| Literature DB >> 20869543 |
Kent McDonald1, Heinz Schwarz, Thomas Müller-Reichert, Rick Webb, Christopher Buser, Mary Morphew.
Abstract
High-pressure freezing (HPF) has been around since the mid-1980s as a cryopreparation technique for biological electron microscopy. It has taken quite some time to "catch on" but with the recent interest in cellular tomography and electron microscopy of vitreous cryosections it has been used more frequently. While HPF is relatively easy to do, there are a number of steps, such as loading the sample into the specimen carrier correctly, that are critical to the success of this method. In this chapter we discuss some of the "little" things that can make the difference between successful or unsuccessful freezing. We cover all aspects of HPF, from specimen loading to removing your sample from the carriers in polymerized resin. Our goal is to make it easier and more reliable for HPF users to get well-frozen samples for their research.Mesh:
Year: 2010 PMID: 20869543 DOI: 10.1016/S0091-679X(10)96028-7
Source DB: PubMed Journal: Methods Cell Biol ISSN: 0091-679X Impact factor: 1.441