Abstract:
:By using affinity-purified antibodies to H10 and to H1AB the localization of these histones was studied by indirect immunofluorescence in the nuclei of proliferating (EAT and uninduced Friend cells) and of differentiating (induced Friend cells) cell populations. While with H1AB antibodies a bright fluorescence all over the chromatin was obtained, the localization of H10 varied depending on the state of the cell population. In the proliferating EAT cells it was localized strictly in the nucleoli. The Friend cell population revealed a heterogeneous picture with two types of H10 localization-nucleolar predominating in uninduced cell populations and peripheral predominating in induced cells. A comparison with literature data suggests that H10 seems to be associated with chromatin regions containing active genes.
journal_name
Exp Cell Resjournal_title
Experimental cell researchauthors
Banchev T,Srebreva L,Zlatanova J,Tsanev Rdoi
10.1016/0014-4827(88)90019-5subject
Has Abstractpub_date
1988-07-01 00:00:00pages
1-8issue
1eissn
0014-4827issn
1090-2422pii
0014-4827(88)90019-5journal_volume
177pub_type
杂志文章abstract::Recent studies have demonstrated a central role for the exchange protein activated by cAMP (Epac) in the inhibition of Fcgamma-receptor-mediated phagocytosis and bacterial killing by prostaglandin E(2) (PGE(2)) in macrophages. However, the subcellular localization of Epac, and its primary target Rap1, has yet to be de...
journal_title:Experimental cell research
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journal_title:Experimental cell research
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journal_title:Experimental cell research
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doi:10.1016/j.yexcr.2008.03.001
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pub_type: 杂志文章
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journal_title:Experimental cell research
pub_type: 杂志文章
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journal_title:Experimental cell research
pub_type: 杂志文章
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pub_type: 杂志文章
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