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Electron microscopy in situ hybridization: tracking of DNA and RNA sequences at high resolution
Cmarko D, Koberna K.
Jazyk angličtina Země Spojené státy americké
Typ dokumentu srovnávací studie
- MeSH
- Cercopithecus aethiops MeSH
- COS buňky MeSH
- denaturace nukleových kyselin MeSH
- deoxyribonukleasa I MeSH
- DNA genetika ultrastruktura MeSH
- elektronová kryomikroskopie metody MeSH
- elektronová mikroskopie metody MeSH
- endopeptidasa K MeSH
- financování organizované MeSH
- fixativa MeSH
- geny rRNA MeSH
- HeLa buňky MeSH
- HIV-1 genetika MeSH
- hybridizace in situ metody MeSH
- lidé MeSH
- mikrotomie metody MeSH
- molekulární sondy MeSH
- pankreatická ribonukleasa MeSH
- RNA virová genetika ultrastruktura MeSH
- RNA genetika ultrastruktura MeSH
- zalévání tkání plastickou hmotou MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- zvířata MeSH
- Publikační typ
- srovnávací studie MeSH
Electron microscopy in situ hybridization (EM-ISH) represents a powerful method that enables the localization of specific sequences of nucleic acids at high resolution. We provide here an overview of three different nonisotopic EM-ISH approaches that allow the visualization of nucleic acid sequences in cells. A comparison of various methods with respect to their sensitivity and the structural preservation of the sample is presented, with the aim of helping the reader to choose a convenient hybridization procedure. The post-embedding EM-ISH protocol that currently represents the most widely used technique is described in detail, with a special emphasis on the organization of the cell nucleus.
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