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    • 2. 发明授权
    • Methods for the cryopreservation of cells
    • 细胞冷冻保存方法
    • US09538745B2
    • 2017-01-10
    • US12226300
    • 2007-04-12
    • Xiaoming HeThomas L. TothMehmet TonerJon Edd
    • Xiaoming HeThomas L. TothMehmet TonerJon Edd
    • A01N1/02
    • A01N1/02A01N1/0221A01N1/0268A01N1/0278
    • The present invention features novel methods for the cryopreservation of mammalian cell that combine the advantages of the slow-freezing and vitrification approaches while avoiding their shortcomings. Generally, the methods include the use of a capillary tube made of a thermally conductive wall material and a thin wall such that the ratio of the thermal conductivity of the wall material to the wall thickness is at least 1,000-500,000. The solution is then exposed to temperatures equal to or less than −80° C. and the vitrification solution containing the mammalian cells is cooled at a rate equal to or greater than 30,000-100,000,000° C./minute. The exposure of the capillary tube with a thermally conductive and thin wall allows for vitrification of the solution in the absence of ice formation. Cryoprotectants can also be added to the vitrification solution to further prevent ice formation.
    • 本发明的特征在于用于冷冻保存哺乳动物细胞的新方法,其结合了缓慢冷冻和玻璃化方法的优点,同时避免了它们的缺点。 通常,这些方法包括使用由导热壁材料制成的毛细管和薄壁,使得壁材料的导热率与壁厚之比至少为1,000-500,000。 然后将溶液暴露于等于或小于-80℃的温度,并将含有哺乳动物细胞的玻璃化溶液以等于或大于30,000-10000,000℃/分钟的速率冷却。 毛细管与导热和薄壁的接触允许在没有冰层形成的情况下玻璃化溶液。 也可以将冷冻保护剂加入到玻璃化溶液中以进一步防止冰层形成。
    • 3. 发明申请
    • Methods for the Cryopreservation of Mammalian Cells
    • 哺乳动物细胞冷冻保存方法
    • US20090305224A1
    • 2009-12-10
    • US12226300
    • 2007-04-12
    • Xiaoming HeThomas L. TothMehmet TonerJon Edd
    • Xiaoming HeThomas L. TothMehmet TonerJon Edd
    • A01N1/02C12N5/02
    • A01N1/02A01N1/0221A01N1/0268A01N1/0278
    • The present invention features novel methods for the cryopreservation of mammalian cell that combine the advantages of the slow-freezing and vitrification approaches while avoiding their shortcomings. Generally, the methods include the use of a capillary tube made of a thermally conductive wall material and a thin wall such that the ratio of the thermal conductivity of the wall material to the wall thickness is at least 1,000-500,000. The solution is then exposed to temperatures equal to or less than −80° C. and the vitrification solution containing the mammalian cells is cooled at a rate equal to or greater than 30,000-100,000,000° C./minute. The exposure of the capillary tube with a thermally conductive and thin wall allows for vitrification of the solution in the absence of ice formation. Cryoprotectants can also be added to the vitrification solution to further prevent ice formation.
    • 本发明的特征在于用于冷冻保存哺乳动物细胞的新方法,其结合了缓慢冷冻和玻璃化方法的优点,同时避免了它们的缺点。 通常,这些方法包括使用由导热壁材料制成的毛细管和薄壁,使得壁材料的导热率与壁厚之比至少为1,000-500,000。 然后将溶液暴露于等于或小于-80℃的温度,并将含有哺乳动物细胞的玻璃化溶液以等于或大于30,000-10000,000℃/分钟的速率冷却。 毛细管与导热和薄壁的接触允许在没有冰层形成的情况下玻璃化溶液。 也可以将冷冻保护剂加入到玻璃化溶液中以进一步防止冰层形成。
    • 7. 发明授权
    • Methods and apparatus for calibrating CT x-ray beam tracking loop
    • 用于校准CT X射线束跟踪循环的方法和装置
    • US06310938B1
    • 2001-10-30
    • US09384937
    • 1999-08-27
    • Thomas L. TothGeorge E. SeidenschnurNeil B. Bromberg
    • Thomas L. TothGeorge E. SeidenschnurNeil B. Bromberg
    • G21K100
    • A61B6/583A61B6/4021G01N23/046G01N2223/419G01N2223/612
    • The present invention is, in one embodiment, a method for determining tracking control parameters for positioning an x-ray beam of a computed tomography imaging system having a movable collimator positionable in steps and a detector array including a plurality of rows of detector elements. The method includes steps of obtaining detector samples at a series of collimator step positions while determining a position of a focal spot of the x-ray beam; determining a beam position for each detector element at each collimator step utilizing the determined focal spot positions, a nominal focal spot length, and geometric parameters of the x-ray beam, collimator, and detector array; and determining a calibration parameter utilizing information so obtained. For example, in determining a target beam position at which to maintain the x-ray beam, a detector element differential error is determined according to ratios of successive collimator step positions; and a target beam position is selected for an isocenter element in accordance with the determined element differential errors.
    • 本发明在一个实施例中是一种用于确定跟踪控制参数的方法,所述跟踪控制参数用于定位具有可定位的可移动准直器的计算机断层摄影成像系统的X射线束和包括多行检测器元件的检测器阵列。 该方法包括以下步骤:在确定X射线束的焦斑的位置的同时在一系列准直器步骤位置获得检测器样本; 使用所确定的焦点位置,标称焦点长度以及x射线束,准直仪和检测器阵列的几何参数来确定每个准直器步骤处的每个检测器元件的光束位置; 以及使用如此获得的信息来确定校准参数。 例如,在确定维持X射线束的目标光束位置时,根据连续的准直仪台阶位置的比例来确定检测器元件差分误差; 并且根据确定的元件微分误差为等角点元件选择目标光束位置。