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    • 2. 发明申请
    • SOLID PHASE SEQUENCING OF BIOPOLYMERS
    • 生物聚合物的固相序列
    • US20110172111A1
    • 2011-07-14
    • US12852336
    • 2010-08-06
    • Charles CantorHubert Köster
    • Charles CantorHubert Köster
    • C40B30/04
    • C12Q1/6872C12Q1/6874C12Q2565/501C12Q2531/113C12Q2521/525C12Q2565/627C12Q2531/119C12Q2523/301C12Q2531/137C12Q2521/301C12Q2531/149
    • This invention relates to methods for detecting and sequencing target nucleic acid sequences, to mass modified nucleic acid probes and arrays of probes useful in these methods, and to kits and systems which contain these probes. Useful methods involve hybridizing the nucleic acids or nucleic acids which represent complementary or homologous sequences of the target to an array of nucleic acid probes. These probes comprise a single-stranded portion, an optional double-stranded portion and a variable sequence within the single-stranded portion. The molecular weights of the hybridized nucleic acids of the set can be determined by mass spectroscopy, and the sequence of the target determined from the molecular weights of the fragments. Nucleic acids whose sequences can be determined include DNA or RNA in biological samples such as patient biopsies and environmental samples. Probes may be fixed to a solid support such as a hybridization chip to facilitate automated molecular weight analysis and identification of the target sequence.
    • 本发明涉及用于检测和测序靶核酸序列,批量修饰的核酸探针和可用于这些方法的探针阵列的方法,以及含有这些探针的试剂盒和系统。 有用的方法包括将代表靶的互补或同源序列的核酸或核酸与核酸探针阵列进行杂交。 这些探针包括在单链部分内的单链部分,任选的双链部分和可变序列。 该组的杂交核酸的分子量可以通过质谱法测定,并且靶标的序列由片段的分子量确定。 可以确定其序列的核酸包括生物样品中的DNA或RNA,例如患者活组织检查和环境样品。 探针可以固定在固体支持物例如杂交芯片上以促进自动化分子量分析和靶序列的鉴定。
    • 3. 发明申请
    • SELECTING NUCLEIC ACID SAMPLES SUITABLE FOR GENOTYPING
    • 选择适合基因的核酸样品
    • US20100285463A1
    • 2010-11-11
    • US12667135
    • 2008-06-27
    • Florian KronenbergVeit SchoenbornIris HeidAnita Brandstätter
    • Florian KronenbergVeit SchoenbornIris HeidAnita Brandstätter
    • C12Q1/68
    • C12Q1/6827C12Q2531/149C12Q2525/179
    • The present invention relates to a method for selecting a DNA sample comprising genomic DNA suitable for genotyping, comprising the steps of: i) pre-genotyping said genomic DNA using a set of polymorphic markers; ii) determining out of said set of polymorphic markers the percentage of polymorphic markers for which said genomic DNA is homozygous; and iii) selecting said DNA sample when said genomic DNA is homozygous for less than 70% of said set of polymorphic markers. Furthermore, a method of genotyping comprising a step of using a DNA sample selected by the method in accordance with the present invention and/or a step of applying the method provided herein is disclosed. The present invention also relates to a method for identifying a gene or a locus on a genome, said method comprising a step of using a DNA sample selected by the method provided herein and a step of applying the method described herein. Further, the present invention relates to a kit for carrying out the method in accordance with the present invention comprising primers for the amplification of the set of polymorphic markers employed herein.
    • 本发明涉及一种用于选择包含适合基因分型的基因组DNA的DNA样品的方法,其包括以下步骤:i)使用一组多态性标记对所述基因组DNA进行前基因分型; ii)确定所述多态性标记集合中所述基因组DNA是纯合的多态标志物的百分比; 以及iii)当所述基因组DNA对所述多态性标记物组的少于70%是纯合的时,选择所述DNA样品。 此外,公开了一种基因分型方法,其包括使用根据本发明的方法选择的DNA样品和/或应用本文提供的方法的步骤。 本发明还涉及用于鉴定基因组上的基因或基因座的方法,所述方法包括使用通过本文提供的方法选择的DNA样品的步骤和应用本文所述方法的步骤。 此外,本发明涉及用于实施根据本发明的方法的试剂盒,其包含用于扩增本文使用的多态性标记组的引物。
    • 5. 发明授权
    • Analyte-specific assays based on formation of a replicase substrate
    • 基于复制酶底物形成的分析物特异性测定
    • US06562575B1
    • 2003-05-13
    • US09891661
    • 2001-06-26
    • Gary A. Dahl
    • Gary A. Dahl
    • C12Q168
    • C12Q1/682C12Q2531/149
    • Methods and compositions are provided for assaying for a target analyte in a sample by formation of a substrate for a replicase. The target analyte, if present in the sample, is first bound to a reporter probe. The reporter probe comprises a first portion and a second portion. The first portion comprises a polynucleotide that encodes at least part of a sequence for an RNA that is a substrate for replication. The second portion comprises a molecule that has affinity for an analyte. The reporter probe itself is not a substrate for a replicase. However, a replicase substrate is generated by treating reporter probe which is bound to analyte with a composition having nuclease activity in order to release the parts of the first portion, and then the released parts and one or more mononucleotides or oligonucleotides comprising missing parts of the substrate sequence are joined with a composition having ligase activity. Newly formed substrate is replicated with a replicase, and a signal is measured which indicates the presence and quantity of analyte in the sample. The invention also provides methods and compositions for simultaneously assaying for any of multiple analytes in a sample.
    • 提供方法和组合物用于通过形成用于复制酶的底物来测定样品中的目标分析物。 目标分析物(如果存在于样品中)首先与报道探针结合。 记录探针包括第一部分和第二部分。 第一部分包含编码作为复制底物的RNA的序列的至少一部分的多核苷酸。 第二部分包含对分析物具有亲和性的分子。 报道探针本身不是复制酶的底物。 然而,通过用与具有核酸酶活性的组合物结合分析物的报道探针来释放复制酶底物以释放第一部分的部分,然后释放的部分和一个或多个单核苷酸或寡核苷酸包含缺失的部分 底物序列与具有连接酶活性的组合物连接。 用复制酶复制新形成的底物,并且测量指示样品中分析物的存在和量的信号。 本发明还提供用于同时测定样品中多种分析物中的任何一种的方法和组合物。
    • 9. 发明授权
    • Solid phase sequencing of biopolymers
    • 生物聚合物的固相测序
    • US08758995B2
    • 2014-06-24
    • US12852336
    • 2010-08-06
    • Charles R. CantorHubert Koster
    • Charles R. CantorHubert Koster
    • C12Q1/68C12P19/34C07H21/02C07H21/04
    • C12Q1/6872C12Q1/6874C12Q2565/501C12Q2531/113C12Q2521/525C12Q2565/627C12Q2531/119C12Q2523/301C12Q2531/137C12Q2521/301C12Q2531/149
    • This invention relates to methods for detecting and sequencing target nucleic acid sequences, to mass modified nucleic acid probes and arrays of probes useful in these methods, and to kits and systems which contain these probes. Useful methods involve hybridizing the nucleic acids or nucleic acids which represent complementary or homologous sequences of the target to an array of nucleic acid probes. These probes comprise a single-stranded portion, an optional double-stranded portion and a variable sequence within the single-stranded portion. The molecular weights of the hybridized nucleic acids of the set can be determined by mass spectroscopy, and the sequence of the target determined from the molecular weights of the fragments. Probes may be affixed to a solid support such as a hybridization chip to facilitate automated molecular weight analysis and identification of the target sequence.
    • 本发明涉及用于检测和测序靶核酸序列,批量修饰的核酸探针和可用于这些方法的探针阵列的方法,以及含有这些探针的试剂盒和系统。 有用的方法包括将代表靶的互补或同源序列的核酸或核酸与核酸探针阵列进行杂交。 这些探针包括在单链部分内的单链部分,任选的双链部分和可变序列。 该组的杂交核酸的分子量可以通过质谱法测定,并且靶标的序列由片段的分子量确定。 探针可以固定在诸如杂交芯片的固体支持物上,以便于自动化分子量分析和目标序列的鉴定。
    • 10. 发明授权
    • Solid phase sequencing of biopolymers
    • 生物聚合物的固相测序
    • US07803529B1
    • 2010-09-28
    • US09395409
    • 1999-09-14
    • Charles CantorHubert Köster
    • Charles CantorHubert Köster
    • C12Q1/68
    • C12Q1/6872C12Q1/6874C12Q2565/501C12Q2531/113C12Q2521/525C12Q2565/627C12Q2531/119C12Q2523/301C12Q2531/137C12Q2521/301C12Q2531/149
    • This invention relates to methods for detecting and sequencing target nucleic acid sequences, to mass modified nucleic acid probes and arrays of probes useful in these methods, and to kits and systems which contain these probes. Useful methods involve hybridizing the nucleic acids or nucleic acids which represent complementary or homologous sequences of the target to an array of nucleic acid probes. These probes comprise a single-stranded portion, an optional double-stranded portion and a variable sequence within the single-stranded portion. The molecular weights of the hybridized nucleic acids of the set can be determined by mass spectroscopy, and the sequence of the target determined from the molecular weights of the fragments. Nucleic acids whose sequences can be determined include DNA or RNA in biological samples such as patient biopsies and environmental samples. Probes may be fixed to a solid support such as a hybridization chip to facilitate automated molecular weight analysis and identification of the target sequence.
    • 本发明涉及用于检测和测序靶核酸序列,批量修饰的核酸探针和可用于这些方法的探针阵列的方法,以及含有这些探针的试剂盒和系统。 有用的方法包括将代表靶的互补或同源序列的核酸或核酸与核酸探针阵列进行杂交。 这些探针包括在单链部分内的单链部分,任选的双链部分和可变序列。 该组的杂交核酸的分子量可以通过质谱法测定,并且靶标的序列由片段的分子量确定。 可以确定其序列的核酸包括生物样品中的DNA或RNA,例如患者活组织检查和环境样品。 探针可以固定在固体支持物例如杂交芯片上以促进自动化分子量分析和靶序列的鉴定。