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escherichia coli dh5α  (ATCC)


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    Structured Review

    ATCC escherichia coli dh5α
    Comparison of itaconic acid-producing strains (Kuenz et al. <xref ref-type=2012 ; Harder et al. 2018 ) " width="250" height="auto" />
    Escherichia Coli Dh5α, supplied by ATCC, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/insert/pmc10771365-74-0-3?v=ATCC
    Average 92 stars, based on 1 article reviews
    escherichia coli dh5α - by Bioz Stars, 2026-08
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    Images

    1) Product Images from "Metabolic engineering of Shewanella oneidensis to produce glutamate and itaconic acid"

    Article Title: Metabolic engineering of Shewanella oneidensis to produce glutamate and itaconic acid

    Journal: Applied Microbiology and Biotechnology

    doi: 10.1007/s00253-023-12879-5

    2012 ; Harder et al. 2018 ) " title="Comparison of itaconic acid-producing strains (Kuenz et al. 2012 ; Harder" property="contentUrl" width="100%" height="100%"/>
    Figure Legend Snippet: Comparison of itaconic acid-producing strains (Kuenz et al. 2012 ; Harder et al. 2018 )

    Techniques Used: Comparison



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    Image Search Results


    Evaluation of angiogenic potential induced by Mg 2+ and NRP-1. ( A ) Scratch assay in three different microenvironments. ( B ) Transwell assay in three different microenvironments. ( C ) Quantitative analysis of wound healing area. ( D ) Quantitative analysis of number of migration cells. ( E ) Immunofluorescence staining of VEGFA and FGF2, with DAPI for nuclear staining and F-actin for cytoskeleton labeling. ( F ) Tube formation evaluation in four different microenvironments. ( G ) Quantitative analysis of number of junction. ( H ) Quantitative analysis of Flu intensity. ( I ) Western-blot analysis of VEGFA, FGF2, and Nr4a1. ( J-L ) Quantitative analysis of relative protein expression of VEGFA, FGF2, and Nr4a1. Data are presented as mean values ± s.d. (n = 3). ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001 (one-way ANOVA).

    Journal: Bioactive Materials

    Article Title: Reconstructing the ischemic osteogenic microenvironment through hierarchical scaffolds orchestrating Mg 2+ signaling and neuropilin-1–mediated angiogenesis

    doi: 10.1016/j.bioactmat.2026.02.031

    Figure Lengend Snippet: Evaluation of angiogenic potential induced by Mg 2+ and NRP-1. ( A ) Scratch assay in three different microenvironments. ( B ) Transwell assay in three different microenvironments. ( C ) Quantitative analysis of wound healing area. ( D ) Quantitative analysis of number of migration cells. ( E ) Immunofluorescence staining of VEGFA and FGF2, with DAPI for nuclear staining and F-actin for cytoskeleton labeling. ( F ) Tube formation evaluation in four different microenvironments. ( G ) Quantitative analysis of number of junction. ( H ) Quantitative analysis of Flu intensity. ( I ) Western-blot analysis of VEGFA, FGF2, and Nr4a1. ( J-L ) Quantitative analysis of relative protein expression of VEGFA, FGF2, and Nr4a1. Data are presented as mean values ± s.d. (n = 3). ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001 (one-way ANOVA).

    Article Snippet: For the Transwell assay, BMSCs were seeded in the upper chambers of Transwell inserts (8.0 μm pore size; Servicebio, China), while different culture conditions were applied in the lower chambers according to the experimental groups.

    Techniques: Wound Healing Assay, Transwell Assay, Migration, Immunofluorescence, Staining, Labeling, Western Blot, Expressing