Novel method of simultaneous multiple immunogold localization on resin sections in high resolution scanning electron microscopy
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11310%2F16%3A10371535" target="_blank" >RIV/00216208:11310/16:10371535 - isvavai.cz</a>
Nalezeny alternativní kódy
RIV/60077344:_____/16:00461980 RIV/60076658:12310/16:43890612
Výsledek na webu
<a href="http://dx.doi.org/10.1016/j.nano.2015.09.008" target="_blank" >http://dx.doi.org/10.1016/j.nano.2015.09.008</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.nano.2015.09.008" target="_blank" >10.1016/j.nano.2015.09.008</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Novel method of simultaneous multiple immunogold localization on resin sections in high resolution scanning electron microscopy
Popis výsledku v původním jazyce
We present a new method of multiple immunolabeling that is suitable for a broad spectrum of biomedical applications. The general concept is to label both sides of the ultrathin section with the thickness of 70-80 nm with different antibodies conjugated to gold nanoparticles and to distinguish the labeled side by advanced imaging methods with high resolution scanning electron microscopy, such as by correlating images acquired at different energies of primary electrons using different signals. From the Clinical Editor: The use of transmission electron microscopy has become an indispensible tool in the detection of cellular proteins. In this short but interesting article, the authors described their new method of labeling and the identification of four different proteins simultaneously, which represents another advance in imaging technique.
Název v anglickém jazyce
Novel method of simultaneous multiple immunogold localization on resin sections in high resolution scanning electron microscopy
Popis výsledku anglicky
We present a new method of multiple immunolabeling that is suitable for a broad spectrum of biomedical applications. The general concept is to label both sides of the ultrathin section with the thickness of 70-80 nm with different antibodies conjugated to gold nanoparticles and to distinguish the labeled side by advanced imaging methods with high resolution scanning electron microscopy, such as by correlating images acquired at different energies of primary electrons using different signals. From the Clinical Editor: The use of transmission electron microscopy has become an indispensible tool in the detection of cellular proteins. In this short but interesting article, the authors described their new method of labeling and the identification of four different proteins simultaneously, which represents another advance in imaging technique.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
30224 - Radiology, nuclear medicine and medical imaging
Návaznosti výsledku
Projekt
—
Návaznosti
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Ostatní
Rok uplatnění
2016
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Nanomedicine: Nanotechnology, Biology, and Medicine
ISSN
1549-9634
e-ISSN
—
Svazek periodika
12
Číslo periodika v rámci svazku
1
Stát vydavatele periodika
NL - Nizozemsko
Počet stran výsledku
4
Strana od-do
105-108
Kód UT WoS článku
000371800600010
EID výsledku v databázi Scopus
2-s2.0-84957064578