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Generation of Single-Cell Suspensions from Mouse Neural Tissue
Author(s) -
Sandra Pennartz,
Sandy Reiß,
Rebecca Biloune,
Doris Hasselmann,
Andreas Bosio
Publication year - 2009
Publication title -
journal of visualized experiments
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.596
H-Index - 91
ISSN - 1940-087X
DOI - 10.3791/1267
Subject(s) - cell , neural cell , epitope , cell type , spinal cord , chemistry , schwann cell , myelin , microbiology and biotechnology , antigen , central nervous system , biology , neuroscience , biochemistry , immunology
Within the nervous system, hundreds of neuronal and glial cell types have been described. Each specific cell type in the brain or spinal cord has a repertoire of cell surface molecules, or molecular determinants, through which it can be identified and characterized. Currently, robust cell identification and separation technologies require single-cell preparations to be generated while simultaneously limiting cell death and destruction of characteristic surface protein. The gentleMACS Dissociator, when used in combination with trypsin or papain-based dissociation kits, can effectively and gently dissociate brain tissue while preserving antigen epitopes and limiting cell loss. Standardized preparation of single-cell suspensions is achieved using C Tubes and optimized, preset gentleMACS Programs. Once generated, single-cell suspensions can be treated with monoclonal conjugates like Anti-Prominin-1 MicroBeads, which identify neural progenitors, or purified further using Myelin Removal Beads.

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