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    • 1. 发明授权
    • Apparatus and method for sample delivery
    • 用于样品传送的装置和方法
    • US06605475B1
    • 2003-08-12
    • US09293314
    • 1999-04-16
    • Todd A. TaylorWilliam W. CarsonXian-Wei Yao
    • Todd A. TaylorWilliam W. CarsonXian-Wei Yao
    • G01N110
    • G01N27/44791G01N27/44743Y10T436/2575
    • Apparatus and methods have been developed to deliver automatically a sample to a reaction vessel, an analytical device or any location where sample introduction or deposition is desired. A sample delivery system of the invention generally includes a housing defining a channel, e.g., a capillary, and a volume controller, which is a temperature control device, in thermal communication with the channel. The channel preferably is closed at one end, and contains an opening for introduction of a sample. The closed end of the channel is associated thermally with the temperature control device. The temperature control device heats and cools a thermally expandable fluid in the channel which controls movement of a sample into, within and out of the channel.
    • 已经开发了装置和方法,以将样品自动递送到反应容器,分析装置或需要样品引入或沉积的任何位置。 本发明的样品输送系统通常包括限定通道的壳体,例如毛细管,以及与通道热连通的温度控制装置的体积控制器。 通道优选在一端封闭,并且包含用于引入样品的开口。 通道的封闭端与温度控制装置热连接。 温度控制装置加热和冷却通道中的热膨胀流体,其控制样品进入通道内和外通道的运动。
    • 3. 发明授权
    • Apparatus and methods for sample analysis
    • 仪器和样品分析方法
    • US06375817B1
    • 2002-04-23
    • US09293313
    • 1999-04-16
    • Todd A. TaylorWilliam W. CarsonLance Koutny
    • Todd A. TaylorWilliam W. CarsonLance Koutny
    • G01N2226
    • G01N27/44743B01L3/502784B01L2200/0605B01L2300/0816B01L2300/0861B01L2400/0415B01L2400/0487G01N27/44791Y10T436/2575
    • The present invention is directed to apparatus and methods for rapid, automated, microscale sample analysis using pressure differentials. The invention includes an apparatus having intersecting channels for introduction of a sample and separation of that sample into its components. The sample introduction and separation channels preferably are etched in a microfabricated device, such as a microchip, to form a junction. Pressure gradients are applied to the channels to form a sample plug in the separation channel. The separation channel may have disposed within it a medium for separation of the components suspected to be contained in the sample. For example, with the proper medium, a voltage gradient may be applied along the separation channel to separate the components of the sample electrophoretically. The apparatus also may include means for detecting the components of the sample subsequent to separation.
    • 本发明涉及使用压力差的快速,自动化,微量样品分析的装置和方法。 本发明包括具有用于引入样品和将样品分离成其组分的相交通道的装置。 样品引入和分离通道优选在诸如微芯片的微制造装置中蚀刻以形成结。 将压力梯度施加到通道以在分离通道中形成样品塞。 分离通道可以在其内设置有用于分离怀疑包含在样品中的组分的介质。 例如,使用适当的介质,可以沿着分离通道施加电压梯度以电泳分离样品的组分。 该装置还可以包括用于在分离之后检测样品的组分的装置。
    • 5. 发明授权
    • Method and system for examining the composition of a fluid or solid
sample using fluorescence and/or absorption spectroscopy
    • US5491344A
    • 1996-02-13
    • US160514
    • 1993-12-01
    • Jonathan E. KennyTodd A. Taylor
    • Jonathan E. KennyTodd A. Taylor
    • G01J3/14G01N21/31G01N21/64G01N30/74
    • G01N21/645G01J3/14G01N21/31G01N30/74
    • A method and system for examining the composition of a fluid or solid sample using fluorescence and/or absorption spectroscopy. In one embodiment, the system is adapted for use in examining liquid effluents as they elute from the end of a liquid chromatography column and comprises a Nd:YAG laser coupled to a harmonic generator. Pulses of the fourth harmonic therefrom are focused into a Raman shifter filled with a mixture of hydrogen and methane gases. The laser pulses have an intensity sufficient to produce an array of different-colored laser pulses by stimulated Raman scattering within the Raman shifter. These different-colored pulses are then dispersed according to their respective wavelengths and then launched into a plurality of optical fibers. The fibers tranmit the different-colored pulses to a specially-designed detection cell, where they simultaneously excite a flowing fluid sample contained within the cell at the same point of axial fluid flow. The fluid sample enters and exits the detection cell via tubes. Ultraviolet and visible lamp light is also used to illuminate the fluid sample, and the attenuation of this light is used to obtain an absorption spectrum of the sample. Optical fibers are used to transport fluorescent light, transmitted lamp light and a fraction of the Raman-shifted laser light to an imaging spectrograph. The light from each optical fiber is dispersed along a narrow strip by the spectrograph to produce an array of strips, each strip corresponding to one of the fibers, and is focused on the surface of a 2-dimensional CCD detector. The CCD detector converts each strip into electrical charges, which are digitized and processed by a computer to create an EEM. The aforementioned system is capable of obtaining an absorption spectrum from 200-479 nm with 0.5-5 nm spectral resolution and 10 fluorescence spectra simultaneously every 0.1-250 seconds for several hours, with crosstalk between channels of less than 10.sup.-4.