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Ultrastructural and nuclear antigen preservation after high-pressure freezing/freeze-substitution and low-temperature LR White embedding of HeLa cells
V Stradalova, K Gaplovska-Kysela, P Hozak
Jazyk angličtina Země Německo
NLK
SpringerLink Journals
od 2005-01-01 do 2008-12-31
ProQuest Central
od 1997-01-01 do 2017-12-31
Medline Complete (EBSCOhost)
od 2000-01-01 do Před 1 rokem
Nursing & Allied Health Database (ProQuest)
od 1997-01-01 do 2017-12-31
Health & Medicine (ProQuest)
od 1997-01-01 do 2017-12-31
Public Health Database (ProQuest)
od 1997-01-01 do 2017-12-31
- MeSH
- akrylové pryskyřice MeSH
- antigeny jaderné analýza MeSH
- buněčné jádro imunologie ultrastruktura MeSH
- financování organizované MeSH
- HeLa buňky MeSH
- imunohistochemie MeSH
- kryoprezervace metody MeSH
- lidé MeSH
- mrazová substituce MeSH
- tlak MeSH
- transmisní elektronová mikroskopie MeSH
- zalévání tkání plastickou hmotou metody MeSH
- Check Tag
- lidé MeSH
A protocol for high-pressure freezing and LR White embedding of mammalian cells suitable for fine ultrastructural studies in combination with immunogold labelling is presented. HeLa S3 cells enclosed in low-temperature gelling agarose were high-pressure frozen, freeze-substituted in acetone, and embedded in LR White at 0 degrees C. The morphology of such cells and the preservation of nuclear antigens were excellent in comparison with chemically fixed cells embedded in the same resin. The immunolabelling signal for different nuclear antigens was 4-to-13 times higher in high-pressure frozen than in chemically fixed cells. We conclude that one can successfully use high-pressure freezing/freeze-substitution and LR White embedding as an alternative of Lowicryl resins.
Citace poskytuje Crossref.org
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