会员体验
专利管家(专利管理)
工作空间(专利管理)
风险监控(情报监控)
数据分析(专利分析)
侵权分析(诉讼无效)
联系我们
交流群
官方交流:
QQ群: 891211   
微信请扫码    >>>
现在联系顾问~
热词
    • 6. 发明授权
    • Method of calibrating ligand specificity
    • 校准配体特异性的方法
    • US07923211B2
    • 2011-04-12
    • US12543801
    • 2009-08-19
    • Akito TanakaAkira Yamazaki
    • Akito TanakaAkira Yamazaki
    • G01N33/53G01N33/543
    • G01N33/54313G01N33/54393Y10S435/973Y10T436/10Y10T436/25375
    • A method to determine specificity of ligand binding includes comparing a solid phase carrier first extract obtained by pre-treating a sample with a ligand-immobilized solid phase carrier and a solid phase carrier second extract obtained by treating the pretreated sample again with a ligand-immobilized solid phase carrier in terms of the proteins contained therein, and identifying a protein whose content is remarkably decreased in the second extract compared to the first extract, in order to solve 1) the problem of the solubility of subject ligand, 2) the problem of the non-specific protein-denaturing effect of the subject ligand added, and the like, in antagonism experiments in target search using an affinity resin.
    • 确定配体结合特异性的方法包括比较通过预处理样品与固定配体的固相载体获得的固相载体第一提取物和通过用配体固定化处理再次处理预处理的样品获得的固相载体第二提取物 固相载体与其中所含的蛋白质相比,并鉴定出与第一提取物相比,第二提取物中其含量显着降低的蛋白质,以解决1)本发明配体的溶解度问题,2) 使用亲和树脂进行目标检测的拮抗实验中加入的受试者配体的非特异性蛋白质变性效应等。
    • 7. 发明申请
    • METHOD FOR EFFECTIVE SEARCH FOR TARGET MOLECULE
    • 有效搜索目标分子的方法
    • US20090042318A1
    • 2009-02-12
    • US11814986
    • 2006-01-26
    • Akito TanakaAkira YamazakiMasayuki Haramura
    • Akito TanakaAkira YamazakiMasayuki Haramura
    • G01N33/545
    • G01N33/54393B01J20/3227B01J20/3248B01J20/3253B01J20/3255B01J20/3285G01N33/54306
    • The present invention provides a solid phase carrier capable of adsorbing a highly hydrophobic target molecule, for example, a membrane associated protein, and a solid phase carrier optimized not only for a highly hydrophobic target molecule, but also for an optionally chosen target molecule. More specifically, the present invention provides a solid phase carrier having a ligand and a capping agent immobilized thereon, with the hydrophobic property of the surface thereof adjusted to enable the binding of the target molecule to the ligand, or to increase the amount of target molecule bound to the ligand; various methods using the solid phase carrier (for example, method of concentrating, isolating, or purifying a target molecule, a method of selectively adsorbing a particular target molecule to the solid phase carrier, or a method of analyzing the interaction between ligand and target molecule therefor); a production method for the solid phase carrier; and an improvement method for a solid phase carrier having a ligand and a capping agent immobilized thereon and the like.
    • 本发明提供了能够吸附高度疏水的靶分子例如膜相关蛋白的固相载体,以及不仅对于高度疏水的靶分子而且优选任选地选择的靶分子优化的固相载体。 更具体地说,本发明提供一种具有固定在其上的配体和封端剂的固相载体,其表面的疏水性被调节以使靶分子与配体结合,或增加靶分子的量 与配体结合; 使用固相载体的各种方法(例如,浓缩,分离或纯化靶分子的方法,将特定靶分子选择性吸附到固相载体上的方法或分析配体与靶分子之间的相互作用的方法 为此) 一种固相载体的制备方法; 以及其上固定有配体和封端剂等的固相载体的改进方法。
    • 10. 发明申请
    • Method of calibrating ligand specificity
    • 校准配体特异性的方法
    • US20070122913A1
    • 2007-05-31
    • US10573167
    • 2004-10-15
    • Akito TanakaAkira Yamazaki
    • Akito TanakaAkira Yamazaki
    • G01N33/558
    • G01N33/54313G01N33/54393Y10S435/973Y10T436/10Y10T436/25375
    • In a method comprising comparing a solid phase carrier extract 1 obtained by pre-treating a sample with a ligand-immobilized solid phase carrier and a solid phase carrier extract 2 obtained by treating the pretreated sample again with a ligand-immobilized solid phase carrier in terms of the proteins contained therein, and identifying a protein whose content is remarkably decreased in the extract 2 compared to the extract 1, 1) the problem of the solubility of subject ligand, 2) the problem of the non-specific protein-denaturing effect of the subject ligand added, and the like, which have been problematic in antagonism experiments in target search using an affinity resin, have been solved.
    • 在包括将通过预处理样品获得的固相载体提取物1与固定配体的固相载体和固相载体提取物2进行比较的方法中,所述固相载体提取物2通过用配体固定的固相载体再次处理预处理的样品而得到 的蛋白质,并且鉴定与提取物1相比,提取物2中的含量显着降低的蛋白质,1)主体配体的溶解度的问题,2)非特异性蛋白质变性效应的问题 已经解决了使用亲和性树脂在靶搜索中的拮抗实验中存在问题的添加的受试者配体等。