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    • 12. 发明申请
    • COCHLEAR IMPLANT ASSEMBLY
    • COCHLEAR植物大会
    • WO2007065216A3
    • 2007-07-26
    • PCT/AU2006001855
    • 2006-12-06
    • COCHLEAR LTDKAISER THOMAS
    • KAISER THOMAS
    • A61N1/05H01B5/14
    • A61N1/0541
    • A method of forming electrode structures comprising a plurality of electrode pads (14) and a plurality of electrically conducting wires (16) with at least one wire (16) extending from at least one of the electrode pads (14). The method comprises coating an electrode structure with a relatively electrically insulating material, arranging each of the electrode pads (14) in a first arrangement; arranging the wires (16) relative to each other to provide a sufficient gap of separation between neighbouring wires (16); securing the wires (16) to a remotely positioned anchor member (30) to preserve a gap of separation between neighbouring wires (16), and applying a coating of relatively electrically insulating material to the electrode structure.
    • 一种形成电极结构的方法,包括多个电极焊盘(14)和多个导电线(16),其中至少一个导线(16)从至少一个电极焊盘(14)延伸。 该方法包括用相对电绝缘材料涂覆电极结构,以第一布置布置每个电极焊盘(14); 布置电线(16)以相对于彼此提供相邻电线(16)之间的足够的间隔间隔; 将电线(16)固定到远程定位的锚固构件(30)上以保持相邻导线(16)之间的间隔,并将相对电绝缘材料的涂层施加到电极结构。
    • 16. 发明专利
    • ASSAYS
    • AU2014200826B2
    • 2016-01-14
    • AU2014200826
    • 2014-02-17
    • CLONDIAG GMBH
    • ERMANTRAUT EUGENSCHULZ TORSTENKAISER THOMASSTEINMETZER KATRIN
    • C12Q1/68B01J19/00B01L3/00
    • Abstract A method, comprising (a) providing an amount of a reporter compound; a first binding member being configured to bind an anchor group of a capture molecule; a 5 second binding member capable of capturing the reporter compound; an amount of a target nucleic acid capable of forming complexes with the reporter compound, the forming of complexes with the reporter compound inhibiting capturing of the reporter compound by the second binding member; and an amount of capture molecules wherein each capture molecule comprises a binding portion specific to a 10 region of the target nucleic acid and an anchor group; (b) forming complexes each comprising a target nucleic acid and a capture molecule; (c) contacting the complexes with the first binding member to bind at least a subset of the complexes to the first binding member; (d) releasing at least a subset of the amount of target nucleic acid from the first binding member; (e) forming complexes of a subset of the 15 amount of reporter compound with at least a subset of the amount of target nucleic acid; (f) capturing a remaining subset of the amount of reporter compound not in complex with a target nucleic acid on the second binding member; and (g) determining a value indicative of the presence and/or amount of reporter compound captured on the second binding member.
    • 19. 发明专利
    • Microfluidic networks for performing assays
    • NZ580395A
    • 2012-02-24
    • NZ58039508
    • 2008-05-05
    • CLONDIAG GMBH
    • KAISER THOMASMOBIUS KLAUS-PETERSCHULZ TORSTENUHLIG THOMASVON SCHENK ZU SCHWEINSBERG ALEXANDERERMANTRAUT EUGENTUCHSCHEERER JENS
    • B01L3/00
    • Disclosed is a device for detecting an analyte, comprising: a) a cartridge having: a microfluidic channel including an inlet and a detection region in fluid communication with the inlet; b) a microfluidic flow path having an at least partially deformable wall and in fluid communication with the detection region of the channel; and c) a cap having: a sealing member configured to seal with the inlet and form a fluid circuit including the inlet, the microfluidic channel and the microfluidic flow path. Also disclosed is a method comprising: a) introducing a liquid sample into an inlet of a microfluidic channel thereby forming a contiguous liquid slug enclosed by the channel and bounded at a first end by a transport fluid, the liquid sample comprising multiple particles, b) sealing a sealing member of a cap with the inlet and thereby forming a fluid circuit such that the transport fluid provides fluid communication between the first and second ends of the liquid slug, c) forming a mixture comprising at least a portion of the liquid sample and an optical label present within the microfluidic channel by applying a differential pressure to the first and second ends of the liquid slug via the transport fluid and thereby moving the liquid slug within the fluid circuit, d) forming multiple complexes, each complex comprising one of the multiple particles and at least one of the optical labels, and e) detecting complexes present within a subset of the mixture.