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ocelloscope imager  (BioSense Solutions ApS)


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    BioSense Solutions ApS ocelloscope imager
    Ocelloscope Imager, supplied by BioSense Solutions ApS, used in various techniques. Bioz Stars score: 95/100, based on 60 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/ocelloscope+imager/oCelloScope/pm42000315-59-16-18
    Average 95 stars, based on 60 article reviews
    ocelloscope imager - by Bioz Stars, 2026-09
    95/100 stars

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    Related Articles

    Software:

    Article Title: Cellular dynamics in liquid static cultures of Aureobasidiumpullulans.
    Article Snippet: To perform timelapse microscopy of liquid static cultures, wells of 24 wells suspension culture plates (Greiner Bio-one, Cellstar 662160, www. gbo.com) were filled with 400 μl potato dextrose broth (PDB), pH 5 (BD Difco, Lawrence, USA), and inoculated with 103 A. pullulans cells. .. Growth and differentiation of A. pullulans were monitored under static conditions at 26 ◦C using an oCelloScope imager (Biosense Solutions, www.biosensesolutions.dk) (Fredborg et al., 2013) with UniExplorer software version 8.1.0.7682-RL2 using biological triplicates (i.e. three independent experiments with different inoculum and medium stocks), each with three technical replicates (i.e. three wells inoculated with the same inoculum and medium stocks). ..

    Article Title: Minimal nutrient requirements for induction of germination of Aspergillus niger conidia.
    Article Snippet: .. 135 Germination of conidia was monitored on line at 30 °C using an oCelloScope imager 136 (Biosense Solutions, www.biosensesolutions.dk) (Fredborg et al., 2013) with 137 UniExplorer software version 8.1.0.7682-RL2. ..



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    Four isolates of each species were used and grown on three locust-derived media (A – C) and the ¼ SDAY control medium (D). Medium A represents the twice filtered locust medium, Medium B represents the once filtered locust medium, and Medium C represents the unfiltered locust medium. Over the course of 7 days, radial growth and sporulation were monitored using a Reshape imaging robot. Thereafter, conidia were harvested to measure spore count, germination rate, and maximum growth in ¼ SDY medium using an oCelloscope TM imaging system. Lastly, pathogenicity assays were conducted using selected M. brunneum isolates on using Tenebrio molitor larvae.

    Journal: bioRxiv

    Article Title: Improving the production and virulence of entomopathogenic fungi for biological control using insect-derived in vitro culture medium

    doi: 10.64898/2026.03.14.711814

    Figure Lengend Snippet: Four isolates of each species were used and grown on three locust-derived media (A – C) and the ¼ SDAY control medium (D). Medium A represents the twice filtered locust medium, Medium B represents the once filtered locust medium, and Medium C represents the unfiltered locust medium. Over the course of 7 days, radial growth and sporulation were monitored using a Reshape imaging robot. Thereafter, conidia were harvested to measure spore count, germination rate, and maximum growth in ¼ SDY medium using an oCelloscope TM imaging system. Lastly, pathogenicity assays were conducted using selected M. brunneum isolates on using Tenebrio molitor larvae.

    Article Snippet: Each isolate x medium of origin combination was plated in triplicate and the oCelloScope Imaging system (BioSense Solutions, Denmark) was used to track the germination and growth of the isolates over the course of 48 hours.

    Techniques: Derivative Assay, Control, Imaging