LR White is preferable to Unicryl for immunogold detection of fixation-sensitive nuclear antigens
Jazyk angličtina Země Itálie Médium print
Typ dokumentu srovnávací studie, časopisecké články, práce podpořená grantem
PubMed
12597621
DOI
10.4081/1748
Knihovny.cz E-zdroje
- MeSH
- akrylové pryskyřice * MeSH
- antigeny jaderné chemie izolace a purifikace MeSH
- fixace tkání metody MeSH
- HeLa buňky MeSH
- imunoelektronová mikroskopie MeSH
- imunohistochemie * MeSH
- indikátory a reagencie MeSH
- lidé MeSH
- ultrafialové záření MeSH
- zalévání tkání MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- srovnávací studie MeSH
- Názvy látek
- akrylové pryskyřice * MeSH
- antigeny jaderné MeSH
- indikátory a reagencie MeSH
- LR white MeSH Prohlížeč
- unicryl MeSH Prohlížeč
The purpose of this study was to compare two electron microscopy embedding media - LR White and Unicryl - with regard to cell morphologyical and immunohistochemical preservation properties for the study of fixation-sensitive nuclear antigens. Human cervical carcinoma (HeLa) cells were fixed with 2% paraformaldehyde and 0.1% glutaraldehyde, and embedded in parallel in the two resins: LR White and Unicryl using; two different polymerization protocols were used for each resin. Preservation of fine nuclear structure was good after LR White and poor after Unicryl embedding. Immunogold labeling of Sm antigen was significantly stronger on LR White sections. Polymerization by UV light resulted in stronger and more specific labeling than heat polymerization. These results show that LR White is advantageous over Unicryl for the study of nuclear antigens requiring delicate aldehyde fixation.
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