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    • 2. 发明申请
    • SALMONELLA DETECTION ASSAY
    • SALMONELLA检测测定
    • WO2009147435A1
    • 2009-12-10
    • PCT/GB2009/050617
    • 2009-06-03
    • HEALTH PROTECTION AGENCYHOPKINS, KatieLAWSON, Andy
    • HOPKINS, KatieLAWSON, Andy
    • C12Q1/68
    • C12Q1/689C12Q2600/166Y02A50/451
    • There is provided a method and reagents for detecting S. enterica subsp . IIIa and/ or IIIb in a sample, the method comprising: (a) contacting the sample with a pair of forward and reverse oligonucleotide primers, wherein said forward and reverse primers hybridise to target nucleic acid sequences located within the lacZ gene of S. enterica subsp . Ill, or the complement thereof; (b) extending said forward and reverse primers to generate an amplification product; and (c) detecting the amplification product. There is also provided a method a reagents for detecting S. enterica subsp . I in a sample, the method comprising: (a) contacting the sample with a pair of forward and reverse oligonucleotide primers, wherein said forward and reverse primers hybridise to target nucleic acid sequences located within the hilA gene of S. enterica subsp. I, or the complement thereof; (b) extending said forward and reverse primers to generate an amplification product; and (c) detecting the amplification product.
    • 提供了一种用于检测肠杆菌亚种的方法和试剂。 IIIa和/或IIIb的方法,所述方法包括:(a)使样品与一对正向和反向寡核苷酸引物接触,其中所述正向和反向引物与位于肠杆菌lacZ基因内的靶核酸序列杂交 亚种。 或其补体; (b)扩展所述正向和反向引物以产生扩增产物; 和(c)检测扩增产物。 还提供了一种用于检测肠炎沙门氏菌的试剂的方法。 I的方法包括:(a)使样品与一对正向和反向寡核苷酸引物接触,其中所述正向引物和反向引物与位于肠炎沙门氏菌的hILA基因内的靶核酸序列杂交。 I或其补体; (b)扩展所述正向和反向引物以产生扩增产物; 和(c)检测扩增产物。
    • 8. 发明申请
    • CLOSTRIDIUM DIFFICILE ANTIGENS
    • 胶原蛋白抗体
    • WO2012046061A2
    • 2012-04-12
    • PCT/GB2011/051910
    • 2011-10-05
    • HEALTH PROTECTION AGENCYMICROPHARM LIMITEDSHONE, CliffordROBERTS, AprilAHERN, HelenMAYNARD-SMITH, MichaelLANDON, John
    • SHONE, CliffordROBERTS, AprilAHERN, HelenMAYNARD-SMITH, MichaelLANDON, John
    • C07K14/435
    • A61K39/08A61K38/164A61K39/40A61K2039/505C07K14/33C07K16/1282C07K2317/76C07K2319/00
    • The present invention relates to recombinant Clostridium difficile antigens based on a fusion protein that consists of or comprises a first amino acid sequence and a second amino acid sequence, wherein: a) the first amino acid sequence is provided by an amino acid sequence that has at least 80% sequence identity with an amino acid sequence consisting of residues 500-1850 of a C. difficile Toxin A sequence or residues 1500-1851 of a C. difficile Toxin B sequence; and b) the second amino acid sequence is provided by an amino acid sequence that has at least 80% sequence identity with an amino acid sequence consisting of a long repeat unit located within amino acid residues 1851-2710 of a C. difficile Toxin A sequence or within amino acid residues 1852-2366 of a C. difficile Toxin B sequence; though with the proviso that the fusion protein is not a polypeptide comprising amino acid residues 543-2710 of a C. difficile Toxin A and with the proviso that the fusion protein is not a polypeptide comprising amino acid residues 543-2366 of a C. difficile Toxin B. Also provided is the use of said antigens for the prevention/ treatment/ suppression of Clostridium difficile infection (CDI), together with methods for generating said antigens, methods for generating antibodies that bind to said antigens, and the use of said antibodies for the prevention/ treatment/ suppression of CDI.
    • 本发明涉及基于由第一氨基酸序列和第二氨基酸序列组成或包含第一氨基酸序列和第二氨基酸序列的融合蛋白的重组艰难梭菌抗原,其中:a)第一个氨基酸序列由具有 与艰难梭菌毒素A序列的残基500-1850和艰难梭菌毒素B序列的残基1500-1851组成的氨基酸序列具有至少80%的序列同一性; 和b)第二个氨基酸序列由氨基酸序列提供,该氨基酸序列与由位于艰难梭菌毒素A序列的氨基酸残基1851-2710内的长重复单元组成的氨基酸序列具有至少80%的序列同一性 或艰难梭菌毒素B序列的氨基酸残基1852-2366内; 尽管条件是融合蛋白不是包含艰难梭菌毒素A的氨基酸残基543-2710的多肽,条件是融合蛋白不是包含艰难梭菌的氨基酸残基543-2366的多肽 毒素B.还提供了所述抗原用于预防/治疗/抑制艰难梭菌感染(CDI)的用途,以及产生所述抗原的方法,产生结合所述抗原的抗体的方法和所述抗体的使用 用于预防/治疗/抑制CDI。