Kubke Lab:Protocols: Difference between revisions
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=Sectioning= | =General Histology= | ||
==Fixation== | |||
==Embedding== | |||
==Sectioning== | |||
[[Kubke_Lab:Protocols/Cryomicrotomy|Cryostat | [[Kubke_Lab:Protocols/Cryomicrotomy|Cryostat]] | ||
Paraffin Microtome | |||
Sliding microtome | |||
Ultramicrotome | |||
= | =Staining= | ||
==Slide Subbing and mounting== | ==Slide Subbing and mounting== | ||
[[Kubke_Lab:Protocols/Gelatin_Subbing|Gelatin Slide Subbing]] | [[Kubke_Lab:Protocols/Gelatin_Subbing|Gelatin Slide Subbing]] | ||
==Classical Histology== | ==Classical Histology== | ||
[[Kubke_Lab:Protocols/Hematoxylin_Eosin|Hematoxylin Eosin Stain]] | [[Kubke_Lab:Protocols/Hematoxylin_Eosin|Hematoxylin Eosin Stain]] | ||
[[Kubke_Lab:Protocols/Nissl_Stain_Protocol|Cresyl Violet (Nissl Stain)]] | |||
[[Kubke_Lab:Protocols/Nissl_Stain_Protocol|Nissl Stain]] | ==Golgi== | ||
==Immunocytochemistry== | |||
=Tract Tracing= | |||
=Imaging= | |||
==Light Microscopy== | |||
==Epifluorescence microscopy== | |||
==Confocal microscopy== | |||
==Transmission Electron Microscopy== | |||
==Scanning Electron Microscopy== | |||
==CT and micro CT== | |||
==MRI== | |||
=Cell Culture= | |||
==Primary cell cultures in monolayer== | |||
==Primary cell cultures in reaggregates== | |||
=Surgery= | |||
=Embryonic surgery= | |||
=Electrophysiology= | |||
==Intracellular (sharp)== | |||
==Extracellular== | |||
===multiunit=== | |||
===single unit=== | |||
==Evoked potentials== | |||
=Return to [[Kubke_Lab|Kubke Lab Page]]= | =Return to [[Kubke_Lab|Kubke Lab Page]]= | ||
Revision as of 20:11, 25 May 2011
List of Protocol pages. To create a protocol page please use the following naming convention: Kubke_Lab:Protocols/Protocol_name
General Histology
Fixation
Embedding
Sectioning
Cryostat Paraffin Microtome Sliding microtome Ultramicrotome
Staining
Slide Subbing and mounting
Classical Histology
Hematoxylin Eosin Stain Cresyl Violet (Nissl Stain)
