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    • 3. 发明授权
    • Purification of urokinase
    • 尿激酶的纯化
    • US4106992A
    • 1978-08-15
    • US628968
    • 1975-11-05
    • Edmond G. VairelJean GoulayJean Choay
    • Edmond G. VairelJean GoulayJean Choay
    • A61K38/00C12N9/72C07G7/02
    • C12N9/6462C12Y304/21073A61K38/00Y10S435/815
    • An initial solution of crude urokinase especially of human origin, is subjected to exclusion chromatography by contact with a DEAE cellulose resin, following adjustment of the pH of the solution to a value of from 4 to 6, and of its conductivity to a value of from 15,000 to 25,000 micromhos. An effluent enriched in urokinase is collected. A urokinase, mixed with foreign proteins, especially pyrogens, is purified by a partial saturation of an aqueous solution of this mixture by ammonium sulphate to a value for which the precipitate formed would not entrain more than 5% of the total activity of urokinase of the initial solution. A supernatant liquid enriched in urokinase is collected . A complex of urokinase and heparin, urokinase heparinate, is made by reacting an enriched solution of urokinase with a solution of heparin. It has relative activities of 30,000 to 100,000 CTA units of urokinase for 100 Iu of heparin. In an isotonic perfusion solution in glucose serum, its dilution is from 300,000 to 900,000 CTA units of urokinase/250 ml.
    • 通过与DEAE纤维素树脂的接触,将溶液的pH值调整至4至6,并将其电导率调节至从 15,000至25,000微镜。 收集富含尿激酶的流出液。 与外来蛋白质,特别是热原混合的尿激酶通过硫酸铵将该混合物的水溶液部分饱和至达到其形成的沉淀物不会夹带大于5%的尿激酶活性的值的纯化 初始解决方案 收集富含尿激酶的上清液。 通过使尿激酶的富集溶液与肝素溶液反应制成尿激酶和肝素复合物,尿激酶尿激酶。 对于100 Iu肝素,它具有30,000至100,000 CTA尿激酶单位的相对活性。 在葡萄糖血清中的等渗灌注溶液中,其稀释度为30,000至900,000 CTA单位的尿激酶/ 250ml。