Discover
Features

LabGiant,

Already have an account?

In partnership with

McGill UniversityConcordia UniversityUniversité de MontréalPolytechnique MontréalDobson Centre for EntrepreneurshipUniversity of Alberta
© 2026 LabGiant
Privacy PolicyTerms of Service
    Animal Perfusion for Electron Microscopy
    Digital AssetAvailable

    Animal Perfusion for Electron Microscopy

    Faculty of Science
    Core Facility
    McGill University

    Transcardial perfusion fixation is the gold standard for fixation as it preserves ultrastructural detail and is preferable to immersion fixation. If you must perform immersion fixation, immediate immersion in fixative is essential. If the dissection requires extra time, finish trimming or blocking the tissue in a glass dish so the tissue is (always) submerged in fixative; otherwise, the tissue will fall apart during sectioning. Most types of tissues are best fixed with 2-2.5% paraformaldehyde and 2-2.5% glutaraldehyde in a 0.1M sodium cacodylate buffer. Phosphate buffer fixatives tend to precipitate out during washing with the sodium cacodylate buffer but can be used during perfusion without a problem. The percentages of glutaraldehyde and PFA vary depending on the tissue type, area of interest, etc.

    Facility for Electron Microscopy Research

    Facility for Electron Microscopy Research

    Faculty of Science

    Research lab focused on advancing scientific knowledge and innovation.

    JO

    Joaquin Ortega

    Digital AssetAvailable

    Animal Perfusion for Electron Microscopy

    Faculty of Science
    Core Facility
    McGill University

    Transcardial perfusion fixation is the gold standard for fixation as it preserves ultrastructural detail and is preferable to immersion fixation. If you must perform immersion fixation, immediate immersion in fixative is essential. If the dissection requires extra time, finish trimming or blocking the tissue in a glass dish so the tissue is (always) submerged in fixative; otherwise, the tissue will fall apart during sectioning. Most types of tissues are best fixed with 2-2.5% paraformaldehyde and 2-2.5% glutaraldehyde in a 0.1M sodium cacodylate buffer. Phosphate buffer fixatives tend to precipitate out during washing with the sodium cacodylate buffer but can be used during perfusion without a problem. The percentages of glutaraldehyde and PFA vary depending on the tissue type, area of interest, etc.

    Animal Perfusion for Electron Microscopy
    Facility for Electron Microscopy Research

    Facility for Electron Microscopy Research

    Faculty of Science

    Research lab focused on advancing scientific knowledge and innovation.

    JO

    Joaquin Ortega

    You might also like

    Discover more resources that could support your research

    Explore shared research infrastructure

    Microscopy in MontrealResearch infrastructure in MontrealCore facilities at McGill University

    In partnership with

    McGill UniversityConcordia UniversityUniversité de MontréalPolytechnique MontréalDobson Centre for EntrepreneurshipUniversity of Alberta
    © 2026 LabGiant
    Privacy PolicyTerms of Service