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    • 3. 发明申请
    • PHARMACEUTICAL COMPOSITION FOR TREATING GROWTH HORMONE DEFICIENCY CONTAINING hGH FUSION PROTEIN
    • 用于治疗含有hGH融合蛋白的生长激素缺乏的药物组合物
    • WO2018044060A1
    • 2018-03-08
    • PCT/KR2017/009471
    • 2017-08-30
    • GENEXINE,INC.HANDOK INC.
    • KIM, Tae KyungWOO, Jung WonLEE, Joan Yoon JiAHN, Young-JooCHA, Ji-EunRHIM, Hyou YoungJANG, Woo Ick
    • A61K38/16A61K38/27
    • The present disclosure relates to a method for administering a human growth hormone fusion protein (GX-H9) for treating growth hormone deficiency. Specifically, the present disclosure relates to a pharmaceutical composition for treating growth hormone deficiency, which comprises an hGH fusion protein (GX-H9) and a pharmaceutically acceptable carrier, wherein the fusion protein (GX-H9) is administered once a week at a dose of 0.4 to 1.6 mg per body weight kg of a pediatric patient, or administered once every two weeks at a dose of 0.8 to 3.2 mg per body weight kg of a pediatric patient. In addition, the present disclosure relates to a method for treating growth hormone deficiency, which comprising a step of administering an hGH fusion protein (GX-H9) to a patient with growth hormone deficiency once a week at a dose of 0.4 to 1.6 mg per body weight kg of the patient, or once every two weeks at a dose of 0.8 to 3.2 mg per body weight kg of the patient.
    • 本公开涉及用于施用人生长激素融合蛋白(GX-H9)以治疗生长激素缺乏症的方法。 具体而言,本公开涉及用于治疗生长激素缺乏的药物组合物,其包含hGH融合蛋白(GX-H9)和药学上可接受的载体,其中所述融合蛋白(GX-H9)每周一次以剂量 体重每公斤体重0.4至1.6mg的儿科患者,或者每两周以0.8至3.2mg剂量每公斤体重的儿科患者施用一次。 另外,本公开涉及用于治疗生长激素缺乏症的方法,其包括将hGH融合蛋白(GX-H9)以每周0.4-1.6mg的剂量给予患有生长激素缺乏的患者一周一次的步骤 体重kg的患者,或者每两周一次,剂量为0.8-3.2mg / kg体重的患者。
    • 6. 发明申请
    • MEDIUM COMPOSITION FOR PREPARING BOTULINUM TOXIN
    • 用于制备BOTULINUM TOXIN的中间组合物
    • WO2016175567A1
    • 2016-11-03
    • PCT/KR2016/004432
    • 2016-04-28
    • DAEWOONG CO., LTD.
    • KIM, Kyoung-YunSUL, Hye-YoungMIN, Kyoung-Min
    • C12N5/00C07K14/33
    • C12N9/52C07K14/33C12N1/20C12Y304/24069
    • The present invention relates to a medium composition for production of botulinum toxin and, more particularly, to a medium composition for culture of Clostridium sp. capable of producing botulinum toxin. The medium composition of the present invention comprises a porcine peptone and at least one plant-derived peptone selected from the group consisting of a garden pea hydrolysate, a cotton seed hydrolysate and a wheat gluten hydrolysate. When the medium according to the present invention, which contains plant-derived peptones, porcine peptones and minerals, is used for culture of Clostridium botulinum , the growth rate of the bacterium in the medium is higher than that in each of the medium that is in current use and the medium comprising plant-derived peptones alone. In addition, when the medium of the present invention is used, a high concentration of botulinum toxin can be produced by culturing the bacterium in a safe manner.
    • 本发明涉及用于生产肉毒杆菌毒素的培养基组合物,更具体地说,涉及用于培养梭菌属的培养基组合物。 能够产生肉毒杆菌毒素。 本发明的培养基组合物包含猪蛋白胨和至少一种选自花生豌豆水解产物,棉花种子水解物和小麦麸质水解产物的植物来源的蛋白胨。 当将含有植物来源的胨,猪胨和矿物质的本发明的培养基用于肉毒杆菌的培养时,培养基中细菌的生长速度高于培养基中培养的培养基 目前的用途和包含单独植物来源的胨的培养基。 此外,当使用本发明的培养基时,可以通过以安全的方式培养细菌来产生高浓度的肉毒杆菌毒素。
    • 8. 发明申请
    • Melting curve analysis using PNA probe, Method and Kit for analyzing Nucleotide Polymorphism using melting curve analysis
    • 使用PNA探针的熔解曲线分析,使用熔解曲线分析分析核苷酸多态性的方法和试剂盒
    • WO2015152446A1
    • 2015-10-08
    • PCT/KR2014/002909
    • 2014-04-04
    • PANAGENE INC.
    • JOE, Goon HoKIM, Sung-KeePARK, HeekyungPARK, Chwang SiekKIM, Se RyunKIM, YongtaeKIM, Su Nam
    • C12Q1/68
    • C12Q1/6818C12Q2525/107C12Q2527/107C12Q2563/173
    • Provided are a PNA probe for detecting nucleotide polymorphism of a target gene, a melting curve analysis method for detecting the nucleotide polymorphism of the target gene using the same, a nucleotide polymorphism analysis method of a target gene including the melting curve analysis method, and a kit for detecting the nucleotide polymorphism of the target gene containing the PNA probe. It is characterized that the PNA probe according to the present invention contains negative charge molecules. The modified PNA probe according to the present invention contains the negative charge molecules to have a high recognition ability with respect to a target DNA and a high coupling ability to the target DNA and to be rapidly dissociated by heat, such that the nucleotide polymorphism analysis may be relatively easily performed even in a heterozygous sample showing two melting curve graphs, and two or more adjacent single nucleotide polymorphisms may be simultaneously analyzed.
    • 提供了用于检测靶基因的核苷酸多态性的PNA探针,使用该靶基因的靶基因的核苷酸多态性的检测的解链曲线分析方法,包含解链曲线分析法的靶基因的核苷酸多态性分析方法,以及 用于检测含有PNA探针的靶基因的核苷酸多态性的试剂盒。 其特征在于根据本发明的PNA探针含有负电荷分子。 根据本发明的修饰的PNA探针含有相对于目标DNA具有高识别能力的负电荷分子和与目标DNA的高偶联能力并且通过热快速解离,使得核苷酸多态性分析可以 即使在显示两个解链曲线图的杂合样品中也可以相对容易地进行,并且可以同时分析两个或更多个相邻的单核苷酸多态性。