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ex vivo porcine explants in a prototype colonic simulator  (Endosim LLC)

 
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    Endosim LLC ex vivo porcine explants in a prototype colonic simulator
    Ex Vivo Porcine Explants In A Prototype Colonic Simulator, supplied by Endosim LLC, 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/ex+vivo+colons/ex+vivo+porcine+explants+in+a+prototype+colonic+simulator/pm28281126-44-12-15
    Average 90 stars, based on 1 article reviews
    ex vivo porcine explants in a prototype colonic simulator - by Bioz Stars, 2026-09
    90/100 stars

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    Related Articles

    Ex Vivo:

    Article Title: Learning colorectal endoscopic submucosal dissection: a prospective learning curve study using a novel ex vivo simulator.
    Article Snippet: was 14.4% and the aggregate rate of non-en bloc resection was 5.6%.. Using a composite quality score integrating complications and procedural time, it was found that there was a significant difference between two local polynomial regression lines when using a cut-point at the 9th procedure (p = 0.04), reflecting the point at which most of the learning curve is traversed.. Conclusions In this study, there were significant improvements realized in colonic ESD performance after 9 colon ESD procedures in ex vivo specimens.



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    Colonic secretion of pro- and anti-inflammatory mediators in Campylobacter infected conventional mice. Conventionally colonized C57BL/6 mice were perorally infected with C. jejuni (open circles) or C. coli (closed circles) on day (d) 0 and d1 by gavage. On day 21 post-infection, (A) IFN-γ, (B) TNF-α, (C) MCP-1, (D) IL-6, (E) IL-12p70 and (F) IL-10 concentrations were determined in supernatants derived from colonic ex vivo biopsies. Naive mice served as negative control animals (open diamonds). Medians (black bars), levels of significance (P -values) assessed by the Kruskal-Wallis test and Dunn’s post-correction and numbers of analyzed animals (in parentheses) are indicated. Data were pooled from four independent experiments

    Journal: European Journal of Microbiology & Immunology

    Article Title: The conundrum of colonization resistance against Campylobacter reloaded: The gut microbota composition in conventional mice does not prevent from Campylobacter coli infection

    doi: 10.1556/1886.2020.00004

    Figure Lengend Snippet: Colonic secretion of pro- and anti-inflammatory mediators in Campylobacter infected conventional mice. Conventionally colonized C57BL/6 mice were perorally infected with C. jejuni (open circles) or C. coli (closed circles) on day (d) 0 and d1 by gavage. On day 21 post-infection, (A) IFN-γ, (B) TNF-α, (C) MCP-1, (D) IL-6, (E) IL-12p70 and (F) IL-10 concentrations were determined in supernatants derived from colonic ex vivo biopsies. Naive mice served as negative control animals (open diamonds). Medians (black bars), levels of significance (P -values) assessed by the Kruskal-Wallis test and Dunn’s post-correction and numbers of analyzed animals (in parentheses) are indicated. Data were pooled from four independent experiments

    Article Snippet: Colonic ex vivo biopsies were cut longitudinally, washed in phosphate buffered saline (PBS; Gibco, Life Technologies, UK), and strips of approximately 1 cm 2 tissue and ex vivo biopsies derived from the spleen (one half) were placed in 24-flat-bottom well culture plates (Nunc, Germany) containing 500 μL serum-free RPMI 1640 medium (Gibco, life technologies, UK) supplemented with penicillin (100 U/mL) and streptomycin (100 μg/mL; PAA Laboratories, Germany).

    Techniques: Infection, Derivative Assay, Ex Vivo, Negative Control