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blue fluorescent dna stain dapi  (Thermo Fisher)


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    Thermo Fisher blue fluorescent dna stain dapi
    Blue Fluorescent Dna Stain Dapi, supplied by Thermo Fisher, 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/result/blue fluorescent dna stain dapi/product/Thermo Fisher
    Average 99 stars, based on 1 article reviews
    blue fluorescent dna stain dapi - by Bioz Stars, 2026-06
    99/100 stars

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    Millipore blue-fluorescent dna stain 4',6-diamidino-2-phenylindole (dapi) solution
    Arl4A induces the localization of Robo1 at the plasma membrane. (A) HeLa cells were transfected with Arl4A-WT (red) or Robo-myc-WT (green) alone. (B) HeLa cells were cotransfected with Arl4A-WT and Robo1-Myc-WT. CD44 staining was used to define the plasma membrane boundary of HeLa cells. Cell nuclei were stained with <t>DAPI.</t> (C) PM/C ratios for Robo-myc-WT in the single-expression and Arl4A coexpression groups. (D) Cellular localization of Arl4A-binding defective mutants (A1 and A2) in the single-expression and Arl4A coexpression groups. (E) Quantitative data from A, B, and D. Scale bar = 10 µm. The numbers of analyzed cells are shown in each column. The solid bars represent the mean ± SD. **, P < 0.005; ***, P < 0.001 (C: Student's t test; E: one-way ANOVA with Dunnett's post hoc multiple comparison test).
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    Image Search Results


    Journal: eLife

    Article Title: Differential accumulation of storage bodies with aging defines discrete subsets of microglia in the healthy brain

    doi: 10.7554/eLife.57495

    Figure Lengend Snippet:

    Article Snippet: Other , DAPI , ThermoFisher , Cat# 62248 , Cell impermeant blue-fluorescent DNA stain for viability used at a concentration of 0.1 μg/mL.

    Techniques: Isolation, Staining, Concentration Assay, Labeling, Software, Gradient Centrifugation, Sequencing, Control, Multiplex Assay, Recombinant, Mass Spectrometry, Modification

    Arl4A induces the localization of Robo1 at the plasma membrane. (A) HeLa cells were transfected with Arl4A-WT (red) or Robo-myc-WT (green) alone. (B) HeLa cells were cotransfected with Arl4A-WT and Robo1-Myc-WT. CD44 staining was used to define the plasma membrane boundary of HeLa cells. Cell nuclei were stained with DAPI. (C) PM/C ratios for Robo-myc-WT in the single-expression and Arl4A coexpression groups. (D) Cellular localization of Arl4A-binding defective mutants (A1 and A2) in the single-expression and Arl4A coexpression groups. (E) Quantitative data from A, B, and D. Scale bar = 10 µm. The numbers of analyzed cells are shown in each column. The solid bars represent the mean ± SD. **, P < 0.005; ***, P < 0.001 (C: Student's t test; E: one-way ANOVA with Dunnett's post hoc multiple comparison test).

    Journal: Molecular Biology of the Cell

    Article Title: ADP-ribosylation factor–like 4A interacts with Robo1 to promote cell migration by regulating Cdc42 activation

    doi: 10.1091/mbc.E18-01-0001

    Figure Lengend Snippet: Arl4A induces the localization of Robo1 at the plasma membrane. (A) HeLa cells were transfected with Arl4A-WT (red) or Robo-myc-WT (green) alone. (B) HeLa cells were cotransfected with Arl4A-WT and Robo1-Myc-WT. CD44 staining was used to define the plasma membrane boundary of HeLa cells. Cell nuclei were stained with DAPI. (C) PM/C ratios for Robo-myc-WT in the single-expression and Arl4A coexpression groups. (D) Cellular localization of Arl4A-binding defective mutants (A1 and A2) in the single-expression and Arl4A coexpression groups. (E) Quantitative data from A, B, and D. Scale bar = 10 µm. The numbers of analyzed cells are shown in each column. The solid bars represent the mean ± SD. **, P < 0.005; ***, P < 0.001 (C: Student's t test; E: one-way ANOVA with Dunnett's post hoc multiple comparison test).

    Article Snippet: A blue-fluorescent DNA stain 4′,6-diamidino-2- phenylindole (DAPI) solution was purchased from Millipore (1:5000, catalogue no. S7113).

    Techniques: Clinical Proteomics, Membrane, Transfection, Staining, Expressing, Binding Assay, Comparison