Optimized real time nucleic acid detection processes
    51.
    发明授权
    Optimized real time nucleic acid detection processes 有权
    优化的实时核酸检测过程

    公开(公告)号:US09353405B2

    公开(公告)日:2016-05-31

    申请号:US13436174

    申请日:2012-03-30

    IPC分类号: C12Q1/68 C12Q1/70

    摘要: This invention provides for compositions for use in real time nucleic acid detection processes. Such real time nucleic acid detection processes are carried out with energy transfer elements attached to nucleic acid primers, nucleotides, nucleic acid probes or nucleic acid binding agents. Real time nucleic acid detection allows for the qualitative or quantitative detection or determination of single-stranded or double-stranded nucleic acids of interest in a sample. Other processes are provided by this invention including processes for removing a portion of a homopolymeric sequence, e.g., poly A sequence or tail, from an analyte or library of analytes. Compositions useful in carrying out such removal processes are also described and provided. Paneling and multiplex analyzes of more than one nucleic acid analyte using one sample are also provided.

    摘要翻译: 本发明提供用于实时核酸检测过程的组合物。 这种实时核酸检测方法是用连接于核酸引物,核苷酸,核酸探针或核酸结合剂的能量转移元件进行的。 实时核酸检测允许定性或定量检测或测定样品中感兴趣的单链或双链核酸。 本发明提供了其它方法,包括从被分析物或分析物库中除去一部分均聚物序列,例如聚A序列或尾部的方法。 还描述和提供了用于进行这种去除方法的组合物。 还提供了使用一个样品的多于一种核酸分析物的镶板和多重分析。

    Kits for amplifying and detecting nucleic acid sequences
    56.
    发明授权
    Kits for amplifying and detecting nucleic acid sequences 有权
    用于扩增和检测核酸序列的试剂盒

    公开(公告)号:US08445664B2

    公开(公告)日:2013-05-21

    申请号:US11256592

    申请日:2005-10-20

    IPC分类号: C07H21/04

    摘要: This invention provides novel processes for amplifying nucleic acid sequences of interest, including linear and non-linear amplification. In linear amplification, a single initial primer or nucleic acid construct is utilized to carry out the amplification process. In non-linear amplification, a first initial primer or nucleic acid construct is employed with a subsequent initial primer or nucleic acid construct. In other non-linear amplification processes provided by this invention, a first initial primer or nucleic acid construct is deployed with a second initial primer or nucleic acid construct to amplify the specific nucleic acid sequence of interest and its complement that are provided. A singular primer or a singular nucleic acid construct capable of non-linear amplification can also be used to carry out non-linear amplification in accordance with this invention. Post-termination labeling process for nucleic acid sequencing is also disclosed in this invention that is based upon the detection of tagged molecules that are covalently bound to chemically reactive groups provided for chain terminators. A process for producing nucleic acid sequences having decreased thermodynamic stability to complementary sequences is also provided and achieved by this invention. Unique nucleic acid polymers are also disclosed and provided in addition to other novel compositions, kits and the like.

    摘要翻译: 本发明提供用于扩增感兴趣的核酸序列的新方法,包括线性和非线性扩增。 在线性扩增中,使用单个初始引物或核酸构建体进行扩增过程。 在非线性扩增中,使用第一初始引物或核酸构建体与随后的初始引物或核酸构建体。 在本发明提供的其它非线性扩增方法中,用第二初始引物或核酸构建物展开第一个初始引物或核酸构建体,以扩增所提供的特异性核酸序列及其互补序列。 也可以使用能够进行非线性扩增的单一引物或单个核酸构建体来进行本发明的非线性扩增。 用于核酸测序的终止后标记方法也在本发明中公开,其基于共价结合到为链终止剂提供的化学反应性基团的标记分子的检测。 通过本发明提供并实现了对互补序列产生具有降低的热力学稳定性的核酸序列的方法。 除了其它新型组合物,试剂盒等之外,还公开并提供了独特的核酸聚合物。

    Processes for incorporating nucleic acid sequences into an analyte or library of analytes
    57.
    发明申请
    Processes for incorporating nucleic acid sequences into an analyte or library of analytes 有权
    将核酸序列并入分析物或分析物库中的方法

    公开(公告)号:US20060035264A1

    公开(公告)日:2006-02-16

    申请号:US11237466

    申请日:2005-09-27

    IPC分类号: C12Q1/68 C07H21/04

    摘要: This invention provides for compositions for use in real time nucleic acid detection processes. Such real time nucleic acid detection processes are carried out with energy transfer elements attached to nucleic acid primers, nucleotides, nucleic acid probes or nucleic acid binding agents. Real time nucleic acid detection allows for the qualitative or quantitative detection or determination of single-stranded or double-stranded nucleic acids of interest in a sample. Other processes are provided by this invention including processes for removing a portion of a homopolymeric sequence, e.g., poly A sequence or tail, from an analyte or library of analytes. Compositions useful in carrying out such removal processes are also described and provided.

    摘要翻译: 本发明提供用于实时核酸检测过程的组合物。 这种实时核酸检测方法是用连接于核酸引物,核苷酸,核酸探针或核酸结合剂的能量转移元件进行的。 实时核酸检测允许定性或定量检测或测定样品中感兴趣的单链或双链核酸。 本发明提供了其它方法,包括从被分析物或分析物库中除去一部分均聚物序列,例如聚A序列或尾部的方法。 还描述和提供了用于进行这种去除方法的组合物。

    Site- or sequence-specific process for cleaving analytes and library of analytes
    58.
    发明申请
    Site- or sequence-specific process for cleaving analytes and library of analytes 有权
    用于切割分析物和分析物库的位点或序列特异性方法

    公开(公告)号:US20060024738A1

    公开(公告)日:2006-02-02

    申请号:US11237467

    申请日:2005-09-27

    IPC分类号: C12Q1/68 C07H21/04

    摘要: This invention provides for compositions for use in real time nucleic acid detection processes. Such real time nucleic acid detection processes are carried out with energy transfer elements attached to nucleic acid primers, nucleotides, nucleic acid probes or nucleic acid binding agents. Real time nucleic acid detection allows for the qualitative or quantitative detection or determination of single-stranded or double-stranded nucleic acids of interest in a sample. Other processes are provided by this invention including processes for removing a portion of a homopolymeric sequence, e.g., poly A sequence or tail, from an analyte or library of analytes. Compositions useful in carrying out such removal processes are also described and provided.

    摘要翻译: 本发明提供用于实时核酸检测过程的组合物。 这种实时核酸检测方法是用连接于核酸引物,核苷酸,核酸探针或核酸结合剂的能量转移元件进行的。 实时核酸检测允许定性或定量检测或测定样品中感兴趣的单链或双链核酸。 本发明提供了其它方法,包括从被分析物或分析物库中除去一部分均聚物序列,例如聚A序列或尾部的方法。 还描述和提供了用于进行这种去除方法的组合物。

    Analyte detection utilizing polynucleotide sequences, composition, process and kit
    59.
    发明授权
    Analyte detection utilizing polynucleotide sequences, composition, process and kit 失效
    使用多核苷酸序列,组成,过程和试剂盒的分析物检测

    公开(公告)号:US09134302B2

    公开(公告)日:2015-09-15

    申请号:US08479995

    申请日:1995-06-07

    IPC分类号: C07H21/00 G01N33/53 C12Q1/68

    摘要: A method of detecting in a sample an analyte (A) having a molecularly recognizable portion thereon, which comprises: providing (B) a molecular bridging entity having thereon: (i) a portion capable of recognizing the molecularly recognizable portion on the analyte; and (ii) a portion comprising a polynucleotide sequence; and (C) a signalling entity having thereon: (i) a polynucleotide portion capable of annealing to the polynucleotide portion of the bridging entity, thereby to form a stable polynucleotide hybrid, and (ii) a signal generating portion; forming a complex comprising: (1) the analyte (A) complexed through its molecularly recognizable portion to (2) the recognizing portion of the entity (B); the entity (B) being complexed through the polynucleotide portion thereon to (3) the polynucleotide portion of the signalling entity; and detecting a signal by means of the signal generating portion present in the complex.

    摘要翻译: 在样品中检测其上具有分子可识别部分的分析物(A)的方法,其包括:提供(B)其上具有其上的分子桥接实体:(i)能够识别分析物上的分子识别部分的部分; 和(ii)包含多核苷酸序列的部分; 和(C)其上具有的信令实体:(i)能够退火到所述桥接实体的多核苷酸部分从而形成稳定的多核苷酸杂交体的多核苷酸部分,和(ii)信号产生部分; 形成复合物,其包括:(1)通过其分子可识别部分复合的分析物(A)至(2)实体(B)的识别部分; 实体(B)通过其上的多核苷酸部分复合到(3)信令实体的多核苷酸部分; 以及通过存在于复合体中的信号产生部分来检测信号。