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    • 3. 发明申请
    • SIMULTANEOUS DETECTION, IDENTIFICATION AND DIFFERENTIATION OF EUBACTERIAL TAXA USING A HYBRIDIZATION ASSAY
    • 使用杂交测定法同时检测,鉴定和鉴定非特异性TAXA
    • WO1996000298A1
    • 1996-01-04
    • PCT/EP1995002452
    • 1995-06-23
    • INNOGENETICS N.V.JANNES, GeertROSSAU, RudiVAN HEUVERSWYN, Hugo
    • INNOGENETICS N.V.
    • C12Q01/68
    • C12Q1/689C12Q1/6888C12Q2600/16
    • The present invention relates to a method for detection and identification of at least one microorganism, or for the simultaneous detection of several microorganisms in a sample, comprising the steps of: (i) if need be releasing, isolating or concentrating the polynucleic acids present in the sample; (ii) if need be amplifying the 16S-23S rRNA spacer region, or a part of it, with at least one suitable primer pair; (iii) hybridizing the polynucleic acids of step (i) or (ii) with at least one and preferably more than one of the spacer probes as mentioned in table 1a or equivalents of thereof, under the appropriate hybridization and wash conditions, and/or with a taxon-specific probe derived from any of the spacer sequences as represented in figs. 1-103 under the same hybridization and wash conditions; (iv) detecting the hybrids formed in step (iii) with each of the probes used under appropriate hybridization and wash conditions; (v) identification of the microorganism(s) present in the sample from the differential hybridization signals obtained in step (iv).
    • 本发明涉及用于检测和鉴定至少一种微生物或同时检测样品中几种微生物的方法,包括以下步骤:(i)如果需要释放,分离或浓缩存在于 例子; (ii)如果需要用至少一个合适的引物对扩增16S-23S rRNA间隔区或其一部分; (iii)在合适的杂交和洗涤条件下,将步骤(i)或(ii)的多核酸与表1a或其等同物中所提及的至少一种并优选多于一种的间隔探针杂交,和/或 具有从图中所示的任何间隔序列衍生的分类群特异性探针。 1-103在相同的杂交和洗涤条件下; (iv)在适当的杂交和洗涤条件下使用每种探针检测在步骤(iii)中形成的杂交体; (v)从步骤(iv)中获得的差异杂交信号鉴定样品中存在的微生物。
    • 6. 发明申请
    • NOVEL PROCEDURE FOR OBTAINING PROTEINS STARTING FROM AN EXTRACT OF NON-COLLAGENOUS PROTEINS FROM BONY MATERIAL AND ITS USE FOR THE PREPARATION OF A NOVEL PROTEIN INHIBITING THE PROLIFERATION OF OSTEOBLASTS
    • 从蛋白质提取物中提取非蛋白质蛋白质的蛋白质的新方法及其用于制备新蛋白质抑制骨质疏松症的增殖
    • WO1991008749A1
    • 1991-06-27
    • PCT/EP1990002295
    • 1990-12-20
    • N.V. INNOGENETICS S.A.MAHY, PatrickVAN HEUVERSWYN, Hugo
    • N.V. INNOGENETICS S.A.
    • A61K35/32
    • C07K14/51C07K14/4703
    • The invention relates to a procedure for obtaining a protein purified to a satisfactory homogeneous state, starting from an extract of non-collagenous proteins of bone matrix. Another subject of the invention is a device for the implementation of the procedure of the invention, a protein inhibiting the proliferation of osteoblasts likely to be obtained by the above-mentioned procedure. The procedure described in the present invention is characterized in that it comprises the following steps: the extract of non-collagenous proteins, solubilized beforehand in a solvent, is subjected to a preparative chromatography in the liquid phase on a column of gel with the aid of an elution buffer and an electric field, under conditions such that the desired protein is eluted, and is found, during or at the end of the chromatography, to be present in solution in the elution buffer, alone and free from contaminants, in at least one of the fractions collected at the exit of the column, the fraction containing the desired protein in solution in the elution buffer is recovered, the elution buffer is removed and the desired protein is recovered which, if necessary, is subjected to a renaturation step and/or a reactivation step.
    • 本发明涉及从骨基质的非胶原性蛋白质的提取物开始获得纯化至令人满意的均匀状态的蛋白质的方法。 本发明的另一主题是用于实施本发明方法的装置,其是抑制可能通过上述方法获得的成骨细胞增殖的蛋白质。 本发明描述的方法的特征在于其包括以下步骤:预先在溶剂中增溶的非胶原蛋白的提取物在凝胶柱上经液相制备色谱,借助于 洗脱缓冲液和电场,在所需蛋白质被洗脱的条件下,并且在色谱法期间或结束时发现,至少存在于洗脱缓冲液的溶液中,单独且不含污染物 在塔的出口收集的级分之一,回收洗脱缓冲液中含有溶液中所需蛋白质的级分,除去洗脱缓冲液,回收所需的蛋白质,如果需要,其进行复性步骤和 /或重新激活步骤。
    • 8. 发明申请
    • PROCESS FOR TYPING OF HCV ISOLATES
    • 分离型HCV的方法
    • WO1994012670A2
    • 1994-06-09
    • PCT/EP1993003325
    • 1993-11-26
    • N.V. INNOGENETICS S.A.MAERTENS, GeertSTUYVER, LievenROSSAU, RudiVAN HEUVERSWYN, Hugo
    • N.V. INNOGENETICS S.A.
    • C12Q01/70
    • 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 与上述探针互补; 检测可能形成在所述探针和待鉴定的HCV分离物的核苷酸序列之间的复合物。