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lsm 510 meta software version 3.2  (Carl Zeiss)


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    Structured Review

    Carl Zeiss lsm 510 meta software version 3.2
    Lsm 510 Meta Software Version 3.2, supplied by Carl Zeiss, 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/lsm+510+meta+software+version+3%2E2/Software+Module+LM-EM+Correlative+Microscopy+Materials/pmc02289843-285-20-26
    Average 90 stars, based on 1 article reviews
    lsm 510 meta software version 3.2 - by Bioz Stars, 2026-10
    90/100 stars

    Images

    Related Articles

    other:

    Article Title: The Anaphase Promoting Complex Targeting Subunit Ama1 Links Meiotic Exit to Cytokinesis during Sporulation in Saccharomyces cerevisiae
    Article Snippet: To analyze fluorescence intensity, LSM 510 META software version 3.2 (Carl Zeiss) was used.

    Article Title: When the Genome Plays Dice: Circumvention of the Spindle Assembly Checkpoint and Near-Random Chromosome Segregation in Multipolar Cancer Cell Mitoses
    Article Snippet: Time-lapse images were obtained on a Zeiss LSM 510 META system with an inverted Zeiss Axiovert 100 M microscope and LSM 510 META software version 3.2 (Carl Zeiss, Jena, Germany).

    Article Title: Guinea Pig Horizontal Cells Express GABA, the GABA-Synthesizing Enzyme GAD 65 , and the GABA Vesicular Transporter
    Article Snippet: Digital confocal images were saved as Zeiss .LSM files, and final publication quality images were exported in the .TIFF format by using Zeiss LSM 510 Meta software version 3.2 (Carl Zeiss Microimaging).

    Article Title: A Thy1 -CFP DBA/2J mouse line with cyan fluorescent protein expression in retinal ganglion cells
    Article Snippet: Digital confocal stacks were saved as Zeiss .LSM files and final publication quality images were exported in the .TIFF format at 300 dpi using Zeiss LSM 510 Meta software version 3.2. images were adjusted for contrast and brightness, labeled, and formatted using Adobe Photoshop 7.0.1 (Adobe Systems, Inc., San Jose, CA) and saved at 300 dpi at their final magnification.

    Article Title: Plasmalemmal and Vesicular ?-Aminobutyric Acid Transporter Expression in the Developing Mouse Retina
    Article Snippet: Digital confocal images were saved as Zeiss LSM files, and final publication-quality images were exported in the TIFF format using Zeiss LSM 510 Meta software version 3.2 (Zeiss Ltd., Thornwood, NY).

    Article Title: Cyan fluorescent protein expression in ganglion and amacrine cells in a thy1 -CFP transgenic mouse retina
    Article Snippet: Digital confocal images were saved as Zeiss .LSM files, and final publication quality images were exported in the .TIFF format at 300 dpi using Zeiss LSM 510 Meta software version 3.2 (Zeiss Ltd., Thornwood, NY).

    Article Title: Binomial Mitotic Segregation of MYCN -Carrying Double Minutes in Neuroblastoma Illustrates the Role of Randomness in Oncogene Amplification
    Article Snippet: Cells were fixed according to Solovei et al. . Confocal images were obtained on a Zeiss LSM 510 META system with an inverted Zeiss Axiovert 100 M microscope and LSM 510 META software version 3.2 (Carl Zeiss, Jena, Germany).

    Microscopy:

    Article Title: NK cells rapidly remove B16F10 tumor cells in a perforin and interferon-gamma independent manner in vivo
    Article Snippet: Cell acquisition was performed with a dual-laser flow cytometer (FACSCalibur; BD Biosciences) and data analyzed using CellQuest version 3.3 software (BD Biosciences). .. Whole tissue pieces were placed on a microscope slide and examined for the presence and distribution of specific fluorescent cells or RFP + cells using a model LSM 510 META confocal microscope, and version 3.2 of the supporting LSM 510 META software (Carl Zeiss, Thornwood, NY, USA) that allowed single images, tile images, or image stacks to be collected. ..

    Software:

    Article Title: NK cells rapidly remove B16F10 tumor cells in a perforin and interferon-gamma independent manner in vivo
    Article Snippet: Cell acquisition was performed with a dual-laser flow cytometer (FACSCalibur; BD Biosciences) and data analyzed using CellQuest version 3.3 software (BD Biosciences). .. Whole tissue pieces were placed on a microscope slide and examined for the presence and distribution of specific fluorescent cells or RFP + cells using a model LSM 510 META confocal microscope, and version 3.2 of the supporting LSM 510 META software (Carl Zeiss, Thornwood, NY, USA) that allowed single images, tile images, or image stacks to be collected. ..



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