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    • 2. 发明授权
    • Process for typing of HCV isolates
    • HCV分离株的分型方法
    • US06495670B1
    • 2002-12-17
    • US09378900
    • 1999-08-23
    • Geert MaertensLieven StuyverRudi RossauHugo Van Heuverswyn
    • Geert MaertensLieven StuyverRudi RossauHugo Van Heuverswyn
    • C07H2102
    • C12Q1/707C12Q1/6834C12Q2563/131C12Q2545/101C12Q2525/101C12Q2531/113
    • The invention relates to a process for genotyping any HCV isolate present in a biological sample, previously identified as being HCV positive, and for classifying said isolate according to the percentage of homology with other HCV isolates, comprising the steps of: contacting said sample in which the ribonucleotides or deoxyribonucleotides have been made accessible, if need be, under suitable denaturation, with at least one probe from about 10 to about 40 nucleotides, with said probe being liable to hybridize to a region being in the domain extending from nucleotide at position −291 to nucleotide at position −66 of the 5′ untranslated region of one of the HCV isolates represented by their cDNA sequences, with said numbering of position beginning with the first ATG codon of the open reading frame encoding the HCV polyprotein, or with said probe being complementary to the above-defined probes, detecting the complexes possibly formed between said probe and the nucleotide sequence of the HCV isolate to be identified.
    • 本发明涉及用于对先前鉴定为HCV阳性的生物样品中存在的任何HCV分离物进行基因分型的方法,以及根据与其它HCV分离株的同源性百分比对所述分离物进行分类的方法,包括以下步骤: 如果需要的话,核糖核苷酸或脱氧核糖核苷酸可以在合适的变性下与至少一个约10至约40个核苷酸的探针接触,所述探针易于与位置延伸的结构域延伸的区域杂交。 291到由其cDNA序列表示的HCV分离物之一的5'非翻译区的-66位的核苷酸,其中所述编号的位置开始于编码HCV多蛋白的开放阅读框的第一个ATG密码子,或与所述探针 与上述定义的探针互补,检测可能形成于所述探针和HCV核苷酸序列之间的复合物 分离鉴定。
    • 3. 发明申请
    • Process for typing of HCV isolates
    • HCV分离株的分型方法
    • US20100120121A1
    • 2010-05-13
    • US11826099
    • 2007-07-12
    • Geert MaertensLieven StuyverRudi RossauHugo Van Heuverswyn
    • Geert MaertensLieven StuyverRudi RossauHugo Van Heuverswyn
    • C12N7/01C07H21/00
    • C12Q1/707
    • The invention relates to a process for genotyping any HCV isolate present in a biological sample, previously identified as being HCV positive, and for classifying said isolate according to the percentage of homology with other HCV isolates, comprising the steps of: contacting said sample in which the ribonucleotides or deoxyribonucleotides have been made accessible, if need be, under suitable denaturation, with at least one probe from about 10 to about 40 nucleotides, with said probe being liable to hybridize to a region being in the domain extending from nucleotide at position −291 to nucleotide at position −66 of the 5′ untranslated region of one of the HCV isolates represented by their cDNA sequences, with said numbering of position beginning with the first ATG codon of the open reading frame encoding the HCV polyprotein, or with said probe being complementary to the above-defined probes, detecting the complexes possibly formed between said probe and the nucleotide sequence of the HCV isolate to be identified.
    • 本发明涉及用于对先前鉴定为HCV阳性的生物样品中存在的任何HCV分离物进行基因分型的方法,以及根据与其它HCV分离株的同源性百分比对所述分离物进行分类的方法,包括以下步骤: 如果需要的话,核糖核苷酸或脱氧核糖核苷酸可以在合适的变性下与至少一个约10至约40个核苷酸的探针接触,所述探针易于与位置延伸的结构域延伸的区域杂交。 291到由其cDNA序列表示的HCV分离物之一的5'非翻译区的-66位的核苷酸,其中所述编号的位置开始于编码HCV多蛋白的开放阅读框的第一个ATG密码子,或与所述探针 与上述探针互补,检测可能在所述探针和核苷酸序列之间形成的复合物 HCV分离株被鉴定。
    • 6. 发明授权
    • Process for typing of HCV isolates
    • HCV分离株的分型方法
    • US07258982B2
    • 2007-08-21
    • US10822711
    • 2004-04-13
    • Geert MaertensLieven StuyverRudi RossauHugo Van Heuverswyn
    • Geert MaertensLieven StuyverRudi RossauHugo Van Heuverswyn
    • C12Q1/68C07H21/02C07H21/04
    • C12Q1/707C12Q1/6834C12Q2563/131C12Q2545/101C12Q2525/101C12Q2531/113
    • The invention relates to a process for genotyping any HCV isolate present in a biological sample, previously identified as being HCV positive, and for classifying said isolate according to the percentage of homology with other HCV isolates, comprising the steps of: contacting said sample in which the ribonucleotides or deoxyribonucleotides have been made accessible, if need be, under suitable denaturation, with at least one probe from about 10 to about 40 nucleotides, with said probe being liable to hybridize to a region being in the domain extending from nucleotide at position −291 to nucleotide at position −66 of the 5′ untranslated region of one of the HCV isolates represented by their cDNA sequences, with said numbering of position beginning with the first ATG codon of the open reading frame encoding the HCV polyprotein, or with said probe being complementary to the above-defined probes, detecting the complexes possibly formed between said probe and the nucleotide sequence of the HCV isolate to be identified.
    • 本发明涉及用于对先前鉴定为HCV阳性的生物样品中存在的任何HCV分离物进行基因分型的方法,以及根据与其它HCV分离株的同源性百分比对所述分离物进行分类的方法,包括以下步骤: 如果需要的话,核糖核苷酸或脱氧核糖核苷酸可以在合适的变性下与至少一个约10至约40个核苷酸的探针接触,所述探针易于与位置延伸的结构域延伸的区域杂交。 291到由其cDNA序列表示的HCV分离物之一的5'非翻译区的-66位的核苷酸,其中所述编号的位置开始于编码HCV多蛋白的开放阅读框的第一个ATG密码子,或与所述探针 与上述定义的探针互补,检测可能形成在所述探针与H的核苷酸序列之间的复合物 CV分离鉴定。
    • 8. 发明授权
    • Process for typing of HCV isolates
    • HCV分离株的分型方法
    • US6051696A
    • 2000-04-18
    • US44665
    • 1998-03-19
    • Geert MaertensLieven StuyverRudi RossauHugo Van Heuverswyn
    • Geert MaertensLieven StuyverRudi RossauHugo Van Heuverswyn
    • C12N15/09C07H21/04C12N15/40C12Q1/02C12Q1/68C12Q1/70C07H21/02C12N15/00
    • C12Q1/707C12Q1/6834
    • The invention relates to a process for genotyping any HCV isolate present in a biological sample, previously identified as being HCV positive, and for classifying said isolate according to the percentage of homology with other HCV isolates, comprising the steps of:contacting said sample in which the ribonucleotides or deoxyribonucleotides have been made accessible, if need be, under suitable denaturation, with at least one probe from about 10 to about 40 nucleotides, with said probe being liable to hybridize to a region being in the domain extending from nucleotide at position -291 to nucleotide at position -66 of the 5' untranslated region of one of the HCV isolates represented by their cDNA sequences, with said numbering of position beginning with the first ATG codon of the open reading frame encoding the HCV polyprotein, br with said probe being complementary to the above-defined probes,detecting the complexes possibly formed between said probe and the nucleotide sequence of the HCV isolate to be identified.
    • 本发明涉及用于对先前鉴定为HCV阳性的生物样品中存在的任何HCV分离物进行基因分型的方法,以及根据与其它HCV分离株的同源性百分比对所述分离物进行分类的方法,包括以下步骤: 如果需要的话,核糖核苷酸或脱氧核糖核苷酸可以在合适的变性下与至少一个约10至约40个核苷酸的探针接触,所述探针易于与位置延伸的结构域延伸的区域杂交。 291到由其cDNA序列表示的HCV分离物之一的5'非翻译区的-66位的核苷酸,所述编号的位置以编码HCV多聚蛋白的开放阅读框的第一个ATG密码子开始,所述探针 与上述定义的探针互补,检测可能形成在所述探针与H的核苷酸序列之间的复合物 CV分离鉴定。