Nissl staining: Difference between revisions
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* [http://www.psy.jhu.edu/~fortune/Nissl.html Nissl staining protocol from the Fortune lab, Johns Hopkins] | * [http://www.psy.jhu.edu/~fortune/Nissl.html Nissl staining protocol from the Fortune lab, Johns Hopkins] | ||
* [http://psych.colorado.edu/~dbarth/PDFs/4052/4052%20Manual%20Chapters/Histology%20I.pdf Nissl staining protocol from Barth course material, U of Colorado at Boulder] | * [http://psych.colorado.edu/~dbarth/PDFs/4052/4052%20Manual%20Chapters/Histology%20I.pdf Nissl staining protocol from Barth course material, U of Colorado at Boulder] | ||
* [http://www.neuralstainkit.com/index.php?pr=Ready-to-Use_Staining_Solutions Commercial Nissl staining solutions w photos of stained sections] | |||
[[Category:Material]] | [[Category:Material]] | ||
Latest revision as of 05:48, 20 May 2010
The Nissl staining is a classic nucleic acid staining method traditionally used on nervous tissue sections. The active dye in the staining solution can vary, but toluidine blue or cresyl violet are common components. Nissl is also an outdated term for the ER.
Principle
A basic dye (aniline, thionine, or cresyl violet) binds to negatively charged nucleic acids like RNA and DNA.
Target of the dye
Nissl staining typically marks the ER due to ribosomal RNA as well as the nucleus and other accumulations of nucleic acid.
External links
- Nissl staining section from the biography of the eponymous scientist Franz Nissl in the Wikipedia
- Nissl staining of paraffin section protocol from the Hevner lab U Washington
- Nissl staining protocol from the Fortune lab, Johns Hopkins
- Nissl staining protocol from Barth course material, U of Colorado at Boulder
- Commercial Nissl staining solutions w photos of stained sections
