Composition for Detecting Undifferentiated Human Pluripotent Stem Cell, Monoclonal Antibody 6-1 and Use Thereof
    42.
    发明申请
    Composition for Detecting Undifferentiated Human Pluripotent Stem Cell, Monoclonal Antibody 6-1 and Use Thereof 有权
    用于检测未分化的人多能干细胞,单克隆抗体6-1及其用途的组合物

    公开(公告)号:US20160097096A1

    公开(公告)日:2016-04-07

    申请号:US14806514

    申请日:2015-07-22

    Abstract: The present invention relates to a composition for detecting the undifferentiated human pluripotent stem cells comprising an agent useful for measuring the level of Desmoglein 2 (Dsg 2) mRNA or the protein thereof, a kit for detecting the undifferentiated human pluripotent stem cells comprising the said composition, a method for detecting the undifferentiated human pluripotent stem cells containing the step of measuring the level of Desmoglein 2 mRNA or the protein thereof, a method for evaluating the differentiation of human pluripotent stem cells and thereafter for separating the undifferentiated human pluripotent stem cells, a method for reducing the undifferentiated status of human pluripotent stem cells by inhibiting the expression or activation of Desmoglein 2, and a monoclonal antibody binding specifically to human Desmoglein 2.

    Abstract translation: 本发明涉及一种用于检测未分化的人多能干细胞的组合物,其包含可用于测定脱骨髓糖蛋白2(Dsg2)mRNA或其蛋白质的水平的试剂,用于检测未分化的人多能干细胞的试剂盒,所述试剂盒包含所述组合物 用于检测未分化的人多能干细胞的方法,所述方法包括测定脱骨髓蛋白素2 mRNA或其蛋白质的水平的步骤,评估人多能干细胞分化的方法,然后分离未分化的人多能干细胞, 通过抑制脱骨髓素蛋白2的表达或活化来减少人多能干细胞未分化状态的方法,以及特异性结合人骨髓蛋白2的单克隆抗体。

    Mutant Beta-Glucosidases Having Enhanced Activity and a Method for Producing Bioethanol Using the Same
    45.
    发明申请
    Mutant Beta-Glucosidases Having Enhanced Activity and a Method for Producing Bioethanol Using the Same 有权
    具有增强活性的突变型β-葡糖苷酶和使用其生产生物乙醇的方法

    公开(公告)号:US20150299733A1

    公开(公告)日:2015-10-22

    申请号:US14111721

    申请日:2012-04-13

    CPC classification number: C12P7/06 C12N9/2445 C12Y302/01021 Y02E50/17

    Abstract: The present invention relates to beta-glucosidase that is mutated to have enhanced activity, and a method for producing bioethanol using the same. More particularly, the present invention relates to a polynucleotide encoding beta-glucosidase that is mutated to have enhanced activity, beta-glucosidase expressed from the polynucleotide, an expression vector including the polynucleotide, a transformant that is transformed with the expression vector, a method for producing the mutated beta-glucosidase using the transformant, and a method for producing bioethanol using the transformant. The mutant beta-glucosidase of the present invention increases production of glucose much more than the conventional beta-glucosidase, and thus it can be widely used for economic production of bioethanol.

    Abstract translation: 本发明涉及突变以提高活性的β-葡糖苷酶,以及使用其生产生物乙醇的方法。 更具体地说,本发明涉及一种突变为具有增强活性的β-葡糖苷酶的多核苷酸,由多核苷酸表达的β-葡糖苷酶,包含多核苷酸的表达载体,用表达载体转化的转化体, 使用转化体产生突变的β-葡糖苷酶,以及使用转化体生产生物乙醇的方法。 本发明的突变型β-葡糖苷酶比常规的β-葡糖苷酶增加葡萄糖的产量,因此可广泛用于生物乙醇的经济生产。

    METHOD FOR REPROGRAMMING OF HUMAN DENTAL PULP CELL USING OCT4 AND SOX2 AND USE THEREOF
    46.
    发明申请
    METHOD FOR REPROGRAMMING OF HUMAN DENTAL PULP CELL USING OCT4 AND SOX2 AND USE THEREOF 审中-公开
    使用OCT4和SOX2重组人牙髓细胞的方法及其用途

    公开(公告)号:US20150299665A1

    公开(公告)日:2015-10-22

    申请号:US14340991

    申请日:2014-07-25

    Abstract: The present invention relates to a method for producing endothelial progenitor cells, comprising a method for producing induced pluripotent stem cells by using only Oct4 and Sox2 as a reprogramming factor of human dental pulp cells, and differentiating endothelial progenitor cells from the induced pluripotent stem cells produced by the method for producing induced pluripotent stem cells. Moreover, the present invention relates to a method for producing endothelial cells, comprising differentiating endothelial cells from endothelial progenitor cells produced by the method for producing the endothelial progenitor cells. Additionally, the present invention relates to a method for producing smooth muscle cells, comprising differentiating smooth muscle cells from endothelial progenitor cells produced by the method for producing the endothelial progenitor cells.Also, the present invention make a significant contribution to treatment of ischemia disease and heart disease because a patient's dental pulp cell-derived differentiated cells can be used for cell treatment as a result of the cell treatment effect of the endothelial progenitor cells in a mouse model induced to have hind limb ischemia or myocardial infarction.

    Abstract translation: 本发明涉及一种生产内皮祖细胞的方法,其包括通过仅使用Oct4和Sox2作为人牙髓细胞的重新编程因子来产生诱导的多能干细胞的方法,以及从产生的诱导多能干细胞分化内皮祖细胞 通过产生诱导多能干细胞的方法。 此外,本发明涉及一种生产内皮细胞的方法,其包括将内皮细胞与由内皮祖细胞产生的方法产生的内皮祖细胞分化。 此外,本发明涉及一种平滑肌细胞的制备方法,其包括通过用于产生内皮祖细胞的方法产生的内皮祖细胞分化平滑肌细胞。 此外,本发明对于缺血性疾病和心脏病的治疗有显着的贡献,因为患者的牙髓细胞衍生的分化细胞可以作为小鼠模型中内皮祖细胞的细胞处理效果的细胞治疗而使用 诱发后肢缺血或心肌梗死。

    Method of producing 3-hydroxypropionic acid from glycerol
    47.
    发明授权
    Method of producing 3-hydroxypropionic acid from glycerol 有权
    从甘油生产3-羟基丙酸的方法

    公开(公告)号:US09090919B2

    公开(公告)日:2015-07-28

    申请号:US13505111

    申请日:2009-10-29

    Abstract: The present invention relates to a novel method of producing 3-hydroxypropionic acid from glycerol, and more particularly to a method of producing 3-hydroxypropionic acid by culturing in a glycerol-containing medium a mutant microorganism obtained by amplifying an aldehyde dehydrogenase-encoding gene in a microorganism having the abilities to produce coenzyme B12 and produce 3-hydroxypropionic acid using glycerol as a carbon source. The present invention enables the fermentation of glycerol even under microaerobic or aerobic conditions without having to add coenzyme B12. Thus, the invention will be very suitable for the development of biological processes for producing large amounts of 3-hydroxypropionic acid.

    Abstract translation: 本发明涉及一种由甘油生产3-羟基丙酸的新方法,更具体地说,涉及一种通过在含甘油培养基中培养产生3-羟基丙酸的方法,该突变体微生物是通过扩增醛脱氢酶编码基因 具有生产辅酶B12并使用甘油作为碳源产生3-羟基丙酸的微生物。 本发明即使在微需氧或需氧条件下也可以发酵甘油,而不必加入辅酶B12。 因此,本发明将非常适用于生产大量3-羟基丙酸的生物方法的开发。

    G protein coupled receptor protein and use thereof
    49.
    发明授权
    G protein coupled receptor protein and use thereof 有权
    G蛋白偶联受体蛋白及其用途

    公开(公告)号:US09034327B2

    公开(公告)日:2015-05-19

    申请号:US13322304

    申请日:2009-09-07

    CPC classification number: C07K14/705 G01N33/5041

    Abstract: Disclosed are novel GPCR (G Protein Coupled Receptor) proteins and genes encoding the same. Also provided is the use of the proteins and the genes. Particularly, contemplated are a novel GPCR (G Protein Coupled Receptor) polypeptide, a polynucleotide coding for the same, a recombinant vector carrying the polynucleotide or a fragment thereof, host cells transformed with the vector, a transgenic animal infected with the vector. Also, a composition for detecting a cancer marker, comprising an agent capable of measuring the expression level of mRNA or protein of the GPCR polynucleotide, a kit for the diagnosis of cancer, comprising the composition, and a method for detecting the GPCR polypeptide and a gene encoding the polypeptide are provided. Further, a composition for the treatment and prevention of cancer, comprising an oligonucleotide inhibiting the expression of a gene encoding the GPCR polypeptide or an antibody against the GPCR protein, and a method for screening a modulator of the GPCR protein or a cancer therapeutic agent are provided.

    Abstract translation: 公开了新型GPCR(G蛋白偶联受体)蛋白和编码其的基因。 还提供了蛋白质和基因的使用。 特别地,考虑了新型GPCR(G蛋白偶联受体)多肽,编码它的多核苷酸,携带多核苷酸或其片段的重组载体,用该载体转化的宿主细胞,用载体感染的转基因动物。 另外,含有能够测定GPCR多核苷酸的mRNA或蛋白质的表达量的试剂,癌症诊断用试剂盒,含有该组合物的检测癌标记物的组合物,以及检测GPCR多肽的方法和 提供编码多肽的基因。 此外,用于治疗和预防癌症的组合物包含抑制GPCR多肽或编码GPCR蛋白的抗体表达的寡核苷酸以及筛选GPCR蛋白或癌症治疗剂的调节剂的方法, 提供。

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