摘要:
Disclosed is a method for controlling the microbiological quality of an environmental aqueous medium, suspected of containing various micro-organisms, having the following steps: selecting a reference set, having at least three micro-organisms, representing jointly or separately a microbiological quality level; providing a microbiological detection kit, having at least three probes specifically and respectively identifying said three micro-organisms; after treating the medium to be analyzed, contacting said micro-organisms, or any fraction thereof derived from the medium to be analyzed therefrom, with said detection kit, whereby a multiple determination of the micro-organisms is carried out, the determination representing the microbiological quality level of the medium.
摘要:
The present invention relates to a method for neuroblastoma prognosis in a patient suffering from neuroblastoma, characterized in that it comprises the following steps: a. biological material is extracted from a biological sample taken from the patient, b. the biological material is brought into contact with at least one specific reagent chosen from the reagents specific for the target genes exhibiting a nucleic acid sequence having any one of SEQ ID Nos. 1 to 37, it being understood that, when the target gene exhibits a nucleic acid sequence having one of SEQ ID Nos. 11, 17 or 37, the biological material is brought into contact with at least two specific reagents chosen from the reagents specific for the target genes exhibiting a nucleic acid sequence having any one of SEQ ID Nos. 1 to 37, c. the expression of at least one of said target genes is determined, it being understood that, when the target gene exhibits a nucleic acid sequence having one of SEQ ID Nos. 11, 17 or 37, the expression of at least two of said target genes is determined.
摘要翻译:本发明涉及神经母细胞瘤患者神经母细胞瘤预后的方法,其特征在于包括以下步骤:a。 生物材料从取自患者的生物样品中提取,b。 使生物材料与选自对具有SEQ ID No.1至37中任一项所示的核酸序列的靶基因特异性的试剂中的至少一种特异性试剂接触,应理解,当靶基因表现出 具有SEQ ID No.11,17或37之一的核酸序列,使生物材料与至少两种特异性试剂接触,所述试剂选自对具有SEQ ID NO:11,17或37中任一项所示的核酸序列的靶基因特异性的试剂 1至37,c。 确定至少一个所述靶基因的表达,应当理解,当靶基因表现出具有SEQ ID No.11,17或37之一的核酸序列时,至少两个所述靶基因的表达 决心,决意,决定。
摘要:
The sequences of 5′ ESTs derived from mRNAs encoding secreted proteins are disclosed. The 5′ ESTs may be to obtain cDNAs and genomic DNAs corresponding to the 5′ ESTs. The 5′ ESTs may also be used in diagnostic, forensic, gene therapy, and chromosome mapping procedures. Upstream regulatory sequences may also be otained using the 5′ ESTs. The 5′ ESTs may also be used to design expression vectors and secretion vectors.
摘要:
The present invention relates to a method for detecting and/or identifying bacteria of the genus Staphylococcus, comprising the following steps: A. the nucleic acid material of the bacteria of the genus Staphylococcus is extracted, B. at least one target sequence of the nucleic acid material of the bacteria of the genus Staphylococcus is amplified using at least one amplification primer comprising at least 10 nucleotide motifs of SEQ ID No. 1 and/or at least one amplification primer comprising at least 10 nucleotide motifs of SEQ ID No. 2, in order to obtain amplicons of the target sequence, C. the presence of bacteria of the genus Staphylococcus is determined by detecting said amplicons.
摘要翻译:本发明涉及一种用于检测和/或鉴定葡萄球菌属细菌的方法,包括以下步骤:A.提取葡萄球菌属细菌的核酸物质,B.核酸的至少一个靶序列 使用至少一个包含SEQ ID No.1的至少10个核苷酸基序的扩增引物和/或至少一个包含SEQ ID No.2的至少10个核苷酸基序的扩增引物扩增葡萄球菌属细菌的酸性物质, 以获得靶序列的扩增子,C.通过检测所述扩增子来确定葡萄球菌属细菌的存在。
摘要:
The present invention relates to a method for detecting and/or identifying bacteria of the genus Staphylococcus, comprising the following steps: A. the nucleic acid material of the bacteria of the genus Staphylococcus is extracted, B. at least one target sequence of the nucleic acid material of the bacteria of the genus Staphylococcus is amplified using at least one amplification primer comprising at least 10 nucleotide motifs of SEQ ID No. 1 and/or at least one amplification primer comprising at least 10 nucleotide motifs of SEQ ID No. 2, in order to obtain amplicons of the target sequence, C. the presence of bacteria of the genus Staphylococcus is determined by detecting said amplicons.
摘要翻译:本发明涉及一种用于检测和/或鉴定葡萄球菌属细菌的方法,包括以下步骤:A.提取葡萄球菌属细菌的核酸物质,B.核酸的至少一个靶序列 使用至少一个包含SEQ ID No.1的至少10个核苷酸基序的扩增引物和/或至少一个包含SEQ ID No.2的至少10个核苷酸基序的扩增引物扩增葡萄球菌属细菌的酸性物质, 以获得靶序列的扩增子,C.通过检测所述扩增子来确定葡萄球菌属细菌的存在。
摘要:
Disclosed is a method for detecting or identifying the original animal species in a sample likely to contain an ingredient obtained at least from said species. The inventive method is characterized by the following steps: a) a nuclear fraction is obtained from said sample; b) at least one reactant which is specific to the animal species is provided and selected among a group formed by: - the reference sequences SEQ ID numbers 1 to 232, 242 to 261; - the sequences complementing each of the sequences SED ID numbers 1 to 232, 242 to 261, respectively; - the sequences homologous to each of the sequences SEQ ID numbers 1 to 232, 242 to 261 and sequences complementing each of the sequences SED ID numbers 1 to 232, 242 to 261, respectively; c) the nuclear fraction and said reactant are reacted with each other; and d) any signal or information resulting from the specific reaction between said reactant and the nuclear fraction is detected, whereby it can be established if said sample contains said original animal species.
摘要:
The sequences of 5′ ESTs derived from mRNAs encoding secreted proteins are disclosed. The 5′ ESTs may be to obtain cDNAs and genomic DNAs corresponding to the 5′ ESTs. The 5′ ESTs may also be used in diagnostic, forensic, gene therapy, and chromosome mapping procedures. Upstream regulatory sequences may also be obtained using the 5′ ESTs. The 5′ ESTs may also be used to design expression vectors and secretion vectors.
摘要:
Materials and methods for identifying unique sites in bacterial 16S and 23S rDNA are provided, as well as specific unique sequences of 16S rDNA in select bacteria. The distinguishing moieties will enable rapid differentiation between families, genera, groups, species, strains, subspecies, and isolates of microorganisms. Such differentiation can be performed by using rapid screening kits in combination with in silico analysis for diagnostic, prognastic, epidemiologic, phylogenetic, and other purposes.
摘要:
The sequences of 5′ ESTs derived from mRNAs encoding secreted proteins are disclosed. The 5′ ESTs may be to obtain cDNAs and genomic DNAs corresponding to the 5′ ESTs. The 5′ ESTs may also be used in diagnostic, forensic, gene therapy, and chromosome mapping procedures. Upstream regulatory sequences may also be otained using the 5′ ESTs. The 5′ ESTs may also be used to design expression vectors and secretion vectors.