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cellsurgeon multiphoton microscope  (Rowiak GmbH)

 
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    Structured Review

    Rowiak GmbH cellsurgeon multiphoton microscope
    Mean DNA (A) , sGAG (B) , HYP (C) and dHYP (D) content per dry weight of native PTA and decellularized PTA scaffolds treated with (M2) or without (M1) RNase/DNase and sterilized with either PAA or γ-irradiation. Data was expressed as means ( n = 6); error bars indicate 95% C.I.; MSD: minimum significant difference; indicates significant difference between the native and the decellularized groups. Connectors indicate significant difference between the originator and end arrow group. (E–G) Characteristic en face <t>multiphoton</t> images of the lumen of decellularized PTAs, treated with M1 and sterilized with either PAA (E,F) or γ-irradiation (G) , showing the elastic fiber network of internal elastic lamina (E, G; imaging plane was approximately 20 μm below lumen surface) and the collagen fibers of tunica media (F; imaging plane was about 60 μm below lumen surface). Black arrow heads (►) show elastic fibers. Scale bars indicate 100 μm (E,F) or 50 μm (G) .
    Cellsurgeon Multiphoton Microscope, supplied by Rowiak GmbH, 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/cellsurgeon+multiphoton+microscope/cellsurgeon+multiphoton+microscope/pmc09889865-73-7-11
    Average 90 stars, based on 1 article reviews
    cellsurgeon multiphoton microscope - by Bioz Stars, 2026-11
    90/100 stars

    Images

    1) Product Images from "Development of a dual-component infection-resistant arterial replacement for small-caliber reconstructions: A proof-of-concept study"

    Article Title: Development of a dual-component infection-resistant arterial replacement for small-caliber reconstructions: A proof-of-concept study

    Journal: Frontiers in Bioengineering and Biotechnology

    doi: 10.3389/fbioe.2023.957458

    Mean DNA (A) , sGAG (B) , HYP (C) and dHYP (D) content per dry weight of native PTA and decellularized PTA scaffolds treated with (M2) or without (M1) RNase/DNase and sterilized with either PAA or γ-irradiation. Data was expressed as means ( n = 6); error bars indicate 95% C.I.; MSD: minimum significant difference; indicates significant difference between the native and the decellularized groups. Connectors indicate significant difference between the originator and end arrow group. (E–G) Characteristic en face multiphoton images of the lumen of decellularized PTAs, treated with M1 and sterilized with either PAA (E,F) or γ-irradiation (G) , showing the elastic fiber network of internal elastic lamina (E, G; imaging plane was approximately 20 μm below lumen surface) and the collagen fibers of tunica media (F; imaging plane was about 60 μm below lumen surface). Black arrow heads (►) show elastic fibers. Scale bars indicate 100 μm (E,F) or 50 μm (G) .
    Figure Legend Snippet: Mean DNA (A) , sGAG (B) , HYP (C) and dHYP (D) content per dry weight of native PTA and decellularized PTA scaffolds treated with (M2) or without (M1) RNase/DNase and sterilized with either PAA or γ-irradiation. Data was expressed as means ( n = 6); error bars indicate 95% C.I.; MSD: minimum significant difference; indicates significant difference between the native and the decellularized groups. Connectors indicate significant difference between the originator and end arrow group. (E–G) Characteristic en face multiphoton images of the lumen of decellularized PTAs, treated with M1 and sterilized with either PAA (E,F) or γ-irradiation (G) , showing the elastic fiber network of internal elastic lamina (E, G; imaging plane was approximately 20 μm below lumen surface) and the collagen fibers of tunica media (F; imaging plane was about 60 μm below lumen surface). Black arrow heads (►) show elastic fibers. Scale bars indicate 100 μm (E,F) or 50 μm (G) .

    Techniques Used: Irradiation, Imaging

    Related Articles

    Imaging:

    Article Title: Development of a dual-component infection-resistant arterial replacement for small-caliber reconstructions: A proof-of-concept study
    Article Snippet: .. The multiphoton imaging was performed using a CellSurgeon multiphoton microscope (MPM; LLS-ROWIAK). .. The MPM comprised a femtosecond mode-locked near infrared 705–980 nm Ti:Sapphire laser (Chameleon XR, Coherent) and a microscope.

    Microscopy:

    Article Title: Development of a dual-component infection-resistant arterial replacement for small-caliber reconstructions: A proof-of-concept study
    Article Snippet: .. The multiphoton imaging was performed using a CellSurgeon multiphoton microscope (MPM; LLS-ROWIAK). .. The MPM comprised a femtosecond mode-locked near infrared 705–980 nm Ti:Sapphire laser (Chameleon XR, Coherent) and a microscope.



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    cellsurgeon multiphoton microscope  (Rowiak GmbH)
    90
    Rowiak GmbH cellsurgeon multiphoton microscope
    Mean DNA (A) , sGAG (B) , HYP (C) and dHYP (D) content per dry weight of native PTA and decellularized PTA scaffolds treated with (M2) or without (M1) RNase/DNase and sterilized with either PAA or γ-irradiation. Data was expressed as means ( n = 6); error bars indicate 95% C.I.; MSD: minimum significant difference; indicates significant difference between the native and the decellularized groups. Connectors indicate significant difference between the originator and end arrow group. (E–G) Characteristic en face <t>multiphoton</t> images of the lumen of decellularized PTAs, treated with M1 and sterilized with either PAA (E,F) or γ-irradiation (G) , showing the elastic fiber network of internal elastic lamina (E, G; imaging plane was approximately 20 μm below lumen surface) and the collagen fibers of tunica media (F; imaging plane was about 60 μm below lumen surface). Black arrow heads (►) show elastic fibers. Scale bars indicate 100 μm (E,F) or 50 μm (G) .
    Cellsurgeon Multiphoton Microscope, supplied by Rowiak GmbH, 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/cellsurgeon+multiphoton+microscope/cellsurgeon+multiphoton+microscope/pmc09889865-73-7-11
    Average 90 stars, based on 1 article reviews
    cellsurgeon multiphoton microscope - by Bioz Stars, 2026-11
    90/100 stars
    		  Buy from Supplier

    Image Search Results


    Mean DNA (A) , sGAG (B) , HYP (C) and dHYP (D) content per dry weight of native PTA and decellularized PTA scaffolds treated with (M2) or without (M1) RNase/DNase and sterilized with either PAA or γ-irradiation. Data was expressed as means ( n = 6); error bars indicate 95% C.I.; MSD: minimum significant difference; indicates significant difference between the native and the decellularized groups. Connectors indicate significant difference between the originator and end arrow group. (E–G) Characteristic en face multiphoton images of the lumen of decellularized PTAs, treated with M1 and sterilized with either PAA (E,F) or γ-irradiation (G) , showing the elastic fiber network of internal elastic lamina (E, G; imaging plane was approximately 20 μm below lumen surface) and the collagen fibers of tunica media (F; imaging plane was about 60 μm below lumen surface). Black arrow heads (►) show elastic fibers. Scale bars indicate 100 μm (E,F) or 50 μm (G) .

    Journal: Frontiers in Bioengineering and Biotechnology

    Article Title: Development of a dual-component infection-resistant arterial replacement for small-caliber reconstructions: A proof-of-concept study

    doi: 10.3389/fbioe.2023.957458

    Figure Lengend Snippet: Mean DNA (A) , sGAG (B) , HYP (C) and dHYP (D) content per dry weight of native PTA and decellularized PTA scaffolds treated with (M2) or without (M1) RNase/DNase and sterilized with either PAA or γ-irradiation. Data was expressed as means ( n = 6); error bars indicate 95% C.I.; MSD: minimum significant difference; indicates significant difference between the native and the decellularized groups. Connectors indicate significant difference between the originator and end arrow group. (E–G) Characteristic en face multiphoton images of the lumen of decellularized PTAs, treated with M1 and sterilized with either PAA (E,F) or γ-irradiation (G) , showing the elastic fiber network of internal elastic lamina (E, G; imaging plane was approximately 20 μm below lumen surface) and the collagen fibers of tunica media (F; imaging plane was about 60 μm below lumen surface). Black arrow heads (►) show elastic fibers. Scale bars indicate 100 μm (E,F) or 50 μm (G) .

    Article Snippet: The multiphoton imaging was performed using a CellSurgeon multiphoton microscope (MPM; LLS-ROWIAK).

    Techniques: Irradiation, Imaging