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    • 2. 发明授权
    • Calibration method and apparatus for optical scanner
    • 光学扫描仪的校准方法和装置
    • US5689110A
    • 1997-11-18
    • US670540
    • 1996-06-27
    • Louis J. DietzThomas M. Baer
    • Louis J. DietzThomas M. Baer
    • G01N21/64G01J3/28G01N15/10G01N21/27G01J3/443
    • G01N15/1012G01N21/274G01J2003/2866
    • A calibration method and device for a fluorescence spectrometer which uses fluorescence from a homogeneous solid state standard as the source of calibration fluorescence and wherein the solid state standard may be built into the optical scanner and the calibration may be automatically performed as a routine step when using the optical scanner. A gold standard establishes fluorescent units, and the fluorescence spectrometer is calibrated by reference to calibration standards, such as calibration rubies, which are themselves rated against the gold standard and built into the fluorescence spectrometer to provide an unchanging reference to the gold standard and by which simultaneous calibration of two or more channels of a multi-channel fluorescence spectrometer may be accomplished, including automatically calibrating a multi-channel optical scanner when it is turned on to achieve an acceptable level of sensitivity in each channel and to adjust for any relative shift in sensitivity between the channels.
    • 用于荧光光谱仪的校准方法和装置,其使用来自均匀固态标准的荧光作为校准荧光源,并且其中固态标准可内置在光学扫描仪中,并且可以在使用时自动执行校准作为常规步骤 光学扫描仪。 黄金标准建立荧光单位,并且通过参考校准标准校准红宝石来校准荧光光谱仪,例如校准红宝石,其自身被评定为黄金标准,并被内置于荧光光谱仪中以提供对黄金标准的不变参考,并且由此 可以实现多通道荧光光谱仪的两个或更多个通道的同时校准,包括当其打开时自动校准多通道光学扫描仪以在每个通道中实现可接受的灵敏度水平并且调整任何相对偏移 通道之间的灵敏度。
    • 3. 发明授权
    • Laser microdissection apparatus and method
    • 激光显微解剖设备及方法
    • US08715955B2
    • 2014-05-06
    • US11222281
    • 2005-09-08
    • Brian W. DonovanThomas M. Baer
    • Brian W. DonovanThomas M. Baer
    • G01N1/28
    • G01N1/28G01N1/2813G01N1/286G01N1/30G01N1/44G01N2001/2826G01N2001/2833G01N2001/284G01N2001/2886Y10T156/10Y10T156/1054
    • Systems and methods for automated laser microdissection are disclosed. In one variation, targeted biological material is manually or automatically selected and a transfer film is placed in juxtaposition to the location of an interior of a cut path. In another variation, a sample of biological material is mounted onto a polymer membrane which is then placed onto a substrate. Targeted biological material is manually or automatically selected and a transfer film is placed in juxtaposition with the targeted biological material on the side of the biological material. In yet another variation, a sample of biological material is mounted onto a polymer membrane which is then inverted onto a substrate. Targeted biological material is manually or automatically selected and a transfer film is placed in juxtaposition with the targeted biological material on the side of the polymer membrane. Then, an UV laser cuts along a cut path around the targeted portions of biological material in a closed cut path or a substantially closed cut path defining an interior and an exterior portion of the tissue sample. In a substantially closed cut path, bridges are left spanning the interior of the cut path and the exterior of the cut path. An IR laser activates at least a portion of the transfer film such that the transfer film in the vicinity of targeted portion adheres to the biological material interior to the cut path. The transfer film is then removed separating the targeted portions of biological material which are adhered to the transfer film from the remaining portion of the tissue sample.
    • 公开了用于自动激光显微切割的系统和方法。 在一个变型中,手动或自动选择目标生物材料,并且将转移膜并排放置在切割路径的内部的位置。 在另一个变体中,将生物材料样品安装在聚合物膜上,然后将其放置在基底上。 手动或自动选择靶向生物材料,并将转移膜与生物材料侧面上的靶向生物材料并置放置。 在另一个变体中,将生物材料样品安装在聚合物膜上,然后将其反转到基底上。 手动或自动选择目标生物材料,并将转移膜与聚合物膜侧面上的目标生物材料并置放置。 然后,UV激光沿着围绕生物材料的目标部分的切割路径沿封闭的切割路径或限定组织样本的内部和外部部分的基本封闭的切割路径切割。 在基本封闭的切割路径中,跨越切割路径的内部和切割路径的外部。 红外激光激活转印膜的至少一部分,使得目标部分附近的转印膜附着在生物材料内部至切割路径。 然后除去转移膜,从生物材料的目标部分分离出粘附到转移膜上的剩余部分的组织样品。