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    • 6. 发明申请
    • METHODS FOR TESTING OF THERAPEUTIC COMPOUNDS
    • 治疗化合物检测方法
    • WO1996024693A1
    • 1996-08-15
    • PCT/SE1996000078
    • 1996-01-25
    • ASTRA AKTIEBOLAGKRISTOFFERSON, Ann
    • ASTRA AKTIEBOLAG
    • C12Q01/70
    • A61K49/0006
    • The present invention is related to a method for determining the efficacy of a chemical compound for treatment of recurrent herpes virus infection, said method comprising: (a) inoculating herpes virus at a primary skin site of a non-human mammal to cause zosteriform spread of the virus through nerve cells to cause lesions at a secondary (distal) site of infection; (b) before the appearance of skin lesions at the secondary site caused by the virus, giving adoptive transfer of immunity (ATI) to the said non-human mammal, so as to provide immunity mimicking the immunological reactivity seen in a recurrent herpes virus infection in a previously infected immune host; (c) administering a chemical compound to be tested to the said non-human mammal; and (d) determining the ability of the said chemical compound to reduce the occurrence and/or severity of herpes virus-induced skin lesions at the secondary site of infection.
    • 本发明涉及一种用于确定化合物治疗复发性疱疹病毒感染的功效的方法,所述方法包括:(a)在非人哺乳动物的原皮肤部位接种疱疹病毒以引起疱疹病毒感染 病毒通过神经细胞在继发(远端)感染部位引起病变; (b)在由病毒引起的次级部位出现皮肤损伤之前,对所述非人哺乳动物进行过继免疫转移(ATI),以提供模仿复发性疱疹病毒感染中所见的免疫反应的免疫力 在先前感染的免疫宿主中; (c)向所述非人哺乳动物施用待测化合物; 和(d)确定所述化合物减少感染次要部位的疱疹病毒诱导的皮肤损伤的发生和/或严重性的能力。
    • 7. 发明申请
    • USING LAMBDOID BACTERIOPHAGES LINKED BY OLIGONUCLEOTIDES TO SOLID SUPPORT
    • 使用由寡核苷酸连接的LABBDOID BACTERIOPAGES结合实际支持
    • WO1996021043A1
    • 1996-07-11
    • PCT/US1996000108
    • 1996-01-02
    • SYMBIOTECH, INC.
    • SYMBIOTECH, INC.RAY, Bryan, L.LIN, Edmund, C., C.
    • C12Q01/70
    • C12Q1/706A61K47/6901C07K14/005C12N7/00C12N2795/10321C12N2795/10322C12N2795/10345C12N2795/10362C12Q1/6823C12Q1/70C12Q1/707C12Q2521/301
    • The present invention provides compositions, methods and kits for detection and quantitation of pathogenic organisms. The composition of the invention is an oligonucleotide probe comprising a bacteriophage covalently linked to one site on an oligonucleotide probe complementary to a conserved region of a pathogenic organism. At a second site, the oligonucleotide probe is linked to a matrix. The oligonucleotide probe contains a region complementary to one strand of a restriction endonuclease recognition site or an oligoribonucleotide moiety. The number of pathogenic organisms present in a biological fluid sample may be quantitated in accordance with the method of the invention by combining the composition of the invention with the sample, allowing hybridization to occur. Hybridization generates the intact restriction endonuclease site or a DNA-RNA hybrid, and by adding the appropriate restriction endonuclease or a nucleolytic enzyme capable of cleaving DNA-RNA hybrids, bacteriophage will be released for measurement. The kit of the invention provides components which allow the method of the invention to be performed.
    • 本发明提供了用于病原生物体的检测和定量的组合物,方法和试剂盒。 本发明的组合物是一种寡核苷酸探针,其包含与与致病生物体的保守区域互补的寡核苷酸探针上的一个位点共价连接的噬菌体。 在第二个位点,寡核苷酸探针与基质连接。 寡核苷酸探针含有与限制性内切核酸酶识别位点的一条链或寡核糖核苷酸部分互补的区域。 存在于生物流体样品中的致病生物体的数量可以根据本发明的方法通过将本发明的组合物与样品组合进行定量,从而进行杂交。 杂交产生完整的限制性内切酶位点或DNA-RNA杂交体,通过加入适当的限制性内切核酸酶或能够切割DNA-RNA杂交体的核解质酶,噬菌体将被释放用于测量。 本发明的试剂盒提供允许本发明方法进行的组分。
    • 10. 发明申请
    • METHOD OF DETECTING CELLULAR MATERIAL
    • 检测细胞材料的方法
    • WO1995034685A1
    • 1995-12-21
    • PCT/US1995007466
    • 1995-06-13
    • GENZYME CORPORATION
    • GENZYME CORPORATIONMAHR, Anna, M.BOWE, Ann, E.RUFF-ROBERTS, Alyson, L.KLINGER, Katherine, W.
    • C12Q01/70
    • C12Q1/6806C12Q1/6841
    • The method of the present invention relates to a rapid procedure for detecting DNA in a cell, while preserving the morphology of the nucleus for analysis. The method comprises depositing a cell onto a polymeric membrane filter wherein the DNA contained in the cell is retained on the polymeric membrane filter and is available for binding with a fluorescently labeled nucleic acid probe, incubating the polymeric membrane filter with the labeled nucleic acid probe, and detecting the labeled nucleic acid probe wherein detection of the nucleic acid probe is indicative of the presence of the DNA. There are no separate permeabilization steps needed to permit the probes to enter the cell and hybridize to the DNA. The method is simple and quick and is applicable to the sample volumes found in clinical laboratories. The method of the present invention allows for analysis with single copy sequence probes of cells sorted onto, filtered onto, grown on or settled onto polymeric membrane filters. In addition, the method allows for the hybridization of probes containing single copy or repetitive DNA sequences to metaphase chromosomes as well as to interphase nuclei on membrane filters.
    • 本发明的方法涉及用于检测细胞中DNA的快速方法,同时保留用于分析的细胞核的形态。 该方法包括将细胞沉积在聚合物膜过滤器上,其中包含在细胞中的DNA保留在聚合物膜过滤器上,并且可用于与荧光标记的核酸探针结合,将聚合物膜过滤器与标记的核酸探针, 并检测标记的核酸探针,其中核酸探针的检测指示DNA的存在。 不需要单独的透化步骤来允许探针进入细胞并与DNA杂交。 该方法简便快捷,适用于临床实验室的样品量。 本发明的方法允许用分选到,过滤到,生长在或沉积在聚合物膜过滤器上的细胞的单拷贝序列探针进行分析。 此外,该方法允许将含有单拷贝或重复DNA序列的探针杂交到中期染色体以及膜过滤器上的间期核。