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
    • 2. 发明申请
    • PREPARING AND ANALYZING SOLID FORM PROPERTIES OF A SUBSTANCE
    • 一种物质的固体形态的制备和分析
    • WO2018078129A1
    • 2018-05-03
    • PCT/EP2017/077665
    • 2017-10-27
    • F. HOFFMANN-LA ROCHE AGHOFFMANN-LA ROCHE INC.
    • SCHWITTER, UrsRAN, FrédéricALKER, AndréKISSLING, TomZUMSTEIN, Thomas
    • B01L3/00B01L3/06
    • In a method of analyzing solid form properties of a substance, which comprising the step of solidifying the substance, the solidified substance is obtained in one of a plurality of wells (1, 46) of a multi-well plate (4). In the multi-well plate (4) the at least one of the plurality of wells (1, 46) has a bottom (22) made of a thermoplastic polyimide. The method further comprises analyzing the solidified substance in the well (1, 46) of the multi-well plate (4) by X-ray diffraction. Thereby, said analysis comprises providing X-ray through the solidified substance and a bottom (22) of the well (1, 46) and evaluating the X-ray which passed the solidified substance and the bottom (22) of the well (1, 46). Such method and multi-well plate (4) provide a durable and cost efficient system allowing a high quality analysis of solid form properties of the substance and an efficient and safe processing of the substance.
    • 在分析包括固化物质的步骤的物质的固体形态性质的方法中,固化的物质在多级多孔体(1,46)中的一个中获得, (4)。 在多孔板(4)中,多个井(1,46)中的至少一个具有由热塑性聚酰亚胺制成的底部(22)。 该方法还包括通过X射线衍射分析多孔板(4)的孔(1,46)中的固化物质。 因此,所述分析包括提供穿过固化物质和井(1,46)的底部(22)的X射线并且评估穿过固化物质和井(1,46)的底部(22)的X射线, 46)。 这种方法和多孔板(4)提供了耐用且成本有效的系统,允许高质量地分析该物质的固体形式特性以及该物质的有效且安全的处理。
    • 3. 发明申请
    • METHOD OF LOADING A CRYSTALLIZATION DEVICE
    • 装载结晶装置的方法
    • WO2010037510A1
    • 2010-04-08
    • PCT/EP2009/006964
    • 2009-09-28
    • QIAGEN GMBHKUBICEK, JohannSCHÄFER, FrankLABAHN, JörgBÜLDT, GeorgFORSCHUNGSZENTRUM JÜLICH GMBH(FJZ)
    • KUBICEK, JohannSCHÄFER, FrankLABAHN, JörgBÜLDT, Georg
    • B01D9/00C30B7/00C30B29/58B01L3/06
    • C07K1/306B01D9/00B01D9/0077B01D2009/0086B01L3/06C07K14/705
    • The present invention pertains to a method for loading a crystallization device and for manufacturing a crystallization device comprising multiple receptacles with a pre-defined amount of at least one matrix-forming compound capable of forming a crystallization matrix for a membrane protein, said method comprising the following steps: a) Modifying the state of aggregation of said at least one matrix-forming compound to a fluidic state which allows dispensing said at least one matrix-forming compound, and b) dispensing a defined amount of said at least one matrix-forming compound into at least one receptacle of the crystallization device, wherein said dispensed matrix-forming compound solidifies within said receptacle. Thereby, prefilled crystallization devices are obtained which can be used as consumables in particular in automated crystallization processes. Also provided are protein crystallization methods using respectively prepared crystallization devices.
    • 本发明涉及一种用于装载结晶装置和用于制造结晶装置的方法,所述结晶装置包括具有预定量的至少一种能够形成膜蛋白质的结晶基质的基质形成化合物的多个容器,所述方法包括 以下步骤:a)将所述至少一种基质形成化合物的聚集状态改变为允许分配所述至少一种基质形成化合物的流体状态,以及b)分配限定量的所述至少一种基质形成 化合物进入结晶装置的至少一个容器中,其中所述分配的基质形成化合物在所述容器内固化。 因此,获得了可以用作消费品,特别是在自动结晶过程中的预填充结晶装置。 还提供了使用分别制备的结晶装置的蛋白质结晶方法。
    • 4. 发明申请
    • MICROFLUIDIC DEVICES AND METHODS FOR PROTEINS CRYSTALLIZATION AND IN SITU X-RAY DIFFRACTION
    • 蛋白质结晶和X射线衍射的微流体装置和方法
    • WO2009150549A3
    • 2010-04-01
    • PCT/IB2009006586
    • 2009-06-15
    • SPINX INCZUCCHELLI PIERO
    • ZUCCHELLI PIERO
    • B01L3/06B01D9/00B01L3/00C30B7/00C30B29/58
    • B01L3/06B01D9/00B01D9/0072B01D9/0077B01L3/5025B01L3/5027B01L2200/0621B01L2200/10B01L2200/12B01L2300/0816B01L2300/0819B01L2300/0854B01L2300/087B01L2300/0887B01L2400/0409B01L2400/0683C30B7/00C30B29/58
    • The present disclosure is directed generally to devices and methods with the purpose of interfacing micro fluidic devices with dispensing and fluid handling systems to achieve the rapid identification of protein crystallization conditions. The device described herein is fabricated with the use of a cyclic olefin homopolymer-based creating microfluidics system adaptable for protein crystallization and in situ X-ray diffraction. Connectivity between chambers is controlled by valves that allow specified volumes of liquid to be transferred from one chamber to another. The microfluidic system is useful to established microbatch, vapor diffusion and free interface diffusion protocols for protein crystallization and to obtain crystals for a number of proteins, including chicken lysozyme, bovine trypsin, a human p53 protein containing both the DNA binding and oligomerization domains bound to DNA and a functionally important domain of Arabidopsis Morpheus' Molecule 1 (MOMl). For X-ray diffraction analysis, either the microfluidic devices were opened to allow mounting of the crystals on loops or the crystals were exposed to X-rays in situ. Thus, cyclic olefin homopolymer-based microfluidics systems are useful to further automate protein crystallization and structural genomics efforts.
    • 本公开通常涉及用于将微流体装置与分配和流体处理系统接合以实现蛋白质结晶条件的快速鉴定的装置和方法。 本文描述的装置使用适用于蛋白质结晶和原位X射线衍射的基于环烯烃均聚物的产生微流体系统来制造。 室之间的连通性由阀控制,允许指定体积的液体从一个室转移到另一个室。 微流体系统可用于建立蛋白质结晶的微批,蒸汽扩散和自由界面扩散方案,并获得许多蛋白质的晶体,包括鸡溶菌酶,牛胰蛋白酶,含有结合到DNA结合和寡聚结构域的人p53蛋白 DNA和功能重要的拟南芥Morpheus分子1(MOM1)的结构域。 对于X射线衍射分析,打开微流体装置以允许将晶体安装在环上或将晶体原位暴露于X射线。 因此,环烯烃均聚物基微流体系统可用于进一步自动化蛋白质结晶和结构基因组学研究。
    • 6. 发明申请
    • METHODS AND DEVICES FOR HIGH THROUGHPUT CRYSTALLIZATION
    • 用于高通量结晶的方法和装置
    • WO02042731A2
    • 2002-05-30
    • PCT/US2001/042968
    • 2001-11-20
    • B01J19/00B01L3/00B01L3/06C30B7/00C40B60/14G01N
    • B01J19/0046B01J2219/00274B01J2219/00313B01J2219/0043B01J2219/00443B01J2219/00585B01J2219/00659B01J2219/00707B01J2219/00756B01L3/06B01L3/5085B01L2300/0896B01L2300/16B82Y15/00B82Y30/00C30B7/00C30B29/58C40B60/14
    • Crystallization apparatus (20) and methods which allow for fast screening and determination of protein crystallization conditions with small protein quantities and rapid crystallization. The apparatus comprise a first region comprising a first nucleation catalyst material (36) and a second region comprising a second nucleation catalyst material (38), with the first and second regions positioned adjacent to each other and configured to support at least one crystal, and with the first region having a variation in a nucleation property of the first nucleation catalyst material (36), in the first region. The crystal may be supported at an interface of the adjacent regions. The methods comprise providing a first region of a first nucleation catalyst material (36) and a second region of a second nucleation catalyst material (38) adjacent said first region, with the first region having a variation in a nucleation property of the first nucleation catalyst material (36), exposing the first and second regions to a solution of a selected molecule, and growing at least one crystal of the molecule in association with the first and second regions.
    • 结晶装置(20)和允许快速筛选和测定具有小蛋白质量和快速结晶的蛋白质结晶条件的方法。 该装置包括第一区域,其包括第一成核催化剂材料(36)和包含第二成核催化剂材料(38)的第二区域,其中第一和第二区域彼此相邻并且被配置为支持至少一个晶体,以及 其中第一区域在第一区域具有第一成核催化剂材料(36)的成核性质的变化。 晶体可以在相邻区域的界面处被支撑。 所述方法包括提供第一成核催化剂材料(36)的第一区域和邻近所述第一区域的第二成核催化剂材料(38)的第二区域,其中第一区域具有第一成核催化剂的成核性能的变化 材料(36),将所述第一和第二区域暴露于所选择的分子的溶液,并且与所述第一和第二区域相关联地生长所述分子的至少一个晶体。