DNA from microdissected tissues may be extracted and stored on microscopic slides
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11140%2F16%3A10327067" target="_blank" >RIV/00216208:11140/16:10327067 - isvavai.cz</a>
Alternative codes found
RIV/00216208:11110/16:10327067 RIV/00064165:_____/16:10327067
Result on the web
<a href="http://dx.doi.org/10.4149/neo_2016_404" target="_blank" >http://dx.doi.org/10.4149/neo_2016_404</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.4149/neo_2016_404" target="_blank" >10.4149/neo_2016_404</a>
Alternative languages
Result language
angličtina
Original language name
DNA from microdissected tissues may be extracted and stored on microscopic slides
Original language description
With regard to complex structure of tissues, laser capture microdissection represents an important step in analytical workflow streaming to proper molecular characterization of different cell types in examined samples. Therefore the simple method for simultaneous processing of higher numbers of microdissected tissues leading not only to rapid and efficient DNA isolation but allowing also the repeated sampling and easy storage may be useful in the practice of histopathological laboratories. We elaborated such a methodology applicable downstream after the microdissection from formalin-fixed paraffin embedded tissues. The tissues for examination are microdissected directly into the circular areas having the diameter 2 mm and marked on the microscopic slide. In this way, one slide is able to accommodate multiple samples. The DNA extraction is performed in low volume of buffer with Proteinase Kin a droplet covered by mineral oil just on the slide. Mineral oil in the quality for molecular biology not only avoids evaporation during DNA extraction, but it helps to position the micro disssected tissue, to control the level of cell lysis microscopically and to protect the DNA sample during subsequent manipulations. We provided the evidence that DNA isolated by our methodology remains in the positions on microscopic slide for months without any changes in the lengths of available fragments and that it may be removed from each position repetitively for different kinds of analysis. The new methodological approach presented by us can be practically applied in broad spectrum of laboratories performing routinely genetic analysis on microdissected tissues.
Czech name
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Czech description
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Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
EB - Genetics and molecular biology
OECD FORD branch
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Result continuities
Project
<a href="/en/project/FR-TI1%2F328" target="_blank" >FR-TI1/328: *R and D of certified technologie isolation of DNA from histopatologic material</a><br>
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Others
Publication year
2016
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Neoplasma
ISSN
0028-2685
e-ISSN
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Volume of the periodical
63
Issue of the periodical within the volume
4
Country of publishing house
SK - SLOVAKIA
Number of pages
5
Pages from-to
518-522
UT code for WoS article
000381446700004
EID of the result in the Scopus database
2-s2.0-84978419118