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    • 5. 发明授权
    • Method and kit for determination of prostacyclin in plasma
    • 血浆前列环素测定方法及试剂盒
    • US07659078B1
    • 2010-02-09
    • US10620806
    • 2003-07-17
    • Sylvia DaunertMichael PoonUrvee DesaiSapna K. Deo
    • Sylvia DaunertMichael PoonUrvee DesaiSapna K. Deo
    • G01N33/53G01N33/537G01N33/543G01N33/88C12Q1/66C07K16/18C07K16/26
    • G01N33/88G01N2800/12Y10S435/971Y10S435/975Y10S530/807
    • A solid-phase immunoassay for 6-keto-Prostaglandin F1α, the stable hydrolysis product of prostacyclin (Prostaglandin I2) is disclosed. Prostacyclin, a potent vasodilator with anti-platelet and anti-proliferative properties is an effective treatment for primary pulmonary hypertension and pulmonary arterial hypertension associated with scleroderma and scleroderma-like syndrome. Levels of 6-keto-Prostaglandin F1α can be directly correlated with levels of prostacyclin. Therefore, 6-keto-Prostaglandin F1α has become the indicator of choice to measure prostacyclin levels. The single step immunoassay for 6-keto-Prostaglandin F1α uses the bioluminescent protein, aequorin as a label. Analyte-label conjugates were constructed by linking the carboxyl group of 6-keto-Prostaglandin F1α and lysine residues of aequorin by chemical conjugation methods. The binding properties of 6-keto-Prostaglandin F1α towards its antibody and the bioluminescent properties of aequorin are retained in the conjugate. The concentration of 6-keto-Prostaglandin F1α after extraction from plasma shows good correlation with the concentration of 6-keto-Prostaglandin F1α obtained without prior extraction of the same plasma sample. The assay allows the measurement of 6-keto-Prostaglandin F1α directly in plasma without any pre-treatment of the samples, which results in a much simpler method with a faster assay time.
    • 公开了前列环素(前列腺素I2)的稳定水解产物6-酮 - 前列腺素F1alpha的固相免疫测定。 前列环素,具有抗血小板和抗增殖特性的强效血管扩张剂是与硬皮病和硬皮病样综合征相关的原发性肺动脉高压和肺动脉高压的有效治疗方法。 6-keto-Prostaglandin F1alpha的水平可以与前列环素的水平直接相关。 因此,6-keto-Prostaglandin F1alpha已经成为衡量前列环素水平的首选指标。 6-keto-Prostaglandin F1alpha的单步免疫测定使用生物发光蛋白,水母发光蛋白作为标记。 通过化学共轭方法连接6-酮基前列腺素F1al的羧基和水母发光蛋白的赖氨酸残基,构建了分析标记物缀合物。 6-酮前列腺素F1alpha对其抗体的结合性质和水母发光蛋白的生物发光性质保留在缀合物中。 从血浆中提取6-keto-Prostaglandin F1alpha的浓度与未经提取相同血浆样品的6-酮 - 前列腺素F1al的浓度呈现良好的相关性。 该测定允许直接在血浆中测量6-酮基前列腺素F1alpha,而没有对样品进行任何预处理,这导致以更快的测定时间简单的方法。