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用于鼠脑和人脑的突触神经小体的微分离方法,以及原代神经元培养。

Synaptoneurosome micromethod for fractionation of mouse and human brain, and primary neuronal cultures.

机构信息

Department of Neurosurgery, David Geffen School of Medicine at UCLA, Los Angeles, CA 90095, USA.

出版信息

J Neurosci Methods. 2012 Nov 15;211(2):289-95. doi: 10.1016/j.jneumeth.2012.09.005. Epub 2012 Sep 24.

Abstract

Brain and primary neuron fractions enriched in synaptic terminals are important tools for neuroscientists in biochemical, neuroanatomical and physiological studies. We describe an annotated updated micro-method for preparing synaptoneurosomes (SNs) enriched in presynaptic and postsynaptic elements. An easy to follow, step-by-step, protocol is provided for making SNs from small amounts of mammalian brain tissue. This includes novel applications for material obtained from human neurosurgical procedures and primary rat neuronal cultures. Our updated method for preparing SNs using smaller amounts of tissue provides a valuable new tool and expands the capabilities of neuroscientists.

摘要

富含突触末端的脑和原代神经元级分是神经科学家进行生化、神经解剖学和生理学研究的重要工具。我们描述了一种经过注释的更新的微方法,用于制备富含突触前和突触后成分的突触小体(SNs)。我们提供了一个简单易行的分步协议,用于从小鼠脑组织中制备 SNs。这包括从人类神经外科手术和原代大鼠神经元培养物中获得的材料的新应用。我们使用较少组织量制备 SNs 的更新方法提供了一个有价值的新工具,并扩展了神经科学家的能力。

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