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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
|
pubmed:dateCreated |
1979-7-28
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pubmed:abstractText |
For extraction of soluble antigen from cells infected with Epstein-Barr virus, Herpesvirus salmirl, and H. ateles, 0.1 M glycine (pH 9.5) was used. This method yielded increased amounts of the antigen containing much less cell debris. Lymphoblastoid cells infected with Epstein-Barr virus could maintain up to 50% viability after the extraction procedure. These cells could be used again after an appropriate interval in culture. The usefulness of this technique is discussed.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
0027-8874
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
62
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1173-5
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pubmed:dateRevised |
2001-11-2
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pubmed:meshHeading |
pubmed-meshheading:220447-Antigens, Viral,
pubmed-meshheading:220447-Glycine,
pubmed-meshheading:220447-Herpesviridae,
pubmed-meshheading:220447-Herpesvirus 2, Saimiriine,
pubmed-meshheading:220447-Herpesvirus 4, Human,
pubmed-meshheading:220447-Immunologic Techniques,
pubmed-meshheading:220447-Microbiological Techniques
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pubmed:year |
1979
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pubmed:articleTitle |
Extraction of soluble antigens of Epstein-Barr virus, Herpesvirus salmirl, and Herpesvirus ateles with the use of glycine.
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pubmed:publicationType |
Journal Article
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