Difference between revisions of "Nissl staining"

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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]
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* [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 04:48, 20 May 2010

Nissl staining (blue) in the substantia nigra pars compacta of mice from (Pan-Montojo 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 Nissl is also an outdated term for the ER.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