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    • 7. 发明授权
    • Chronic fatigue syndrome diagnosis
    • 慢性疲劳综合征诊断
    • US06214554B1
    • 2001-04-10
    • US09296211
    • 1999-04-21
    • Robert J. Suhadolnik
    • Robert J. Suhadolnik
    • C12Q168
    • C12Q1/34G01N33/573G01N2333/922
    • Chronic fatigue syndrome is diagnosed through detection of an about 30 kDa RNase L molecule under native conditions in cellular extracts of RNase L-containing cells such as peripheral blood mononuclear cells. Proteins are fractionated according to molecular weight under nondenaturing conditions. The fractionated proteins are assayed for the presence of the about 30 kDa protein having 2-5A-dependent RNase L enzyme activity. The severity of the affliction may be determined by testing for the presence of RNase L molecules having approximate molecular weights of 30 and 80 kDa. The presence of the about 30 kDa RNase L, and the absence of the about 80 kDa RNase L molecule, correlates with severe chronic fatigue syndrome. The presence of both RNase L molecules indicates a less severe chronic fatigue syndrome affliction. Under denaturing conditions, and in the presence of protease inhibitors, chronic fatigue syndrome may be diagnosed through the detection of an about 37 kDa 2-5A binding protein.
    • 通过在天然条件下检测约30kDa的RNA酶L分子来诊断慢性疲劳综合征,在含有RNase L的细胞例如外周血单核细胞的细胞提取物中。 蛋白质在非变性条件下根据分子量分级。 测定分级蛋白质是否存在具有2-5A依赖性RNA酶L酶活性的约30kDa蛋白质。 可以通过测试具有近似分子量为30和80kDa的RNA酶L分子的存在来确定苦难的严重程度。 约30kDa核糖核酸酶L的存在和约80kDa核糖核酸酶L分子的不存在与严重的慢性疲劳综合征相关。 两种RNase L分子的存在表明不太严重的慢性疲劳综合症患者。 在变性条件下,并且在蛋白酶抑制剂存在下,可以通过检测约37kDa 2-5A结合蛋白来诊断慢性疲劳综合征。
    • 8. 发明授权
    • Chronic fatigue syndrome diagnosis
    • 慢性疲劳综合征诊断
    • US5985565A
    • 1999-11-16
    • US895120
    • 1997-07-16
    • Robert J. Suhadolnik
    • Robert J. Suhadolnik
    • C12Q1/34C12Q1/68G01N33/573
    • C12Q1/34G01N33/573G01N2333/922
    • Chronic fatigue syndrome is diagnosed through detection of an about 30 kDa RNase L molecule under native conditions in cellular extracts of RNase L-containing cells such as peripheral blood mononuclear cells. Proteins are fractionated according to molecular weight under nondenaturing conditions. The fractionated proteins are assayed for the presence of the about 30 kDa protein having 2-5A-dependent RNase L enzyme activity. The severity of the affliction may be determined by testing for the presence of RNase L molecules having approximate molecular weights of 30 and 80 kDa. The presence of the about 30 kDa RNase L, and the absence of the about 80 kDa RNase L molecule, correlates with severe chronic fatigue syndrome. The presence of both RNase L molecules indicates a less severe chronic fatigue syndrome affliction. Under denaturing conditions, and in the presence of protease inhibitors, chronic fatigue syndrome may be diagnosed through the detection of an about 37 kDa 2-5A binding protein.
    • 通过在天然条件下检测约30kDa的RNA酶L分子来诊断慢性疲劳综合征,在含有RNase L的细胞例如外周血单核细胞的细胞提取物中。 蛋白质在非变性条件下根据分子量分级。 测定分级蛋白质是否存在具有2-5A依赖性RNA酶L酶活性的约30kDa蛋白质。 可以通过测试具有近似分子量为30和80kDa的RNA酶L分子的存在来确定苦难的严重程度。 约30kDa核糖核酸酶L的存在和约80kDa核糖核酸酶L分子的不存在与严重的慢性疲劳综合征相关。 两种RNase L分子的存在表明不太严重的慢性疲劳综合症患者。 在变性条件下,并且在蛋白酶抑制剂存在下,可以通过检测约37kDa 2-5A结合蛋白来诊断慢性疲劳综合征。