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    • 2. 发明授权
    • Method of screening oxysterol activation of LXRα
    • 氧化固醇激活LXRα的方法
    • US06893830B1
    • 2005-05-17
    • US09603131
    • 2000-06-23
    • Bethany A. JanowskiDavid John Mangelsdorf
    • Bethany A. JanowskiDavid John Mangelsdorf
    • G01N33/53G01N33/566G01N33/74G01N33/92
    • G01N33/566G01N33/74G01N33/92
    • The present invention provides a method of screening for agonists of an oxycholesterol activator of LXRα transcription, comprising the steps of: introducing a reporter construct and an LXR expression construct into a host cell; treating the host cell with potential LXR-specific ligands; and identifying compounds which activate LXRα transcription. Also provided is a method of screening for antagonists of an oxycholesterol activator of LXRα transcription, comprising the steps of: introducing a reporter construct and an LXR expression construct into a host cell; pretreating the host cell with activators of LXRα transcription; contacting the host cell with potential antagonists of LXRα transcription; and identifying compounds which block the activation the LXRα transcription.
    • 本发明提供了筛选LXRα转录的氧化胆固醇激活剂的激动剂的方法,包括以下步骤:将报道构建体和LXR表达构建体引入宿主细胞; 用潜在的LXR特异性配体处理宿主细胞; 并鉴定激活LXRα转录的化合物。 还提供了筛选LXRα转录的氧化胆固醇激活剂的拮抗剂的方法,包括以下步骤:将报道构建体和LXR表达构建体引入宿主细胞; 用LXRα转录激活剂预处理宿主细胞; 使宿主细胞与LXRα转录的潜在拮抗剂接触; 并鉴定阻断LXRα转录激活的化合物。