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    • 1. 发明授权
    • Method of irradiating biological specimens
    • 辐射生物标本的方法
    • US5288647A
    • 1994-02-22
    • US686491
    • 1991-04-17
    • William C. Zimlich, Jr.Joseph A. Sorge
    • William C. Zimlich, Jr.Joseph A. Sorge
    • C07K17/00C12Q1/68G01J1/04
    • C07K17/00C12Q1/68Y10T436/25
    • A method of irradiating a biological specimen with ultraviolet, in particular a polynucleotide specimen selected from DNA or RNA, or optionally a protein. In the case where the specimen is DNA or RNA, or potentially proteins, the specimen is irradiated to cross-link the specimen to a substrate. In the case where the specimen is DNA, the specimen can also be irradiated to form thymine dimers. The method uses an apparatus which permits relatively precise control of the total ultraviolet dose received by the specimen, despite any changes of ultraviolet flux from the lamps which may occur from during any one experiment, or between a number of experiments. Thus, the method allows relatively highly reproducible results to be obtained.
    • 用紫外线照射生物样本的方法,特别是选自DNA或RNA的多核苷酸标本,或任选的蛋白质。 在标本是DNA或RNA或潜在的蛋白质的情况下,照射样品以将样品交联到基底上。 在标本为DNA的情况下,也可以照射样品以形成胸腺嘧啶二聚体。 该方法使用允许相对精确地控制由样品接收的总紫外线剂量的装置,尽管在任何一个实验期间或在多个实验之间可能发生来自灯的紫外线通量的任何变化。 因此,该方法允许获得相对高度可重复的结果。
    • 2. 发明授权
    • Method of irradiating biological specimens
    • 辐射生物标本的方法
    • US5814523A
    • 1998-09-29
    • US896717
    • 1997-07-18
    • William C. Zimlich, Jr.Joseph A. Sorge
    • William C. Zimlich, Jr.Joseph A. Sorge
    • C07K17/00C12Q1/68G01J1/04
    • C07K17/00C12Q1/68Y10T436/25
    • A method of irradiating a biological specimen with ultraviolet, in particular a polynucleotide specimen selected from DNA or RNA, or optionally a protein. In the case where the specimen is DNA or RNA, or potentially proteins, the specimen is irradiated to cross-link the specimen to a substrate. In the case where the specimen is DNA, the specimen can also be irradiated to form thymine dimers. The method uses an apparatus which permits relatively precise control of the total ultraviolet dose received by the specimen, despite any changes of ultraviolet flux from the lamps which may occur from during any one experiment, or between a number of experiments. Thus, the method allows relatively highly reproducible results to be obtained.
    • 用紫外线照射生物样本的方法,特别是选自DNA或RNA的多核苷酸标本,或任选的蛋白质。 在标本是DNA或RNA或潜在的蛋白质的情况下,照射样品以将样品交联到基底上。 在标本为DNA的情况下,也可以照射样品以形成胸腺嘧啶二聚体。 该方法使用允许相对精确地控制由样品接收的总紫外线剂量的装置,尽管在任何一个实验期间或在多个实验之间可能发生来自灯的紫外线通量的任何变化。 因此,该方法允许获得相对高度可重复的结果。
    • 3. 发明授权
    • Apparatus of irradiating biological specimens
    • 照射生物标本的装置
    • US5395591A
    • 1995-03-07
    • US999434
    • 1992-12-30
    • William C. Zimlich, Jr.Joseph A. Sorge
    • William C. Zimlich, Jr.Joseph A. Sorge
    • C07K17/00C12Q1/68G05D25/02
    • C07K17/00C12Q1/68Y10T436/25
    • A method of irradiating a biological specimen with ultraviolet, in particular a polynucleotide specimen selected from DNA or RNA, or optionally a protein. In the case where the specimen is DNA or RNA, or potentially proteins, the specimen is irradiated to cross-link the specimen to a substrate. In the case where the specimen is DNA, the specimen can also be irradiated to form thymine dimers. The method uses an apparatus which permits relatively precise control of the total ultraviolet dose received by the specimen, despite any changes of ultraviolet flux from the lamps which may occur from during any one experiment, or between a number of experiments. Thus, the method allows relatively highly reproducible results to be obtained.
    • 用紫外线照射生物样本的方法,特别是选自DNA或RNA的多核苷酸标本,或任选的蛋白质。 在标本是DNA或RNA或潜在的蛋白质的情况下,照射样品以将样品交联到基底上。 在标本为DNA的情况下,也可以照射样品以形成胸腺嘧啶二聚体。 该方法使用允许相对精确地控制由样品接收的总紫外线剂量的装置,尽管在任何一个实验期间或在多个实验之间可能发生来自灯的紫外线通量的任何变化。 因此,该方法允许获得相对高度可重复的结果。
    • 4. 发明授权
    • Methods of enriching for and identifying polymorphisms
    • 富集和鉴定多态性的方法
    • US08383343B2
    • 2013-02-26
    • US10391090
    • 2003-03-18
    • Joseph A. Sorge
    • Joseph A. Sorge
    • C12Q1/68
    • C12N15/1072C12Q1/6827C12Q1/6869C12Q2565/519C12Q2565/531C12Q2533/101C12Q2522/101
    • The invention encompasses methods for enriching for and identifying a polymorphism within a nucleic acid sample either by separating a subset of a nucleic acid sample or by selectively replicating a subset of a nucleic acid sample such that the polymorphism is contained within a nucleic acid population with reduced complexity, and then identifying the polymorphism within the enriched nucleic acid sample. Methods also are disclosed for enriching for and identifying a polymorphism by contacting a nucleic acid sample that includes a subset of nucleic acid molecules having a sequence that binds to a sequence-specific binding activity with a molecule having a sequence-specific binding activity under conditions which permit specific binding, such that the subset of nucleic acid molecules bound to the activity is enriched for nucleic acid molecules having the sequence recognized by the sequence-specific binding activity, and detecting a polymorphism with respect to a reference sequence in the subset of nucleic acid molecules.
    • 本发明包括用于通过分离核酸样品的子集或通过选择性复制核酸样品的子集来使得核酸样品中的多态性富集和鉴定核酸样品中的多态性的方法,使得多态性包含在具有降低的核酸群体的核酸群体内 复杂性,然后鉴定富集的核酸样品内的多态性。 公开了通过使包含具有与序列特异性结合活性结合的序列的核酸分子的子集与具有序列特异性结合活性的分子的核酸样品接触的方法来丰富和鉴定多态性的方法, 允许特异性结合,使得与活性结合的核酸分子的子集富含具有由序列特异性结合活性识别的序列的核酸分子,并且检测核酸子集中的参考序列的多态性 分子。
    • 6. 发明申请
    • METHODS OF ENRICHING FOR AND IDENTIFYING POLYMORPHISMS
    • 增强和鉴别多态性的方法
    • US20100248246A1
    • 2010-09-30
    • US12749070
    • 2010-03-29
    • Joseph A. SorgeRonald W. Davis
    • Joseph A. SorgeRonald W. Davis
    • C12Q1/68
    • C12N15/1072C12Q1/6827C12Q1/6869C12Q2565/519C12Q2565/531C12Q2533/101C12Q2522/101
    • The invention encompasses methods for enriching for and identifying a polymorphism within a nucleic acid sample either by separating a subset of a nucleic acid sample or by selectively replicating a subset of a nucleic acid sample such that the polymorphism is contained within a nucleic acid population with reduced complexity, and then identifying the polymorphism within the enriched nucleic acid sample. Methods also are disclosed for enriching for and identifying a polymorphism by contacting a nucleic acid sample that includes a subset of nucleic acid molecules having a sequence that binds to a sequence-specific binding activity with a molecule having a sequence-specific binding activity under conditions which permit specific binding, such that the subset of nucleic acid molecules bound to the activity is enriched for nucleic acid molecules having the sequence recognized by the sequence-specific binding activity, and detecting a polymorphism with respect to a reference sequence in the subset of nucleic acid molecules.
    • 本发明包括用于通过分离核酸样品的子集或通过选择性复制核酸样品的子集来使得核酸样品中的多态性富集和鉴定核酸样品中的多态性的方法,使得多态性包含在具有降低的核酸群体的核酸群体内 复杂性,然后鉴定富集的核酸样品内的多态性。 公开了通过使包含具有与序列特异性结合活性结合的序列的核酸分子的子集与具有序列特异性结合活性的分子的核酸样品接触的方法来丰富和鉴定多态性的方法, 允许特异性结合,使得与活性结合的核酸分子的子集富含具有由序列特异性结合活性识别的序列的核酸分子,并且检测核酸子集中的参考序列的多态性 分子。
    • 9. 发明授权
    • Methods for detection of a target nucleic acid by capture
    • 通过捕获检测靶核酸的方法
    • US07361467B2
    • 2008-04-22
    • US11150775
    • 2005-06-10
    • Joseph A. SorgeAnne M. Whalen
    • Joseph A. SorgeAnne M. Whalen
    • C12Q1/68C12P19/34C07H21/02C07H21/04
    • C12Q1/6823C12Q1/6816C12Q2521/301C12Q2531/113C12Q2521/307C12Q2525/161C12Q2525/301C12Q2561/109C12Q2565/519C12Q2561/101C12Q2521/107
    • The invention relates to a method of generating a signal indicative of the presence of a target nucleic acid in a sample, where the method includes forming a cleavage structure by incubating a sample comprising a target nucleic acid with a probe having a secondary structure that changes upon binding of the probe to the target nucleic acid and further comprising a binding moiety. The invention also includes the steps of cleaving the cleavage structure with a nuclease to release a nucleic acid fragment to generate a signal, wherein generation of the signal is indicative of the presence of a target nucleic acid in a sample, and detecting and/or measuring the amount of the fragment captured by binding of a binding moiety to a capture element on a solid support.The invention also relates to a method of detecting or measuring a target nucleic acid in a sample, where the method includes forming a cleavage structure by incubating a sample containing a target nucleic acid with a probe having a secondary structure that changes upon binding of the probe to a target nucleic acid and comprising a binding moiety, and cleaving the cleavage structure with a nuclease to generate a cleaved nucleic acid fragment and detecting and/or measuring the amount of the fragment captured by binding of a binding moiety to a capture element on a solid support.
    • 本发明涉及产生指示样品中目标核酸存在的信号的方法,其中该方法包括通过将包含靶核酸的样品与具有二级结构变化的探针一起孵育形成切割结构 探针与靶核酸的结合并且还包含结合部分。 本发明还包括用核酸酶切割切割结构以释放核酸片段以产生信号的步骤,其中产生信号指示样品中靶核酸的存在,以及检测和/或测量 通过结合部分与固体支持物上的捕获元件结合捕获的片段的量。 本发明还涉及一种检测或测量样品中的靶核酸的方法,其中该方法包括通过将含有靶核酸的样品与具有在探针结合后变化的二级结构的探针形成切割结构 并且包含结合部分,并用核酸酶切割切割结构以产生切割的核酸片段,并通过结合部分与捕获元件的结合捕获的片段的量,并检测和/或测量 坚实的支持。