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    • 7. 发明公开
    • 요각류 유래의 비텔로제닌 단백질 및 이를 이용한 내분비교란물질 오염 측정하는 방법
    • 来自COPEPOD的VITELLGENIN蛋白质和使用该方法确定内切酶干扰素污染的方法
    • KR1020100015069A
    • 2010-02-12
    • KR1020080075971
    • 2008-08-04
    • 한양대학교 산학협력단
    • 이재성
    • C07K14/395C07K14/00
    • PURPOSE: A vitellogenin protein which is derived from Copepoda is provided to use as a biomarker for accurately measuring endocrine disruptor in marine ecosystem. CONSTITUTION: A vitellogenin protein is derived from Copepoda, Tigriopus japonicus. The vitellogenin has a sequence of sequence number 2. A polynucleotide encoding the vitellogenin has a sequence of sequence number 1. A composition for detecting endocrine disruptor contains an antibody which specifically binds to the vitellogenin. The antibody is monoclonal antibody. A method for measuring pollution by endocrine disruptor comprises: a step of measuring mRNA or protein expression of vitellogenin from a Copepoda sample; a step of comparing expression level of the sample with standard expression level from a unpolluted region; and a step of determining the degree of pollution of endocrine disruptor.
    • 目的:提供从桡足类衍生的卵黄蛋白原蛋白,用作准确测量海洋生态系统内分泌干扰物的生物标志物。 构成:卵黄蛋白原蛋白源自桡足蜱from属(Copepoda)。 卵黄发生素具有序列号2的序列。编码卵​​黄蛋白原的多核苷酸具有序列号1的序列。用于检测内分泌干扰物的组合物含有特异性结合卵黄发生素的抗体。 抗体是单克隆抗体。 用于测量内分泌干扰物污染的方法包括:从桡足类样品中测量卵黄发生素的mRNA或蛋白质表达的步骤; 将样品的表达水平与来自未污染区域的标准表达水平进行比较的步骤; 并确定内分泌干扰物的污染程度。
    • 9. 发明公开
    • 글리코겐 합성 개시제를 암호화하는 유전자 및 그의 용도
    • 基因编码GLYCOGEN合成引发剂及其用途
    • KR1020080021593A
    • 2008-03-07
    • KR1020077026195
    • 2007-02-21
    • 산토리 홀딩스 가부시키가이샤
    • 나카오요시히로고다마유키코시모나가도모코
    • C07K14/395
    • C07K14/395
    • The present invention relates to a gene encoding glycogen synthesis initiator and use thereof, in particular, a yeast for practical use with superior resistance property to dryness and/or low-temperature storage, alcoholic beverages produced with said yeast, and a method for producing said beverages. More particularly, the present invention relates to a yeast, whose resistance property to dryness and/or resistance property to low-temperature storage is enhanced by amplifying expression level of GLG1 or GLG2 gene encoding a Glg1p or Glg2p which is a glycogen synthesis initiator in brewer's yeast, especially non-ScGLG1 gene or non-ScGLG2 gene specific to a lager brewing yeast and to a method for producing alcoholic beverages with said yeast, etc. ® KIPO & WIPO 2008
    • 本发明涉及编码糖原合成引发剂的基因及其用途,特别是具有优异的耐干性和/或低温保存性的实际用途的酵母,所述酵母生产的酒精饮料及其制备方法 饮料。 更具体地说,本发明涉及通过扩增编码作为糖原合成引发剂的Glg1p或Glg2p的GLG1或GLG2基因的表达水平来提高其对低温储存的耐干燥性和/或抗性的抗性, 酵母,尤其是非ScGLG1基因或非高浓度酿造酵母特异性的非ScGLG2基因,以及用酵母等生产酒精饮料的方法。KIPO&WIPO 2008