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    • 35. 发明申请
    • STIMULATED CELL STANDARDS
    • 刺激细胞标准
    • WO2010004336A2
    • 2010-01-14
    • PCT/GB2009/050815
    • 2009-07-09
    • HEALTH PROTECTION AGENCYSTEBBINGS, Richard John
    • STEBBINGS, Richard John
    • G01N33/96
    • G01N33/96
    • Methods for producing stimulated, positive and negative control reference standard for monitoring intracellular cytokine levels and cytokine release in test samples by stimulating cells to produce cytokines in the presence of a cytokine release inhibitor, fixing the stimulated cells with a fixative such as paraformaldehyde, washing to remove excess fixatives and freeze-drying the stimulated, fixed cells. Methods for producing labelled reference standards for cell proliferation assays are also disclosed, in which proliferation-competent mammalian cells, isolated from a human or animal body are labelled with a label, such as a dye, that is divided between daughter cells during cell proliferation (e.g. carboxyfluorescein succinimidyl ester), the cells are stimulated to proliferate, the proliferated cells are fixed by addition of a fixative and then preserved by freeze drying or cryopreservation.
    • 用于产生用于通过刺激细胞在细胞因子释放抑制剂存在下产生细胞因子的细胞内细胞因子水平和细胞因子释放来监测细胞内细胞因子水平和细胞因子释放的方法,用固定剂如多聚甲醛固定刺激的细胞,洗涤至 去除多余的固定剂并冷冻干燥受刺激的固定细胞。 还公开了用于产生细胞增殖测定的标记参考标准的方法,其中从人或动物体分离的增殖能力的哺乳动物细胞用细胞增殖期间在子细胞之间划分的标记(例如染料)进行标记( 例如羧基荧光素琥珀酰亚胺酯),刺激细胞增殖,通过加入固定剂固定增殖的细胞,然后通过冷冻干燥或冷冻保存来保存细胞。
    • 38. 发明申请
    • DETECTION OF HUMAN PAPILLOMAVIRUS
    • 人类斑马鱼的检测
    • WO2008096177A2
    • 2008-08-14
    • PCT/GB2008/050080
    • 2008-02-08
    • HEALTH PROTECTION AGENCYCORLESS, CarolineGUIVER, Malcolm
    • CORLESS, CarolineGUIVER, Malcolm
    • C12Q1/68
    • C12Q1/708
    • There is provided an in vitro method of detecting human papillomavirus nucleic acid in a sample, comprising: (a) contacting said sample with forward and reverse oligonucleotide primers, wherein said primers bind to target sites in the human papillomavirus L1 gene, or the complement thereof, under conditions suitable to promote amplification of a portion of said human papillomavirus L1 gene or complement, thereby generating an amplicon; (b) contacting said amplicon with a probe, wherein the probe binds to a target site within said amplicon; and (c) detecting binding of said probe to said amplicon; wherein said forward primer binds to a target site having the sequence SEQ ID NO: 1; and wherein said reverse primer binds to a target site having the sequence SEQ ID NO: 2.
    • 提供了一种在样品中检测人乳头瘤病毒核酸的体外方法,包括:(a)使所述样品与正向和反向寡核苷酸引物接触,其中所述引物结合人乳头瘤病毒L1基因或其补体中的靶位点 在适于促进部分所述人乳头瘤病毒L1基因或补体的扩增的条件下,从而产生扩增子; (b)使所述扩增子与探针接触,其中探针结合所述扩增子内的靶位点; 和(c)检测所述探针与所述扩增子的结合; 其中所述正向引物与具有序列SEQ ID NO:1的靶位点结合; 并且其中所述反向引物与具有序列SEQ ID NO:2的靶位点结合。