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live dead double fluorescence staining  (Servicebio Inc)

 
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    Servicebio Inc live dead double fluorescence staining
    Material characterization and biocompatibility assessment of GDY-Ivy Fiber Scaffold. (A) SEM characterization: Surface morphology and local magnification of PR, PO, and POGDY scaffolds. (B) SEM image of GDY. (C) SEM-EDS elemental mapping: Distribution of C and O elements and corresponding energy spectrum analysis of the conductive scaffolds for PR, PO, and POGDY groups. (D) FTIR spectra of PO, GDY, and POGDY samples. (E) XPS spectra: High-resolution C 1s spectra of PO, GDY, and POGDY samples. (F) Data analysis of water contact angles for PR, PO, and POGDY fiber membranes, n = 5, one-way ANOVA. (G) Contact angle images of the samples, GDY0.5 specifically labeled as POGDY. <t>(H)</t> <t>Live/dead</t> cell staining of neural stem cells on the fiber conductive scaffolds from each group. (I) Quantitative analysis of cell viability for each group, n = 5. (J) CCK-8 assay: Cell viability trend at 1, 3, and 5 days of culture in different groups, two-way ANOVA. ns, not significant, ∗P < 0.05, ∗∗P < 0.01, ∗∗∗P < 0.001, n = 5.
    Live Dead Double Fluorescence Staining, supplied by Servicebio Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/live+dead+double+fluorescence+staining/pmc13022690-245-4-8?v=Servicebio+Inc
    Average 86 stars, based on 1 article reviews
    live dead double fluorescence staining - by Bioz Stars, 2026-08
    86/100 stars

    Images

    1) Product Images from "Graphdiyne-Ivy fiber neural scaffold promotes stem cell directed differentiation and neuronal maturation"

    Article Title: Graphdiyne-Ivy fiber neural scaffold promotes stem cell directed differentiation and neuronal maturation

    Journal: Materials Today Bio

    doi: 10.1016/j.mtbio.2026.103022

    Material characterization and biocompatibility assessment of GDY-Ivy Fiber Scaffold. (A) SEM characterization: Surface morphology and local magnification of PR, PO, and POGDY scaffolds. (B) SEM image of GDY. (C) SEM-EDS elemental mapping: Distribution of C and O elements and corresponding energy spectrum analysis of the conductive scaffolds for PR, PO, and POGDY groups. (D) FTIR spectra of PO, GDY, and POGDY samples. (E) XPS spectra: High-resolution C 1s spectra of PO, GDY, and POGDY samples. (F) Data analysis of water contact angles for PR, PO, and POGDY fiber membranes, n = 5, one-way ANOVA. (G) Contact angle images of the samples, GDY0.5 specifically labeled as POGDY. (H) Live/dead cell staining of neural stem cells on the fiber conductive scaffolds from each group. (I) Quantitative analysis of cell viability for each group, n = 5. (J) CCK-8 assay: Cell viability trend at 1, 3, and 5 days of culture in different groups, two-way ANOVA. ns, not significant, ∗P < 0.05, ∗∗P < 0.01, ∗∗∗P < 0.001, n = 5.
    Figure Legend Snippet: Material characterization and biocompatibility assessment of GDY-Ivy Fiber Scaffold. (A) SEM characterization: Surface morphology and local magnification of PR, PO, and POGDY scaffolds. (B) SEM image of GDY. (C) SEM-EDS elemental mapping: Distribution of C and O elements and corresponding energy spectrum analysis of the conductive scaffolds for PR, PO, and POGDY groups. (D) FTIR spectra of PO, GDY, and POGDY samples. (E) XPS spectra: High-resolution C 1s spectra of PO, GDY, and POGDY samples. (F) Data analysis of water contact angles for PR, PO, and POGDY fiber membranes, n = 5, one-way ANOVA. (G) Contact angle images of the samples, GDY0.5 specifically labeled as POGDY. (H) Live/dead cell staining of neural stem cells on the fiber conductive scaffolds from each group. (I) Quantitative analysis of cell viability for each group, n = 5. (J) CCK-8 assay: Cell viability trend at 1, 3, and 5 days of culture in different groups, two-way ANOVA. ns, not significant, ∗P < 0.05, ∗∗P < 0.01, ∗∗∗P < 0.001, n = 5.

    Techniques Used: Labeling, Staining, CCK-8 Assay



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    Image Search Results


    Material characterization and biocompatibility assessment of GDY-Ivy Fiber Scaffold. (A) SEM characterization: Surface morphology and local magnification of PR, PO, and POGDY scaffolds. (B) SEM image of GDY. (C) SEM-EDS elemental mapping: Distribution of C and O elements and corresponding energy spectrum analysis of the conductive scaffolds for PR, PO, and POGDY groups. (D) FTIR spectra of PO, GDY, and POGDY samples. (E) XPS spectra: High-resolution C 1s spectra of PO, GDY, and POGDY samples. (F) Data analysis of water contact angles for PR, PO, and POGDY fiber membranes, n = 5, one-way ANOVA. (G) Contact angle images of the samples, GDY0.5 specifically labeled as POGDY. (H) Live/dead cell staining of neural stem cells on the fiber conductive scaffolds from each group. (I) Quantitative analysis of cell viability for each group, n = 5. (J) CCK-8 assay: Cell viability trend at 1, 3, and 5 days of culture in different groups, two-way ANOVA. ns, not significant, ∗P < 0.05, ∗∗P < 0.01, ∗∗∗P < 0.001, n = 5.

    Journal: Materials Today Bio

    Article Title: Graphdiyne-Ivy fiber neural scaffold promotes stem cell directed differentiation and neuronal maturation

    doi: 10.1016/j.mtbio.2026.103022

    Figure Lengend Snippet: Material characterization and biocompatibility assessment of GDY-Ivy Fiber Scaffold. (A) SEM characterization: Surface morphology and local magnification of PR, PO, and POGDY scaffolds. (B) SEM image of GDY. (C) SEM-EDS elemental mapping: Distribution of C and O elements and corresponding energy spectrum analysis of the conductive scaffolds for PR, PO, and POGDY groups. (D) FTIR spectra of PO, GDY, and POGDY samples. (E) XPS spectra: High-resolution C 1s spectra of PO, GDY, and POGDY samples. (F) Data analysis of water contact angles for PR, PO, and POGDY fiber membranes, n = 5, one-way ANOVA. (G) Contact angle images of the samples, GDY0.5 specifically labeled as POGDY. (H) Live/dead cell staining of neural stem cells on the fiber conductive scaffolds from each group. (I) Quantitative analysis of cell viability for each group, n = 5. (J) CCK-8 assay: Cell viability trend at 1, 3, and 5 days of culture in different groups, two-way ANOVA. ns, not significant, ∗P < 0.05, ∗∗P < 0.01, ∗∗∗P < 0.001, n = 5.

    Article Snippet: Cytotoxicity was assessed via Live/Dead double fluorescence staining (Servicebio, China), with live cells stained green and dead cells stained red.

    Techniques: Labeling, Staining, CCK-8 Assay