Multiple Mouse Imaging

Multiple Mouse Imaging is an experimental approach that captures biological signals from more than one mouse, enabling parallel analysis of neural structure or activity in neuroscience research. The method coordinates animal positioning, imaging conditions, and image acquisition across subjects so measurements can be compared under consistent experimental settings, while repeated imaging can track changes over time. By increasing throughput and reducing variability between separate experiments, multiple mouse imaging supports studies of brain function, disease progression, behavioral responses, and treatment effects. It can also strengthen statistical analyses by generating datasets from several animals within the same imaging workflow.

Multiple Mouse Imaging - Related Videos

Research

JoVE Journal - Neuroscience
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Multiple-mouse Neuroanatomical Magnetic Resonance Imaging

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Cited by 59 •

2011

Magnetic resonance imaging (MRI) has become an increasingly popular tool for examining the phenotype of genetically altered mice. This article illustrates the methods necessary to achieve high-throughput phenotyping of genetically altered mice using multiple-mouse MRI.

Research

JoVE Journal - Neuroscience

Measuring Progressive Neurological Disability in a Mouse Model of Multiple Sclerosis

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Cited by 21 •

2016

An optimized testing protocol is presented in this paper for the Rotarod performance test, used for measuring progressive neurological disability in TMEV-infected mice.

Non-invasive Optical Imaging of the Lymphatic Vasculature of a Mouse

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Cited by 25 •

2013

Recently developed imaging techniques using near-infrared fluorescence (NIRF) may help elucidate the role the lymphatic system plays in cancer metastasis, immune response, wound repair, and other lymphatic-associated diseases.

Isolation of Multiple Cell Types from a Mouse Brain by Mechanical Homogenization

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2025

This video demonstrates the isolation of multiple types of cells from mouse brain tissue. Tissue is first mechanically sheared using a tissue grinder in a salt solution to maintain an osmotic balance. The tissue homogenate is then subjected to density gradient centrifugation to remove cellular debris. Cells are then resuspended in a solution for further analysis.

Bioluminescence and Near-infrared Imaging of Optic Neuritis and Brain Inflammation in the EAE Model of Multiple Sclerosis in Mice

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Cited by 4 •

2017

We show a technique for in vivo live bioluminescence and near-infrared imaging of optic neuritis and encephalitis in the experimental autoimmune encephalomyelitis (EAE) model for multiple sclerosis in SJL/J mice.

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