公开(公告)号：EP1056882A4

公开(公告)日：2002-04-17

申请号：EP99909528

申请日：1999-02-19

申请人： WISYS TECHNOLOGY FOUNDATION

发明人： WISYS TECHNOLOGY FOUNDATION

IPC分类号： G01N33/53 ,  B01J19/00 ,  C07B61/00 ,  C07K1/04 ,  C07K17/00 ,  C12M1/00 ,  C12N15/09 ,  C12Q1/68 ,  C40B40/10 ,  G01N33/543 ,  G01N33/544 ,  G01N33/566 ,  G01N37/00

CPC分类号： G01N33/54366 ,  B01J19/0046 ,  B01J2219/00 ,  B01J2219/00515 ,  B01J2219/00518 ,  B01J2219/00538 ,  B01J2219/00585 ,  B01J2219/0059 ,  B01J2219/00596 ,  B01J2219/00657 ,  B01J2219/00659 ,  B01J2219/00707 ,  B01J2219/00725 ,  C07B2200/11 ,  C07K1/047 ,  C40B40/10

摘要： A method for the solid-phase synthesis of combinatorial libraries on a one-dimensional support, such as a thread, is provided. The method involves the cyclic permutation of structural features along the thread, in such a way that different structural features are repeated at a characteristic fixed frequencies along the thread. The thread is processed so as to generate a signal proportional to the activity of the compounds in the library, and the thread is then assayed by being drawn through an appropriate detector. The resulting time-domain signal is processed by Fourier transformation. Spikes in the frequency domain of the processed signal indicate the frequency at which structural features that contribute to the activity were created on the thread.

公开(公告)号：EP2909343B1

公开(公告)日：2018-10-10

申请号：EP13846570.3

申请日：2013-10-16

申请人： Abbott Molecular Inc.

发明人： HAYDEN, Mark A.

IPC分类号： C12Q1/6869

CPC分类号： C12Q1/6874 ,  B01J2219/00 ,  B01J2219/005 ,  C12Q1/6869 ,  C12Q2563/159

摘要： Methods, systems, apparatus and machine readable media are disclosed to sequence nucleic acid. An example method includes subjecting a sequence of target nucleotide bases captured on a microtransponder to a plurality of sequencing reactions to build a sequence of labeled nucleotide bases that are complementary to and bound to the sequence of target nucleotide bases. The example method also includes identifying each labeled nucleotide base of the sequence of labeled nucleotide bases and each respective complementary target nucleotide base of the sequence of target nucleotide bases to which the labeled nucleotide base is bound after each sequencing reaction. In addition, each labeled nucleotide base of the sequence of labeled nucleotide bases and each respective complementary target nucleotide base of the sequence of target nucleotide bases to which the labeled nucleotide base is bound is associated with a microtransponder identification number.

公开(公告)号：EP3106220A1

公开(公告)日：2016-12-21

申请号：EP16174701.9

申请日：2016-06-16

申请人： Southern Research Institute

发明人： GOYAL, Amit ,  GANGWAL, Santosh ,  LUCERO, Andrew

IPC分类号： B01J23/755 ,  B01J23/88 ,  B01J37/08 ,  B01J35/00 ,  B01J35/10 ,  C01B3/04 ,  C01B3/40 ,  B01J8/00 ,  C10J3/00 ,  H01M4/90

CPC分类号： B01J23/883 ,  B01J7/02 ,  B01J8/0005 ,  B01J19/245 ,  B01J23/002 ,  B01J23/005 ,  B01J23/755 ,  B01J23/88 ,  B01J35/0006 ,  B01J35/002 ,  B01J35/006 ,  B01J35/1014 ,  B01J35/1038 ,  B01J35/1061 ,  B01J37/0018 ,  B01J37/04 ,  B01J37/088 ,  B01J2219/00 ,  B01J2219/00033 ,  B01J2219/24 ,  B01J2523/00 ,  C01B3/382 ,  C01B3/40 ,  C01B2203/0233 ,  C01B2203/0244 ,  C01B2203/025 ,  C01B2203/0485 ,  C01B2203/062 ,  C01B2203/066 ,  C01B2203/1058 ,  C01B2203/1088 ,  C01B2203/1241 ,  C01B2203/141 ,  C10G2/30 ,  C10G5/00 ,  C10J3/00 ,  C10J3/72 ,  C10J2300/0913 ,  C10J2300/0916 ,  C10J2300/093 ,  C10J2300/0956 ,  C10J2300/0959 ,  C10J2300/0976 ,  C10J2300/1618 ,  C10J2300/1659 ,  C10K1/004 ,  C10K1/005 ,  C10K3/04 ,  H01M4/9025 ,  Y02E20/18 ,  Y02E60/364 ,  Y02P20/52 ,  B01J2523/31 ,  B01J2523/847 ,  B01J2523/68

摘要： Nickel based catalyst structures are described herein that include a plurality of metal oxides formed as crystalline phases within the catalyst structures. Each metal oxide of a catalyst structure includes nickel and/or aluminum, where one or more metal oxides includes a nickel aluminum oxide, and the one or more nickel aluminum oxides is greater than 50% by weight of the crystalline phases within the catalyst structure. The catalyst structures further have specific surface areas of at least 13 m 2 /g. Mixed nickel aluminates such as the spinel phase, NiAl 2 O 4 , and NiAl 10 O 16 are shown to have a high stability in reforming reactions.
The catalyst structures are resistant to high concentrations of sulfur and are effective in reforming operations for converting methane and other light hydrocarbons to hydrogen and one or more other components. For example, the catalyst structures are effective in coal and biomass gasification systems for the forming and cleanup of synthetic gas.

摘要翻译： 没有被描述在镍基催化剂结构包括形成为催化剂结构内的结晶相的金属氧化物的复数。 催化剂结构中的每一个金属氧化物包括镍和/或铝，其中一个或多个金属氧化物包括氧化镍铝，和所述一个或多个镍铝的氧化物大于50重量％的催化剂结构内的晶相的。 催化剂结构还具有至少13米2 /克的比表面积。 混合的镍铝酸盐：如尖晶石相，的NiAl 2 O 4和NiAl金属10 O 16被示出为具有在重整反应的高稳定性。 所述的催化剂结构，以硫的高浓度的抗性和能有效地用于将甲烷和其它轻质烃类和氢的一种或多种其它组分的重整操作。 例如，催化剂结构用于成形和合成气体的净化有效煤和生物质气化系统。

公开(公告)号：EP2984597A4

公开(公告)日：2016-10-19

申请号：EP14783290

申请日：2014-04-11

申请人： ELLUME PTY LTD

发明人： PARSONS SEAN ANDREW ,  DAHL STEVEN DAVID ,  EDGECOMBE JONATHAN PETER

IPC分类号： G06F19/00 ,  G01N33/50

CPC分类号： G01N33/558 ,  B01J2219/00 ,  G01N33/48771 ,  G16H10/40

摘要： A test device comprises first and second indicia portions. The first indicia portion is configured to indicate the presence or absence of at least one medical condition based on identification of at least one biological entity in the biological sample. The second indicia portion is configured to display all or part of a composite code when the first indicia portion provides an indication of the presence of the medical condition, the code being substantially unique to the test device. The test device includes a printed circuit board and a portion of the composite code corresponds to a serial number of the printed circuit board.

公开(公告)号：EP2984597A1

公开(公告)日：2016-02-17

申请号：EP14783290.1

申请日：2014-04-11

申请人： Ellume Pty Ltd.

发明人： PARSONS, Sean Andrew ,  DAHL, Steven David ,  EDGECOMBE, Jonathan Peter

IPC分类号： G06F19/00 ,  G01N33/50

CPC分类号： G01N33/558 ,  B01J2219/00 ,  G01N33/48771 ,  G16H10/40

摘要： A test device comprises first and second indicia portions. The first indicia portion is configured to indicate the presence or absence of at least one medical condition based on identification of at least one biological entity in the biological sample. The second indicia portion is configured to display all or part of a composite code when the first indicia portion provides an indication of the presence of the medical condition, the code being substantially unique to the test device. The test device includes a printed circuit board and a portion of the composite code corresponds to a serial number of the printed circuit board.

公开(公告)号：EP1056882A1

公开(公告)日：2000-12-06

申请号：EP99909528.4

申请日：1999-02-19

申请人： Schwabacher, Alan W.

发明人： Schwabacher, Alan W.

IPC分类号： C12Q1/00 ,  C12Q1/68 ,  G01N21/84 ,  G01N33/53 ,  G01N33/566 ,  G01N33/543 ,  G01N33/544

CPC分类号： G01N33/54366 ,  B01J19/0046 ,  B01J2219/00 ,  B01J2219/00515 ,  B01J2219/00518 ,  B01J2219/00538 ,  B01J2219/00585 ,  B01J2219/0059 ,  B01J2219/00596 ,  B01J2219/00657 ,  B01J2219/00659 ,  B01J2219/00707 ,  B01J2219/00725 ,  C07B2200/11 ,  C07K1/047 ,  C40B40/10

摘要： A method for the solid-phase synthesis of combinatorial libraries on a one-dimensional support, such as a thread, is provided. The method involves the cyclic permutation of structural features along the thread, in such a way that different structural features are repeated at a characteristic fixed frequencies along the thread. The thread is processed so as to generate a signal proportional to the activity of the compounds in the library, and the thread is then assayed by being drawn through an appropriate detector. The resulting time-domain signal is processed by Fourier transformation. Spikes in the frequency domain of the processed signal indicate the frequency at which structural features that contribute to the activity were created on the thread.