Rodent Tissue Isolation

Rodent tissue isolation is the laboratory process of separating organs, tissues, or cellular regions from a rodent for controlled biological analysis. It typically involves humane tissue collection followed by dissection, removal of unwanted material, and mechanical or enzymatic separation under sterile, temperature-controlled conditions to preserve tissue structure and viability. Isolated samples support studies of anatomy, physiology, cell biology, disease mechanisms, drug responses, and tissue-specific gene or protein expression. Careful handling, consistent sampling, and appropriate preservation improve reproducibility and help researchers connect cellular findings with organ-level function in experimental biology.

Rodent Tissue Isolation - Related Videos

Research

JoVE Journal - Biochemistry

Robust Mitochondrial Isolation from Rodent Cardiac Tissue

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Cited by 1 •

2024

Bioenergetic and metabolomic studies on mitochondria have revealed their multifaceted role in many diseases, but the isolation methods for these organelles vary. The method detailed here is capable of purifying high-quality mitochondria from multiple tissue sources. Quality is determined by respiratory control ratios and other metrics assessed with high-resolution respirometry.

Research

JoVE Journal - Neuroscience
Free Sample

Isolating Nasal Olfactory Stem Cells from Rodents or Humans

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Cited by 98 •

2011

We describe here a method for biopsying olfactory mucosa from rat and human nasal cavities. These biopsies can be used for either identifying molecular anomalies in brain diseases or isolating multipotent adult stem cells that can be utilized for cell transplantation in animal models of brain trauma/disease.

Research

JoVE Journal - Neuroscience
Free Sample

Hydraulic Extrusion of the Spinal Cord and Isolation of Dorsal Root Ganglia in Rodents

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Cited by 110 •

2017

Here, we present a protocol for hydraulic extrusion of the spinal cord as well as identification and isolation of specific dorsal root ganglia (DRGs) in the same rodent. Compared to standard spinal cord isolation methods, this method is significantly faster and reduces the risk of tissue damage.

Research

JoVE Journal - Biochemistry
Free Sample

Shotgun Lipidomics of Rodent Tissues

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Cited by 1 •

2022

Shotgun mass spectrometry-based lipidomics delivers a sensitive quantitative snapshot of a broad spectrum of lipid classes simultaneously in a single measurement from various rodent tissues.

Isolation, Culture and Long-Term Maintenance of Primary Mesencephalic Dopaminergic Neurons From Embryonic Rodent Brains

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Cited by 33 •

2015

The causes of degeneration of midbrain dopaminergic neurons during Parkinson’s disease are not fully understood. Cellular culture systems provide an essential tool for study of the neurophysiological properties of these neurons. Here we present an optimized protocol, which can be utilized for in vitro modeling of neurodegeneration.

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