Laser Capture Microdissection of Mammalian Tissue
Robert A Edwards Department of Pathology, University of California, Irvine
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0:00 Title0 0:05 Introduction5 0:21 Subscription Lock21 0:59 Initializing the Instrument for Use59 4:24 Sample Preparation264 5:57 Mounting the Specimen and Setting up Capture Tubes357 8:25 Aligning the Microscope505 11:21 Adjusting the Capture Controls681 15:56 Conclusion956
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Laser capture microscopy, also known as laser microdissection (LMD), enables the user to isolate small numbers of cells or tissues from frozen or formalin-fixed, paraffin-embedded tissue sections. LMD techniques rely on a thermo labile membrane placed either on top of, or underneath, the tissue section. In one method, focused laser energy is used to melt the membrane onto the underlying cells, which can then be lifted out of the tissue section. In the other, the laser energy vaporizes the foil along a path "drawn" on the tissue, allowing the selected cells to fall into a collection device. Each technique allows the selection of cells with a minimum resolution of several microns. DNA, RNA, protein, and lipid samples may be isolated and analyzed from micro-dissected samples. In this video, we demonstrate the use of the Leica AS-LMD laser microdissection instrument in seven segments, including an introduction to the principles of LMD, initializing the instrument for use, general considerations for sample preparation, mounting the specimen and setting up capture tubes, aligning the microscope, adjusting the capture controls, and capturing tissue specimens. Laser-capture micro-dissection enables the investigator to isolate samples of pure cell populations as small as a few cell-equivalents. This allows the analysis of cells of interest that are free of neighboring contaminants, which may confound experimental results.
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Edwards RA (2007). Laser Capture Microdissection of Mammalian Tissue. JoVE. 8. http://www.jove.com/index/details.stp?id=309, doi: 10.3791/309
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| | 03/20/2008 12:24:15 AM
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Ratan responded with a statement of type: Neutral
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Hi, I am facing problem with RNA isolation of microdissected slides. Frist I staine sections using std protocol of H&E stain (we filter it using Nalgene filter) and then do dissection for 45 minutes, cutting more than 1500 cells. Later RNA is isolated using RNAeasy Micro kit (qiagen). My problem is cutting cells (objects) less than 500 is not detected by Agilent bioanalyser pico chip. And RNA concentratin is too low (1400pg/14ul in 700 cells) to be detected in bioanalyser. Can u suggest me what should I do to enhance RNA integrity number (RIN), ration of 28s/18s as well as concentration of it. I wonder how to detect RNA in sample having 20-50 cells only. Any suggestion at this point will be greately appreciated. Thanks in advance Ratan
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