| pubmed-article:3031657 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:3031657 | lifeskim:mentions | umls-concept:C0677626 | lld:lifeskim |
| pubmed-article:3031657 | lifeskim:mentions | umls-concept:C0040048 | lld:lifeskim |
| pubmed-article:3031657 | lifeskim:mentions | umls-concept:C0204727 | lld:lifeskim |
| pubmed-article:3031657 | lifeskim:mentions | umls-concept:C0205409 | lld:lifeskim |
| pubmed-article:3031657 | lifeskim:mentions | umls-concept:C1999216 | lld:lifeskim |
| pubmed-article:3031657 | pubmed:issue | 7 | lld:pubmed |
| pubmed-article:3031657 | pubmed:dateCreated | 1987-5-4 | lld:pubmed |
| pubmed-article:3031657 | pubmed:abstractText | Progressive inhibition of tissue factor activity occurs upon its addition to human plasma (serum). This process requires the presence of factor VII(a), facto-X(a), Ca2+, and another component in plasma that we have called the tissue factor inhibitor (TFI). A TFI secreted by HepG2 cells (human hepatoma cell line) was isolated from serum-free conditioned medium in a four-step procedure including CdCl2 precipitation, diisopropylphosphoryl-factor Xa affinity chromatography, Sephadex G-75 superfine gel filtration, and Mono Q ion-exchange chromatography. The purified TFI contained a predominant band at Mr 38,000 on NaDodSO4/polyacrylamide gel electrophoresis that comigrates with inhibitory activity. Like the activity present in plasma, this TFI requires the presence of factor VII(a), factor X(a), and Ca2+ to express inhibitory activity. Its specific activity (assuming an extinction coefficient of 10 at 280 nM, for a 1-cm path length through a 1% solution) was 9800 units/mg of protein, where 1 unit of TFI activity was defined as that present in 1 ml of normal pooled serum. | lld:pubmed |
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| pubmed-article:3031657 | pubmed:language | eng | lld:pubmed |
| pubmed-article:3031657 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:3031657 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:3031657 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:3031657 | pubmed:month | Apr | lld:pubmed |
| pubmed-article:3031657 | pubmed:issn | 0027-8424 | lld:pubmed |
| pubmed-article:3031657 | pubmed:author | pubmed-author:MiletichJ PJP | lld:pubmed |
| pubmed-article:3031657 | pubmed:author | pubmed-author:BrozeG JGJJr | lld:pubmed |
| pubmed-article:3031657 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:3031657 | pubmed:volume | 84 | lld:pubmed |
| pubmed-article:3031657 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:3031657 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:3031657 | pubmed:pagination | 1886-90 | lld:pubmed |
| pubmed-article:3031657 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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| pubmed-article:3031657 | pubmed:year | 1987 | lld:pubmed |
| pubmed-article:3031657 | pubmed:articleTitle | Isolation of the tissue factor inhibitor produced by HepG2 hepatoma cells. | lld:pubmed |
| pubmed-article:3031657 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:3031657 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
| pubmed-article:3031657 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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