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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

  • Czech description

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

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

  • 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