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Methodenartikel

Frozen Mouse Brain Tissue Sectioning: A Procedure to Obtain Thin Frozen Tissue Sections from Frozen Murine Brain Tissue

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30 april 2023

In dit artikel

Samenvatting

Source: Comba, A. et al. Laser Capture Microdissection of Glioma Subregions for Spatial and Molecular Characterization of Intratumoral Heterogeneity, Oncostreams, and Invasion. J. Vis. Exp. (2020)

In this video, we demonstrate the sectioning of a frozen mouse brain tumor tissue using a cryostat. The frozen brain tissue sections so obtained are stored at low temperatures until further analysis.

Protocol

All procedures involving animal models have been reviewed by the local institutional animal care committee and the JoVE veterinary review board.

1. Sectioning Frozen Brain Tumor Tissues

  1. Label 2 µm polyethylene naphthalate (PEN) slides with the sample information. Tissue sections will be placed directly on these slides following sectioning.
  2. Set the temperature of the cryostat chamber between -20 to -24 °C. Before sectioning, place the sample block in the cryostat chamber and let it equilibrate to the temperature in the chamber for 30–60 min.
  3. Clean the cryostat chamber and the k....

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Openbaarmakingen

No conflicts of interest declared.

Materialen

Lijst van materialen gebruikt in dit artikel
NaamBedrijfCatalogusnummerOpmerkingen
PEN Membrane Glass Slide (2 µm)Lieca1150518
Research CryostatLeicaCM3050s
RNaseZap RNase Decontamination SolutionFisher ScientificAM9780
Peel Away Disposable Embedding MoldsElectron Microscopy Sciences70182
Pinpoint SolutionZymo ResearchD3001-1
Tissue-Plus O.C.T. CompoundFisher Scientific23-730-571

Tags

Cryostaat-weefselcoupesbevroren hersenweefselmontage van weefselcoupespositief geladen glasplaatjesopslag bij lage temperatuurtemperatuurequilibratie van de cryostaatuitlijning van het weefselblokRNase-vrije hanteringcoupes van hersentumorweefsel