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axiovision 4 module 3d deconvolution  (Carl Zeiss)


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    Carl Zeiss axiovision 4 module 3d deconvolution
    Axiovision 4 Module 3d Deconvolution, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/axiovision+3d+deconvolution+module/AxioVision+4+Module+Z-Stack/pmc03290648-146-41-46
    Average 91 stars, based on 1 article reviews
    axiovision 4 module 3d deconvolution - by Bioz Stars, 2026-09
    91/100 stars

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    Related Articles

    Software:

    Article Title: Distribution and spatiotemporal development of organised lymphoid tissues in the chicken intestinal tract.
    Article Snippet: .. Images were analysed by ZEN software (Carl Zeiss Zen pro2012 software). ..

    Article Title: Establishment of a glucocorticoid inducible system for regulating somatic embryogenesis in Liriodendron hybrids
    Article Snippet: .. The fluorescence intensity was measured using the irregular measurement tool within Zeiss Zen software (Carl Zeiss, Germany), which allowed us to select regions of interest displaying GFP fluorescence within the nucleus. ..

    Article Title: Activity of Synthetic Peptide KP and Its Derivatives against Biofilm-Producing Escherichia coli Strains Resistant to Cephalosporins.
    Article Snippet: .. CLSM images were acquired, and 3D reconstructions were generated using the Axiovision software module Inside 4D release 4.5 (Carl Zeiss, Jena, Germany). .. The ratio of red fluorescence intensity (FI) to combined green-and-red FI, calculated with Imaris 9.5.0 software (Bitplane AG, Zurich, Switzerland), was used to determine the proportion of dead cells in the treatment groups.

    Article Title: Injury-induced KIF4A neural expression and its role in Schwann cell proliferation suggest a dual function for this kinesin in neural regeneration
    Article Snippet: For fluorescence-labelled sections, nuclei were counterstained with 4′,6-diamidino-2-phenylindole (DAPI) solution (1:10, Roche Diagnostics Deutschland GmbH, Mannheim, Germany) and, after washing, were sections immersed in 70% EtOH for 5 minutes, transferred to 0.3% Sudan Black (Sigma-Aldrich), and mounted with EprediaTM ShandonTM Immu-MountTM (Thermo Fisher Scientific, Darmstadt, Germany). .. Fluorescence-labelled sections were photographed using either the fluorescence microscope Axioplan 2 with AxioVision Rel 4.8 software, or an LSM 880 Meta confocal microscope (both from Carl Zeiss, Jena, Germany). ..

    other:

    Article Title: The Assessment of a Novel Endoscopic Ultrasound-Compatible Cryocatheter to Ablate Pancreatic Cancer
    Article Snippet: The Zeiss ZEN 2.3 Pro software measurement tool was then used to measure the diameters of the necrotic zones within the TEMs.

    Fluorescence:

    Article Title: Establishment of a glucocorticoid inducible system for regulating somatic embryogenesis in Liriodendron hybrids
    Article Snippet: .. The fluorescence intensity was measured using the irregular measurement tool within Zeiss Zen software (Carl Zeiss, Germany), which allowed us to select regions of interest displaying GFP fluorescence within the nucleus. ..

    Article Title: Exploring the multifaceted impact of lanthanides on physiological pathways in human breast cancer cells.
    Article Snippet: Lanthanum (La) and cerium (Ce), rare earth elements with physical properties similar to calcium (Ca), are generally considered non-toxic when used appropriately.. However, their ions possess anti-tumor capabilities.. This investigation explores the potential applications and mechanisms of LaCl3 or CeCl3 treatment in triplenegative breast cancer (TNBC) cell lines.

    Article Title: Injury-induced KIF4A neural expression and its role in Schwann cell proliferation suggest a dual function for this kinesin in neural regeneration
    Article Snippet: For fluorescence-labelled sections, nuclei were counterstained with 4′,6-diamidino-2-phenylindole (DAPI) solution (1:10, Roche Diagnostics Deutschland GmbH, Mannheim, Germany) and, after washing, were sections immersed in 70% EtOH for 5 minutes, transferred to 0.3% Sudan Black (Sigma-Aldrich), and mounted with EprediaTM ShandonTM Immu-MountTM (Thermo Fisher Scientific, Darmstadt, Germany). .. Fluorescence-labelled sections were photographed using either the fluorescence microscope Axioplan 2 with AxioVision Rel 4.8 software, or an LSM 880 Meta confocal microscope (both from Carl Zeiss, Jena, Germany). ..

    Article Title: End binding-3 inhibitor activates regenerative program in age-related macular degeneration
    Article Snippet: Cells were loaded with Fura-2 a.m. (Life Technologies) at the same time. .. Fura-2 fluorescence was excited at 340 and 380 nm and collected at 510 ± 80 nm using an Axiovert 100 inverted microscope (Carl Zeiss) equipped with Plan-Apo 60× with the numerical aperture (NA) 1.4 oil immersion objective, Lambda DG-4 switcher illumination system (Sutter Instruments), AxioCom Hsm camera (Zeiss), fura-2 filter set (Chroma), and AxioVision Physiology Acquisition module. ..

    Confocal Laser Scanning Microscopy:

    Article Title: Activity of Synthetic Peptide KP and Its Derivatives against Biofilm-Producing Escherichia coli Strains Resistant to Cephalosporins.
    Article Snippet: .. CLSM images were acquired, and 3D reconstructions were generated using the Axiovision software module Inside 4D release 4.5 (Carl Zeiss, Jena, Germany). .. The ratio of red fluorescence intensity (FI) to combined green-and-red FI, calculated with Imaris 9.5.0 software (Bitplane AG, Zurich, Switzerland), was used to determine the proportion of dead cells in the treatment groups.

    Generated:

    Article Title: Activity of Synthetic Peptide KP and Its Derivatives against Biofilm-Producing Escherichia coli Strains Resistant to Cephalosporins.
    Article Snippet: .. CLSM images were acquired, and 3D reconstructions were generated using the Axiovision software module Inside 4D release 4.5 (Carl Zeiss, Jena, Germany). .. The ratio of red fluorescence intensity (FI) to combined green-and-red FI, calculated with Imaris 9.5.0 software (Bitplane AG, Zurich, Switzerland), was used to determine the proportion of dead cells in the treatment groups.

    Microscopy:

    Article Title: Injury-induced KIF4A neural expression and its role in Schwann cell proliferation suggest a dual function for this kinesin in neural regeneration
    Article Snippet: For fluorescence-labelled sections, nuclei were counterstained with 4′,6-diamidino-2-phenylindole (DAPI) solution (1:10, Roche Diagnostics Deutschland GmbH, Mannheim, Germany) and, after washing, were sections immersed in 70% EtOH for 5 minutes, transferred to 0.3% Sudan Black (Sigma-Aldrich), and mounted with EprediaTM ShandonTM Immu-MountTM (Thermo Fisher Scientific, Darmstadt, Germany). .. Fluorescence-labelled sections were photographed using either the fluorescence microscope Axioplan 2 with AxioVision Rel 4.8 software, or an LSM 880 Meta confocal microscope (both from Carl Zeiss, Jena, Germany). ..

    Inverted Microscopy:

    Article Title: End binding-3 inhibitor activates regenerative program in age-related macular degeneration
    Article Snippet: Cells were loaded with Fura-2 a.m. (Life Technologies) at the same time. .. Fura-2 fluorescence was excited at 340 and 380 nm and collected at 510 ± 80 nm using an Axiovert 100 inverted microscope (Carl Zeiss) equipped with Plan-Apo 60× with the numerical aperture (NA) 1.4 oil immersion objective, Lambda DG-4 switcher illumination system (Sutter Instruments), AxioCom Hsm camera (Zeiss), fura-2 filter set (Chroma), and AxioVision Physiology Acquisition module. ..



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