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    • 42. 发明申请
    • METHODS AND APPARATUS FOR MEASURING THE LIGHT ABSORBANCE OF A SUBSTANCE IN A SOLUTION
    • 用于测量溶液中物质的光吸收的方法和装置
    • US20150153272A1
    • 2015-06-04
    • US14404860
    • 2013-05-30
    • GE HEALTHCARE BIO-SCIENCES AB
    • Hanno EhringFredrik Lars JarhedeErik Ostlund
    • G01N21/33
    • G01N21/33G01N21/3151G01N30/74G01N2021/3181G01N2030/8827G01N2201/062
    • Disclosed is an apparatus for measuring the absorbance of a substance in a solution, comprising: i) a sample cell (30) of known path length (b) for containing said solution (S), said cell being transparent to light of a predefined wavelength spectrum; ii) plural LED's each being independently operable by means of a controller (25) each for emitting light, within said predefined wavelength spectrum, along a light path; iii) a band pass filter (22) in the light path; iv) a beam splitter (24) for dividing light from said source propagating along the path into a first portion and a second portion, said first portion being directable by the beam splitter toward a reference detector (42) and said second portion being directable into the cell (30); v) a reference detector (42) for detecting the intensity of said first portion of light directed by said beam splitter; and vi) a sample detector (40) for detecting the intensity of the second portion propagating from the cell; the apparatus allowing a sample in the cell to be inexpensively subjected to more than one wavelength of light for quicker or more accurate analysis.
    • 公开了一种用于测量溶液中物质的吸光度的装置,包括:i)用于容纳所述溶液(S)的已知路径长度(b)的样品池(30),所述池对于预定波长的光是透明的 光谱; ii)多个LED各自可以通过控制器(25)独立操作,每个控制器用于沿所述光路在所述预定波长光谱内发射光; iii)光路中的带通滤波器(22); iv)用于将沿着路径传播的光源的光分离成第一部分和第二部分的分束器(24),所述第一部分可被分束器引向参考检测器(42),并且所述第二部分可被引导到 细胞(30); v)用于检测由所述分束器引导的所述第一部分光的强度的参考检测器(42) 和vi)用于检测从单元传播的第二部分的强度的样本检测器(40) 允许细胞中的样品经济地经受多于一个波长的光的装置,用于更快或更准确的分析。
    • 45. 发明授权
    • Method for determination of macromolecular multimers
    • 高分子多聚体测定方法
    • US08921120B2
    • 2014-12-30
    • US13503391
    • 2010-10-22
    • Ewa Pol
    • Ewa Pol
    • G01N33/566C07K1/14G01N33/543
    • C07K1/14G01N33/54373
    • A method of determining multimers of a macromolecule monomer in a sample containing the macromolecule comprises the steps of (i) determining the total concentration of macromolecule in the sample, (ii) determining by a biosensor-based detection method, especially mass-sensing, the active concentration of macromolecule in the sample, wherein physical characteristics of the macromolecule monomer are used, (iii) comparing the relationship of determined active macromolecule concentration to total macromolecule concentration for the sample with a corresponding relationship for an at least substantially multimer-free macromolecule-containing sample, and (iv) from a resulting difference determining the presence of multimers in the sample. The method may be used in the purification of macromolecules, such as proteins.
    • 在含有大分子的样品中测定高分子单体的多聚体的方法包括以下步骤:(i)测定样品中大分子的总浓度,(ii)通过基于生物传感器的检测方法,特别是质量感测, 样品中的高分子的活性浓度,其中使用大分子单体的物理特性,(iii)比较所测定的活性大分子浓度与样品的总大分子浓度的关系,其对应于至少基本上不含多聚体的大分子 - (iv)从得到的差异确定样品中多聚体的存在。 该方法可用于纯化大分子如蛋白质。
    • 47. 发明申请
    • PURIFICATION OF NUCLEIC ACID
    • 纯化核酸
    • US20140272999A1
    • 2014-09-18
    • US14352122
    • 2012-10-25
    • GE HEALTHCARE BIO-SCIENCES AB
    • Camilla Estmer NilssonJohan Ohman
    • C12N15/10C12Q1/68
    • C12Q1/6806C12N15/1006C12N15/1013C12N15/1017
    • The present invention relates to a simple and efficient method to isolate and purify nucleic acids, preferably genomic DNA, from complex samples compared with available methods, by using a ligand which relies on hydrogen bonding to purify the nucleic acids. Preferably the ligand is bound to magnetic beads/particles. More closely the method comprises adding a sample comprising nucleic acid to a polymer having neutral charge; reversibly binding said nucleic acid to said polymer by hydrogen bonding under pH conditions 5. The method is very suitable for sample preparation of nucleic acids, for example for PCR applications.
    • 本发明涉及通过使用依赖于氢键来提纯核酸的配体,与可用的方法相比,从复杂样品中分离和纯化核酸,优选基因组DNA的简单而有效的方法。 优选地,配体结合磁珠/颗粒。 更紧密地,该方法包括将含有核酸的样品添加到具有中性电荷的聚合物中; 在PH条件<5下通过氢键可逆地将所述核酸结合到所述聚合物上; 洗涤所述聚合物; 并在pH> 5的条件下从所述聚合物中洗脱所述核酸。 该方法非常适用于核酸的样品制备,例如用于PCR应用。
    • 48. 发明申请
    • PARALLEL ASSEMBLY OF CHROMATOGRAPY COLUMN MODULES
    • 色谱柱模块的平行组装
    • US20140263012A1
    • 2014-09-18
    • US14290357
    • 2014-05-29
    • GE HEALTHCARE BIO-SCIENCES AB
    • KLAUS GEBAUER
    • B01D15/14
    • B01D15/14B01D15/1864B01D15/1885B01D15/22G01N30/466G01N30/6039G01N30/6043G01N30/6091G01N2030/8881Y10T29/49826
    • A parallel assembly (2; 11; 51) of chromatography column modules (3a,b,c; 13a,b,c; 53a,b,c, 90a, b), the assembly having one common assembly inlet (15; 55) and one common assembly outlet (17; 57), each column module comprising a bed space (29) filled with chromatography medium and each column module comprises integrated fluid conduits which when the column module is connected with other column modules are adapted to connect the bed space (29) of the column module with the assembly inlet (15; 55) and the assembly outlet (17; 57), wherein the total length and/or volume of the fluid conduit from the assembly inlet to one bed space together with the length and/or volume of the fluid conduit from the same bed space to the assembly outlet is substantially the same for all bed spaces and modules installed in the parallel assembly.
    • 色谱柱模块(3a,b,c; 13a,b,c; 53a,b,c,90a,b)的平行组件(2; 11; 51),该组件具有一个共同的组装入口(15; 55) 和一个共同组装出口(17; 57),每个柱模块包括填充有色谱介质的床空间(29),并且每个柱模块包括集成流体导管,当列模块与其他柱模块连接时,适于连接床 柱模块的空间(29)与组件入口(15; 55)和组件出口(17; 57)相连,其中流体导管从组装入口到一个床空间的总长度和/或体积与 从同一床空间到组装出口的流体导管的长度和/或体积对于安装在平行组件中的所有床空间和模块基本相同。