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Staining protocol for organotypic hippocampal slice cultures
by
DePaola, Vincenzo
, Caroni, Pico
, Gogolla, Nadine
, Galimberti, Ivan
in
Analytical Chemistry
/ Animals
/ Biological Techniques
/ Biomedical and Life Sciences
/ Cell transformation
/ Computational Biology/Bioinformatics
/ Hippocampus
/ Immunohistochemistry - methods
/ Life Sciences
/ Methods
/ Mice
/ Microarrays
/ Organic Chemistry
/ Physiological aspects
/ Protocol
/ Stains and staining (Microscopy)
/ Synapses
/ Tissue Fixation - methods
2006
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Staining protocol for organotypic hippocampal slice cultures
by
DePaola, Vincenzo
, Caroni, Pico
, Gogolla, Nadine
, Galimberti, Ivan
in
Analytical Chemistry
/ Animals
/ Biological Techniques
/ Biomedical and Life Sciences
/ Cell transformation
/ Computational Biology/Bioinformatics
/ Hippocampus
/ Immunohistochemistry - methods
/ Life Sciences
/ Methods
/ Mice
/ Microarrays
/ Organic Chemistry
/ Physiological aspects
/ Protocol
/ Stains and staining (Microscopy)
/ Synapses
/ Tissue Fixation - methods
2006
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While trying to remove the title from your shelf something went wrong :( Kindly try again later!
Do you wish to request the book?
Staining protocol for organotypic hippocampal slice cultures
by
DePaola, Vincenzo
, Caroni, Pico
, Gogolla, Nadine
, Galimberti, Ivan
in
Analytical Chemistry
/ Animals
/ Biological Techniques
/ Biomedical and Life Sciences
/ Cell transformation
/ Computational Biology/Bioinformatics
/ Hippocampus
/ Immunohistochemistry - methods
/ Life Sciences
/ Methods
/ Mice
/ Microarrays
/ Organic Chemistry
/ Physiological aspects
/ Protocol
/ Stains and staining (Microscopy)
/ Synapses
/ Tissue Fixation - methods
2006
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Staining protocol for organotypic hippocampal slice cultures
Journal Article
Staining protocol for organotypic hippocampal slice cultures
2006
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Overview
This protocol details a method to immunostain organotypic slice cultures from mouse hippocampus. The cultures are based on the interface method, which does not require special equipment, is easy to execute and yields slice cultures that can be imaged repeatedly, from the time of isolation at postnatal day 6–9 up to 6 months
in vitro
. The preserved tissue architecture facilitates the analysis of defined hippocampal synapses, cells and entire projections. Time-lapse imaging is based on transgenes expressed in the mice or on constructs introduced through transfection or viral vectors; it can reveal processes that develop over periods ranging from seconds to months. Subsequent to imaging, the slices can be processed for immunocytochemistry to collect further information about the imaged structures. This protocol can be completed in 3 d.
Publisher
Nature Publishing Group UK,Nature Publishing Group
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