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Electrophoretic mobility of cardiac myosin heavy chain isoforms revisited: application of MALDI TOF/TOF analysis
P. Arnostova, PL. Jedelsky, T. Soukup, J. Zurmanova,
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články, práce podpořená grantem
NLK
Free Medical Journals
od 2001
PubMed Central
od 2001 do 2012
Europe PubMed Central
od 2001 do 2012
ProQuest Central
od 2007-01-01 do 2012
Open Access Digital Library
od 2001-01-01 do 2012-11-27
Open Access Digital Library
od 2001-01-01 do 2012-12-31
Open Access Digital Library
od 2001-01-01
CINAHL Plus with Full Text (EBSCOhost)
od 2006-01-01 do 2012-01-31
Medline Complete (EBSCOhost)
od 2006-01-01 do 2012-01-31
Health & Medicine (ProQuest)
od 2007-01-01 do 2012
ROAD: Directory of Open Access Scholarly Resources
od 2000 do 2012
PubMed
22187528
DOI
10.1155/2011/634253
Knihovny.cz E-zdroje
- MeSH
- elektroforéza v polyakrylamidovém gelu metody MeSH
- hypertyreóza metabolismus MeSH
- hypotyreóza metabolismus MeSH
- komorové myosiny chemie izolace a purifikace metabolismus MeSH
- krysa rodu rattus MeSH
- molekulární sekvence - údaje MeSH
- potkani inbrední LEW MeSH
- protein - isoformy MeSH
- sekvence aminokyselin MeSH
- sekvenční seřazení MeSH
- spektrometrie hmotnostní - ionizace laserem za účasti matrice metody MeSH
- těžké řetězce myosinu chemie izolace a purifikace metabolismus MeSH
- western blotting MeSH
- zvířata MeSH
- Check Tag
- krysa rodu rattus MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
The expression of two cardiac myosin heavy chain (MyHC) isoforms in response to the thyroid status was studied in left ventricles (LVs) of Lewis rats. Major MyHC isoform in euthyroid and hyperthyroid LVs had a higher mobility on SDS-PAGE, whereas hypothyroid LVs predominantly contained a MyHC isoform with a lower mobility corresponding to that of the control soleus muscle. By comparing the MyHC profiles obtained under altered thyroid states together with the control soleus, we concluded that MyHCα was represented by the lower band with higher mobility and MyHCβ by the upper band. The identity of these two bands in SDS-PAGE gels was confirmed by western blot and mass spectrometry. Thus, in contrast to the literature data, we found that the MyHCα possessed a higher mobility rate than the MyHCβ isoform. Our data highlighted the importance of the careful identification of the MyHCα and MyHCβ isoforms analyzed by the SDS-PAGE.
Citace poskytuje Crossref.org
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