Laser-capture microdissection.

Details

Serval ID
serval:BIB_6CA8735D22A2
Type
Article: article from journal or magazin.
Collection
Publications
Title
Laser-capture microdissection.
Journal
Nature Protocols
Author(s)
Espina V., Wulfkuhle J.D., Calvert V.S., VanMeter A., Zhou W., Coukos G., Geho D.H., Petricoin E.F., Liotta L.A.
ISSN
1750-2799 (Electronic)
ISSN-L
1750-2799
Publication state
Published
Issued date
2006
Volume
1
Number
2
Pages
586-603
Language
english
Notes
Publication types: Journal ArticlePublication Status: ppublish
Abstract
Deciphering the cellular and molecular interactions that drive disease within the tissue microenvironment holds promise for discovering drug targets of the future. In order to recapitulate the in vivo interactions thorough molecular analysis, one must be able to analyze specific cell populations within the context of their heterogeneous tissue microecology. Laser-capture microdissection (LCM) is a method to procure subpopulations of tissue cells under direct microscopic visualization. LCM technology can harvest the cells of interest directly or can isolate specific cells by cutting away unwanted cells to give histologically pure enriched cell populations. A variety of downstream applications exist: DNA genotyping and loss-of-heterozygosity (LOH) analysis, RNA transcript profiling, cDNA library generation, proteomics discovery and signal-pathway profiling. Herein we provide a thorough description of LCM techniques, with an emphasis on tips and troubleshooting advice derived from LCM users. The total time required to carry out this protocol is typically 1-1.5 h.
Keywords
Cell Separation/instrumentation, Cell Separation/methods, DNA, Infrared Rays, Lasers, Microdissection/instrumentation, Microdissection/methods, Proteins, RNA, Staining and Labeling, Ultraviolet Rays
Pubmed
Create date
14/10/2014 12:43
Last modification date
20/08/2019 15:26
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