium fcm  (Lonza)


Bioz Verified Symbol Lonza is a verified supplier
Bioz Manufacturer Symbol Lonza manufactures this product  
  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
    • 90
      Buy from Supplier

    Structured Review

    Lonza fibroblast culture medium fcm
    Human <t>fibroblast</t> seeding on the hypodermal side of d-NACs. (A) H&E staining of adherent human fibroblasts (arrows) on the acellular hypodermal side and, in some locations, adherent to the epidermal side of d-NACs after 7 days of static culture (scale bar = 200 μm). (A’) Higher magnification of the H&E-stained section highlighting adherent fibroblasts forming several cell layers on the hypodermal side of the scaffold (scale bar = 100 μm). (B) Live/dead staining of seeded fibroblasts shows a high viability on day 7 of the culture on the scaffold (living cells = green and dead cells = red) (scale bar = 500 μm). (C) Cell viability of the seeded dermis: ECM- red and control wells- blue. The results are expressed as the mean cell viability. Error bars: SD; ns = not significant. (D) A PrestoBlue cell viability assay realized on seeded d-NACs (red, n = 3) and control culture wells (blue, n = 3) attests the biocompatibility of the produced scaffolds by the increase in metabolic activity during the 7 days of culture. The results are expressed as the mean fluorescence intensity. Error bars: SD; ** p < 0.01; ns = not significant.
    Fibroblast Culture Medium Fcm, supplied by Lonza, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/fibroblast+culture+medium+fcm/pmc10902434-153-5-13?v=Lonza
    Average 90 stars, based on 1 article reviews
    fibroblast culture medium fcm - by Bioz Stars, 2026-07
    90/100 stars

    Images

    1) Product Images from "Reconstruction of the human nipple–areolar complex: a tissue engineering approach"

    Article Title: Reconstruction of the human nipple–areolar complex: a tissue engineering approach

    Journal: Frontiers in Bioengineering and Biotechnology

    doi: 10.3389/fbioe.2023.1295075

    Human fibroblast seeding on the hypodermal side of d-NACs. (A) H&E staining of adherent human fibroblasts (arrows) on the acellular hypodermal side and, in some locations, adherent to the epidermal side of d-NACs after 7 days of static culture (scale bar = 200 μm). (A’) Higher magnification of the H&E-stained section highlighting adherent fibroblasts forming several cell layers on the hypodermal side of the scaffold (scale bar = 100 μm). (B) Live/dead staining of seeded fibroblasts shows a high viability on day 7 of the culture on the scaffold (living cells = green and dead cells = red) (scale bar = 500 μm). (C) Cell viability of the seeded dermis: ECM- red and control wells- blue. The results are expressed as the mean cell viability. Error bars: SD; ns = not significant. (D) A PrestoBlue cell viability assay realized on seeded d-NACs (red, n = 3) and control culture wells (blue, n = 3) attests the biocompatibility of the produced scaffolds by the increase in metabolic activity during the 7 days of culture. The results are expressed as the mean fluorescence intensity. Error bars: SD; ** p < 0.01; ns = not significant.
    Figure Legend Snippet: Human fibroblast seeding on the hypodermal side of d-NACs. (A) H&E staining of adherent human fibroblasts (arrows) on the acellular hypodermal side and, in some locations, adherent to the epidermal side of d-NACs after 7 days of static culture (scale bar = 200 μm). (A’) Higher magnification of the H&E-stained section highlighting adherent fibroblasts forming several cell layers on the hypodermal side of the scaffold (scale bar = 100 μm). (B) Live/dead staining of seeded fibroblasts shows a high viability on day 7 of the culture on the scaffold (living cells = green and dead cells = red) (scale bar = 500 μm). (C) Cell viability of the seeded dermis: ECM- red and control wells- blue. The results are expressed as the mean cell viability. Error bars: SD; ns = not significant. (D) A PrestoBlue cell viability assay realized on seeded d-NACs (red, n = 3) and control culture wells (blue, n = 3) attests the biocompatibility of the produced scaffolds by the increase in metabolic activity during the 7 days of culture. The results are expressed as the mean fluorescence intensity. Error bars: SD; ** p < 0.01; ns = not significant.

    Techniques Used: Staining, Control, Viability Assay, Produced, Activity Assay, Fluorescence


    Figure Legend Snippet:

    Techniques Used: Immunofluorescence, Immunohistochemistry, Immunopeptidomics, Saline, Standard Deviation



    Similar Products

    fibroblast culture medium fcm  (Lonza)
    90
    Lonza fibroblast culture medium fcm
    Human <t>fibroblast</t> seeding on the hypodermal side of d-NACs. (A) H&E staining of adherent human fibroblasts (arrows) on the acellular hypodermal side and, in some locations, adherent to the epidermal side of d-NACs after 7 days of static culture (scale bar = 200 μm). (A’) Higher magnification of the H&E-stained section highlighting adherent fibroblasts forming several cell layers on the hypodermal side of the scaffold (scale bar = 100 μm). (B) Live/dead staining of seeded fibroblasts shows a high viability on day 7 of the culture on the scaffold (living cells = green and dead cells = red) (scale bar = 500 μm). (C) Cell viability of the seeded dermis: ECM- red and control wells- blue. The results are expressed as the mean cell viability. Error bars: SD; ns = not significant. (D) A PrestoBlue cell viability assay realized on seeded d-NACs (red, n = 3) and control culture wells (blue, n = 3) attests the biocompatibility of the produced scaffolds by the increase in metabolic activity during the 7 days of culture. The results are expressed as the mean fluorescence intensity. Error bars: SD; ** p < 0.01; ns = not significant.
    Fibroblast Culture Medium Fcm, supplied by Lonza, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/fibroblast+culture+medium+fcm/pmc10902434-153-5-13?v=Lonza
    Average 90 stars, based on 1 article reviews
    fibroblast culture medium fcm - by Bioz Stars, 2026-07
    90/100 stars
    		  Buy from Supplier
    fibroblast culture medium (fcm) dmem, high glucose, +glutamax  (Thermo Fisher)
    90
    Thermo Fisher fibroblast culture medium (fcm) dmem, high glucose, +glutamax
    Human <t>fibroblast</t> seeding on the hypodermal side of d-NACs. (A) H&E staining of adherent human fibroblasts (arrows) on the acellular hypodermal side and, in some locations, adherent to the epidermal side of d-NACs after 7 days of static culture (scale bar = 200 μm). (A’) Higher magnification of the H&E-stained section highlighting adherent fibroblasts forming several cell layers on the hypodermal side of the scaffold (scale bar = 100 μm). (B) Live/dead staining of seeded fibroblasts shows a high viability on day 7 of the culture on the scaffold (living cells = green and dead cells = red) (scale bar = 500 μm). (C) Cell viability of the seeded dermis: ECM- red and control wells- blue. The results are expressed as the mean cell viability. Error bars: SD; ns = not significant. (D) A PrestoBlue cell viability assay realized on seeded d-NACs (red, n = 3) and control culture wells (blue, n = 3) attests the biocompatibility of the produced scaffolds by the increase in metabolic activity during the 7 days of culture. The results are expressed as the mean fluorescence intensity. Error bars: SD; ** p < 0.01; ns = not significant.
    Fibroblast Culture Medium (Fcm) Dmem, High Glucose, +Glutamax, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/fibroblast+culture+medium+fcm/pm26439714-349-9-10?v=Thermo+Fisher
    Average 90 stars, based on 1 article reviews
    fibroblast culture medium (fcm) dmem, high glucose, +glutamax - by Bioz Stars, 2026-07
    90/100 stars
    		  Buy from Supplier
    fibroblast culture medium (fcm  (Thermo Fisher)
    90
    Thermo Fisher fibroblast culture medium (fcm
    Human <t>fibroblast</t> seeding on the hypodermal side of d-NACs. (A) H&E staining of adherent human fibroblasts (arrows) on the acellular hypodermal side and, in some locations, adherent to the epidermal side of d-NACs after 7 days of static culture (scale bar = 200 μm). (A’) Higher magnification of the H&E-stained section highlighting adherent fibroblasts forming several cell layers on the hypodermal side of the scaffold (scale bar = 100 μm). (B) Live/dead staining of seeded fibroblasts shows a high viability on day 7 of the culture on the scaffold (living cells = green and dead cells = red) (scale bar = 500 μm). (C) Cell viability of the seeded dermis: ECM- red and control wells- blue. The results are expressed as the mean cell viability. Error bars: SD; ns = not significant. (D) A PrestoBlue cell viability assay realized on seeded d-NACs (red, n = 3) and control culture wells (blue, n = 3) attests the biocompatibility of the produced scaffolds by the increase in metabolic activity during the 7 days of culture. The results are expressed as the mean fluorescence intensity. Error bars: SD; ** p < 0.01; ns = not significant.
    Fibroblast Culture Medium (Fcm, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/fibroblast+culture+medium+fcm/pm19494201-63-29-61?v=Thermo+Fisher
    Average 90 stars, based on 1 article reviews
    fibroblast culture medium (fcm - by Bioz Stars, 2026-07
    90/100 stars
    		  Buy from Supplier

    Image Search Results


    Human fibroblast seeding on the hypodermal side of d-NACs. (A) H&E staining of adherent human fibroblasts (arrows) on the acellular hypodermal side and, in some locations, adherent to the epidermal side of d-NACs after 7 days of static culture (scale bar = 200 μm). (A’) Higher magnification of the H&E-stained section highlighting adherent fibroblasts forming several cell layers on the hypodermal side of the scaffold (scale bar = 100 μm). (B) Live/dead staining of seeded fibroblasts shows a high viability on day 7 of the culture on the scaffold (living cells = green and dead cells = red) (scale bar = 500 μm). (C) Cell viability of the seeded dermis: ECM- red and control wells- blue. The results are expressed as the mean cell viability. Error bars: SD; ns = not significant. (D) A PrestoBlue cell viability assay realized on seeded d-NACs (red, n = 3) and control culture wells (blue, n = 3) attests the biocompatibility of the produced scaffolds by the increase in metabolic activity during the 7 days of culture. The results are expressed as the mean fluorescence intensity. Error bars: SD; ** p < 0.01; ns = not significant.

    Journal: Frontiers in Bioengineering and Biotechnology

    Article Title: Reconstruction of the human nipple–areolar complex: a tissue engineering approach

    doi: 10.3389/fbioe.2023.1295075

    Figure Lengend Snippet: Human fibroblast seeding on the hypodermal side of d-NACs. (A) H&E staining of adherent human fibroblasts (arrows) on the acellular hypodermal side and, in some locations, adherent to the epidermal side of d-NACs after 7 days of static culture (scale bar = 200 μm). (A’) Higher magnification of the H&E-stained section highlighting adherent fibroblasts forming several cell layers on the hypodermal side of the scaffold (scale bar = 100 μm). (B) Live/dead staining of seeded fibroblasts shows a high viability on day 7 of the culture on the scaffold (living cells = green and dead cells = red) (scale bar = 500 μm). (C) Cell viability of the seeded dermis: ECM- red and control wells- blue. The results are expressed as the mean cell viability. Error bars: SD; ns = not significant. (D) A PrestoBlue cell viability assay realized on seeded d-NACs (red, n = 3) and control culture wells (blue, n = 3) attests the biocompatibility of the produced scaffolds by the increase in metabolic activity during the 7 days of culture. The results are expressed as the mean fluorescence intensity. Error bars: SD; ** p < 0.01; ns = not significant.

    Article Snippet: HFs were mixed in a fibroblast culture medium (FCM) consisting of DMEM (BE12-604F, Lonza, Westburg, Netherlands) containing 10% FBS (10270–106, Thermo Fisher Scientific), 1% L-glutamine (BE17-605E, Lonza, Westburg, Netherlands), and 1% P/S.

    Techniques: Staining, Control, Viability Assay, Produced, Activity Assay, Fluorescence

    Journal: Frontiers in Bioengineering and Biotechnology

    Article Title: Reconstruction of the human nipple–areolar complex: a tissue engineering approach

    doi: 10.3389/fbioe.2023.1295075

    Figure Lengend Snippet:

    Article Snippet: HFs were mixed in a fibroblast culture medium (FCM) consisting of DMEM (BE12-604F, Lonza, Westburg, Netherlands) containing 10% FBS (10270–106, Thermo Fisher Scientific), 1% L-glutamine (BE17-605E, Lonza, Westburg, Netherlands), and 1% P/S.

    Techniques: Immunofluorescence, Immunohistochemistry, Immunopeptidomics, Saline, Standard Deviation