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Merck

Isolation and Maintenance of Murine Embryonic Striatal Neurons.

Bio-protocol (2018-04-20)
Luana Naia, A Cristina Rego
ABSTRACT

Primary cultures of murine striatal neurons are widely used to explore cellular mechanisms in neurobiology, including brain diseases. Here we describe a detailed and standardized protocol to dissect and culture embryonic murine striatal neurons GABA-positive/DARPP-32-positive for 12 days in vitro, when they show good neuronal cell connectivity and the presence of dendritic spines, which reflects the maturation of the network.

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Sigma-Aldrich
HEPES, ≥99.5% (titration)
Sigma-Aldrich
Desossiribonucleasi I, Type IV, lyophilized powder, ≥2,000 Kunitz units/mg protein
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Sieroalbumina, lyophilized powder, essentially fatty acid free, ≥96% (agarose gel electrophoresis)
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5-Fluoro-2′-deoxyuridine, thymidylate synthase inhibitor
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Inibitore della tripsina, lyophilized powder
Sigma-Aldrich
Tripsina, Type IX-S, lyophilized powder, 13,000-20,000 BAEE units/mg protein
Sigma-Aldrich
Anti-GABA antibody produced in rabbit, affinity isolated antibody, buffered aqueous solution