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pco.edge 4.2  (Excelitas corp)


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    Excelitas corp pco.edge 4.2
    Pco.Edge 4.2, supplied by Excelitas corp, used in various techniques. Bioz Stars score: 99/100, based on 5069 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/xcite/excelitas+corp___pco_edge_group?v=Excelitas+corp
    Average 99 stars, based on 5069 article reviews
    pco.edge 4.2 - by Bioz Stars, 2026-07
    99/100 stars

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    Image Search Results


    Clearance of conidia of N. crassa wtA from the nodules of Galleria mellonella larvae, 3 h, 24 h, and 48 h post-injection. Conidia (indicated by arrow) were present in small numbers in nodules extracted 24 h post-injection. Calcofluor white stained nodules were visualized by 400× magnification (excitation/emission 350/461 nm).

    Journal: The Cell Surface

    Article Title: Neurospora crassa Δ ccg-8 compromises cell surface integrity and antifungal tolerance: Insights from in vitro and Galleria mellonella studies

    doi: 10.1016/j.tcsw.2026.100172

    Figure Lengend Snippet: Clearance of conidia of N. crassa wtA from the nodules of Galleria mellonella larvae, 3 h, 24 h, and 48 h post-injection. Conidia (indicated by arrow) were present in small numbers in nodules extracted 24 h post-injection. Calcofluor white stained nodules were visualized by 400× magnification (excitation/emission 350/461 nm).

    Article Snippet: Nodules were immediately examined using a microscope Axio Imager A1 (Zeiss, Germany) – 400 × magnification, fluorescence detected using excitation/emission wavelength 365/440 nm (X-Cite 120Q lamp, Excelitas Technologies, USA) with photo documentation equipment Axiocam ICC 1 and AxioVision 4.8 software.

    Techniques: Injection, Staining

    Clearance of conidia of N. crassa Δ ccg-8 from the nodules of Galleria mellonella larvae, 3 h, 24 h, and 48 h post-injection. Conidia (indicated by arrow) were last present in nodules extracted 3 h post-injection. Calcofluor white stained nodules were visualized by 400× magnification (excitation/emission 350/461 nm).

    Journal: The Cell Surface

    Article Title: Neurospora crassa Δ ccg-8 compromises cell surface integrity and antifungal tolerance: Insights from in vitro and Galleria mellonella studies

    doi: 10.1016/j.tcsw.2026.100172

    Figure Lengend Snippet: Clearance of conidia of N. crassa Δ ccg-8 from the nodules of Galleria mellonella larvae, 3 h, 24 h, and 48 h post-injection. Conidia (indicated by arrow) were last present in nodules extracted 3 h post-injection. Calcofluor white stained nodules were visualized by 400× magnification (excitation/emission 350/461 nm).

    Article Snippet: Nodules were immediately examined using a microscope Axio Imager A1 (Zeiss, Germany) – 400 × magnification, fluorescence detected using excitation/emission wavelength 365/440 nm (X-Cite 120Q lamp, Excelitas Technologies, USA) with photo documentation equipment Axiocam ICC 1 and AxioVision 4.8 software.

    Techniques: Injection, Staining

    The infection process by conidia of A. fumigatus CCF6600 in the Galleria mellonella larvae, 3 h, 24 h, and 48 h post-injection. Conidia (indicated by arrow) survived the effect of the innate immune system of larvae in nodules, and after 48 h post-infection, they germinated. Calcofluor white stained nodules were visualized by 400× magnification (excitation/emission 350/461 nm).

    Journal: The Cell Surface

    Article Title: Neurospora crassa Δ ccg-8 compromises cell surface integrity and antifungal tolerance: Insights from in vitro and Galleria mellonella studies

    doi: 10.1016/j.tcsw.2026.100172

    Figure Lengend Snippet: The infection process by conidia of A. fumigatus CCF6600 in the Galleria mellonella larvae, 3 h, 24 h, and 48 h post-injection. Conidia (indicated by arrow) survived the effect of the innate immune system of larvae in nodules, and after 48 h post-infection, they germinated. Calcofluor white stained nodules were visualized by 400× magnification (excitation/emission 350/461 nm).

    Article Snippet: Nodules were immediately examined using a microscope Axio Imager A1 (Zeiss, Germany) – 400 × magnification, fluorescence detected using excitation/emission wavelength 365/440 nm (X-Cite 120Q lamp, Excelitas Technologies, USA) with photo documentation equipment Axiocam ICC 1 and AxioVision 4.8 software.

    Techniques: Infection, Injection, Staining