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A robust activity marking system for exploring active neuronal ensembles.

eLife (2016-09-24)
Andreas T Sørensen, Yonatan A Cooper, Michael V Baratta, Feng-Ju Weng, Yuxiang Zhang, Kartik Ramamoorthi, Robin Fropf, Emily LaVerriere, Jian Xue, Andrew Young, Colleen Schneider, Casper René Gøtzsche, Martin Hemberg, Jerry Cp Yin, Steven F Maier, Yingxi Lin
ZUSAMMENFASSUNG

Understanding how the brain captures transient experience and converts it into long lasting changes in neural circuits requires the identification and investigation of the specific ensembles of neurons that are responsible for the encoding of each experience. We have developed a Robust Activity Marking (RAM) system that allows for the identification and interrogation of ensembles of neurons. The RAM system provides unprecedented high sensitivity and selectivity through the use of an optimized synthetic activity-regulated promoter that is strongly induced by neuronal activity and a modified Tet-Off system that achieves improved temporal control. Due to its compact design, RAM can be packaged into a single adeno-associated virus (AAV), providing great versatility and ease of use, including application to mice, rats, flies, and potentially many other species. Cre-dependent RAM, CRAM, allows for the study of active ensembles of a specific cell type and anatomical connectivity, further expanding the RAM system's versatility.

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Monoklonaler Anti-GFAP-Antikörper (Glial Fibrillary Acidic Protein, Saures Gliafaserprotein) in Maus hergestellte Antikörper, clone G-A-5, ascites fluid
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Monoklonaler Anti-MAP2 in Maus hergestellte Antikörper, clone HM-2, purified from hybridoma cell culture
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Anti-Parvalbumin-Antikörper, ascites fluid, clone PARV-19, Chemicon®
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Anti-Glutamatrezeptor 2/3-Antikörper, Chemicon®, from rabbit