Fluorescent in situ hybridization of synaptic proteins imaged with super-resolution STED microscopy

Microscopy Research and Technique

Volumn 77, Issue 7, 2014, Pages 517-527

  Zhang, William I ^a,b   Röhse, Heiko ^b,c   Rizzoli, Silvio O ^a,b   Opazo, Felipe ^a,b  

^a UNIVERSITY OF GÖTTINGEN   (Germany)

^b EUROPEAN NEUROSCIENCE INSTITUTE   (Germany)

^c Leica Microsystems GmbH   (Germany)

Author keywords

FISH; Microscopy; MRNA

Indexed keywords

FISH; FLUORESCENCE; FLUORESCENCE MICROSCOPY; NEURONS; NUCLEIC ACIDS; OPTICAL RESOLVING POWER;

CONVENTIONAL IMAGING; FLUORESCENT IN SITU HYBRIDIZATION; LABELINGS; MESSENGER RNA; MRNA; SINGLE NEURON; SUPERRESOLUTION; SUPERRESOLUTION METHODS; SYNAPTIC PROTEINS; TECHNICAL DIFFICULTIES;

PROTEINS;

FLUORESCENT DYE; SYNAPTOBREVIN; SYNAPTOPHYSIN; SYNAPTOTAGMIN;

ANIMAL; CHLOROCEBUS AETHIOPS; COS 1 CELL LINE; CYTOLOGY; DIAGNOSTIC USE; FLUORESCENCE IN SITU HYBRIDIZATION; FLUORESCENCE MICROSCOPY; HIPPOCAMPUS; IMMUNOLOGY; METABOLISM; PROCEDURES; RAT;

ANIMALS; CERCOPITHECUS AETHIOPS; COS CELLS; FLUORESCENT DYES; HIPPOCAMPUS; IN SITU HYBRIDIZATION, FLUORESCENCE; MICROSCOPY, FLUORESCENCE; R-SNARE PROTEINS; RATS; SYNAPTOPHYSIN; SYNAPTOTAGMINS;

EID: 84903130354     PISSN: 1059910X     EISSN: 10970029     Source Type: Journal    
DOI: 10.1002/jemt.22367     Document Type: Article

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