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Tools for visualization of phosphoinositides in the cell nucleus

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68378050%3A_____%2F16%3A00472618" target="_blank" >RIV/68378050:_____/16:00472618 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216208:11310/16:10336679

  • Result on the web

    <a href="http://dx.doi.org/10.1007/s00418-016-1409-8" target="_blank" >http://dx.doi.org/10.1007/s00418-016-1409-8</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1007/s00418-016-1409-8" target="_blank" >10.1007/s00418-016-1409-8</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Tools for visualization of phosphoinositides in the cell nucleus

  • Original language description

    Phosphoinositides (PIs) are glycerol-based phospholipids containing hydrophilic inositol ring. The inositol ring is mono-, bis-, or tris-phosphorylated yielding seven PIs members. Ample evidence shows that PIs localize both to the cytoplasm and to the nucleus. However, tools for direct visualization of nuclear PIs are limited and many studies thus employ indirect approaches, such as staining of their metabolic enzymes. Since localization and mobility of PIs differ from their metabolic enzymes, these approaches may result in incomplete data. In this paper, we tested commercially available PIs antibodies by light microscopy on fixed cells, tested their specificity using protein-lipid overlay assay and blocking assay, and compared their staining patterns. Additionally, we prepared recombinant PIs-binding domains and tested them on both fixed and live cells by light microscopy. The results provide a useful overview of usability of the tools tested and stress that the selection of adequate tools is critical. Knowing the localization of individual PIs in various functional compartments should enable us to better understand the roles of PIs in the cell nucleus.

  • 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

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

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

    Histochemistry and Cell Biology

  • ISSN

    0948-6143

  • e-ISSN

  • Volume of the periodical

    145

  • Issue of the periodical within the volume

    4

  • Country of publishing house

    DE - GERMANY

  • Number of pages

    12

  • Pages from-to

    485-496

  • UT code for WoS article

    000372608900012

  • EID of the result in the Scopus database