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1. 发明授权

US08178450B2 TiO2-containing silica glass and optical member for EUV lithography using high energy densities as well as special temperature controlled process for its manufacture 失效
标题翻译：含TiO 2的石英玻璃和用于EUV光刻的光学构件，使用高能量密度以及用于其制造的特殊温度控制方法
公开(公告)号：US08178450B2
公开(公告)日：2012-05-15
申请号：US12868900
申请日：2010-08-26
申请人： Akio Koike , Kenta Saito , Long Shao , Yasutomi Iwahashi , Shinya Kikugawa
发明人： Akio Koike , Kenta Saito , Long Shao , Yasutomi Iwahashi , Shinya Kikugawa
IPC分类号： C03C3/06 , C03C3/04 , C03B37/018
CPC分类号： C03B19/1453 , C03B19/1415 , C03B2201/075 , C03B2201/23 , C03B2201/42 , C03B2207/70 , C03B2207/81 , C03C3/06 , C03C3/076 , C03C2201/23 , C03C2201/42 , C03C2203/44 , C03C2203/52 , C03C2203/54 , Y02P40/57
摘要： The present invention provides a TiO2—SiO2 glass whose coefficient of linear thermal expansion in the range of the time of irradiation with EUV light is substantially zero when used as an optical member of an exposure tool for EUVL and which has extremely high surface smoothness. The present invention relates to a TiO2-containing silica glass having a TiO2 content of from 7.5 to 12% by mass, a temperature at which a coefficient of linear thermal expansion is 0 ppb/° C., falling within the range of from 40 to 110° C., and a standard deviation (σ) of a stress level of striae of 0.03 MPa or lower within an area of 30 mm×30 mm in at least one plane.
摘要翻译：本发明提供一种TiO 2 -SiO 2玻璃，当用作EUVL的曝光工具的光学部件并且具有非常高的表面光滑度时，在EUV光的照射时间范围内的线性热膨胀系数基本上为零。本发明涉及TiO 2含量为7.5〜12质量％，线膨胀系数为0ppb /℃的温度，在40〜 110℃，在至少一个平面内在30mm×30mm的区域内的条纹应力水平为0.03MPa以下的标准偏差（＆sgr）。

2. 发明申请

US20100323871A1 TIO2-CONTAINING SILICA GLASS AND OPTICAL MEMBER FOR EUV LITHOGRAPHY USING HIGH ENERGY DENSITIES AS WELL AS SPECIAL TEMPERATURE CONTROLLED PROCESS FOR ITS MANUFACTURE 失效
标题翻译：含氧二氧化硅玻璃和光学成员，用于使用高能量密度的EUV光刻作为其特殊温度控制过程的制造
公开(公告)号：US20100323871A1
公开(公告)日：2010-12-23
申请号：US12868900
申请日：2010-08-26
申请人： Akio Koike , Kenta Saito , Long Shao , Yasutomi Iwahashi , Shinya Kikugawa
发明人： Akio Koike , Kenta Saito , Long Shao , Yasutomi Iwahashi , Shinya Kikugawa
IPC分类号： C03C3/04
CPC分类号： C03B19/1453 , C03B19/1415 , C03B2201/075 , C03B2201/23 , C03B2201/42 , C03B2207/70 , C03B2207/81 , C03C3/06 , C03C3/076 , C03C2201/23 , C03C2201/42 , C03C2203/44 , C03C2203/52 , C03C2203/54 , Y02P40/57
摘要： The present invention provides a TiO2—SiO2 glass whose coefficient of linear thermal expansion in the range of the time of irradiation with EUV light is substantially zero when used as an optical member of an exposure tool for EUVL and which has extremely high surface smoothness. The present invention relates to a TiO2-containing silica glass having a TiO2 content of from 7.5 to 12% by mass, a temperature at which a coefficient of linear thermal expansion is 0 ppb/° C., falling within the range of from 40 to 110° C., and a standard deviation (σ) of a stress level of striae of 0.03 MPa or lower within an area of 30 mm×30 mm in at least one plane.
摘要翻译：本发明提供一种TiO 2 -SiO 2玻璃，当用作EUVL的曝光工具的光学部件并且具有非常高的表面光滑度时，在EUV光的照射时间范围内的线性热膨胀系数基本上为零。本发明涉及TiO 2含量为7.5〜12质量％，线膨胀系数为0ppb /℃的温度，在40〜 110℃，在至少一个平面内在30mm×30mm的区域内的条纹应力水平为0.03MPa以下的标准偏差（＆sgr）。

3. 发明申请

US20070292909A1 Fluorescent Protein 有权
标题翻译：荧光蛋白
公开(公告)号：US20070292909A1
公开(公告)日：2007-12-20
申请号：US10581551
申请日：2004-12-03
申请人： Atsushi Miyawaki , Takako Kogure , Hiroshi Hama , Masataka Kinjo , Kenta Saito , Satoshi Karasawa , Toshio Araki
发明人： Atsushi Miyawaki , Takako Kogure , Hiroshi Hama , Masataka Kinjo , Kenta Saito , Satoshi Karasawa , Toshio Araki
IPC分类号： C07H21/04 , C07K14/00 , C12N15/00 , C12Q1/02
CPC分类号： C07K14/37 , C07K14/43504 , G01N33/533
摘要： An object of the present invention is to provide a red or orange fluorescent protein, which is characterized in that the difference (stokes shift) between an excitation peak value (wavelength of maximum absorption) and a fluorescence peak value (wavelength of maximum fluorescence) is greatened, so that the maximum fluorescence can be obtained by the maximum excitation. The present invention provides a novel fluorescent protein monomerized by introducing a mutation into a florescent protein derived from Fungia sp., and a novel chromoprotein and fluorescent protein derived from Montipora. sp.
摘要翻译：本发明的目的是提供一种红色或橙色荧光蛋白，其特征在于，激发峰值（最大吸收波长）与荧光峰值（最大荧光的波长）之间的差异（斯托克斯偏移）为从而可以通过最大激发获得最大荧光。本发明提供了一种新颖的荧光蛋白，其通过将突变引入到来自真菌属的荧光蛋白中而单体化，以及衍生自Montipora的新型生色蛋白和荧光蛋白。 sp。

4. 发明申请

US20090253217A1 Method of Quickly Detecting Antigen Using Fluorescence Correlation Spectroscopy or Fluorescence Cross-Correlation Spectroscopy 审中-公开
标题翻译：使用荧光相关光谱或荧光相关光谱快速检测抗原的方法
公开(公告)号：US20090253217A1
公开(公告)日：2009-10-08
申请号：US12066284
申请日：2006-09-08
申请人： Kenta Saito , Hiroshi Sakata , Fumihiko Fujii , Masataka Kinjo , Mamoru Tamura
发明人： Kenta Saito , Hiroshi Sakata , Fumihiko Fujii , Masataka Kinjo , Mamoru Tamura
IPC分类号： G01N33/566
CPC分类号： G01N33/536 , G01N33/582 , G01N33/6896 , G01N2021/6439 , G01N2800/2828
摘要： The present invention is to provide a method of quickly detecting an antigen at an arbitrary concentration in an antigen sample, without a multi-stage examination of the concentration ratio between a detection reagent and an antigen to be detected, particularly when the concentration of the antigen in the sample is unknown, in the method of detecting an antigen using fluorescence correlation spectroscopy (FCS) or fluorescence cross-correlation spectroscopy (FCCS). By preparing (1) a series to which only a detection reagent is added and (2) a series to which an antigen and the detection reagent are added to achieve a maximum trimer concentration, and by performing a fluorescence spectroscopic analysis, the presence or absence of the antigen in the detection sample is quickly detected by the presence or absence of a trimer detection signal from a detector in the cases of (1) and (2), in a method of detecting an antigen by FCS or FCCS using as a detection reagent a fluorescent-labeled intact antibody or fluorescent-labeled antibody fragment targeted to an epitope of the antigen to be detected, and a non-fluorescent-labeled intact antibody or fluorescent-labeled intact antibody or fluorescent-labeled antibody fragment targeted to another epitope of the antigen.
摘要翻译：本发明提供一种在抗原样品中以任意浓度快速检测抗原的方法，而不需要对检测试剂和待检测抗原之间的浓度比进行多阶段检查，特别是当抗原浓度在样品中，在使用荧光相关光谱法（FCS）或荧光相关光谱法（FCCS）检测抗原的方法中是未知的。通过制备（1）仅添加检测试剂的系列和（2）添加抗原和检测试剂以达到最大三聚体浓度的一系列序列，通过进行荧光光谱分析，存在或不存在在（1）和（2）的情况下，通过检测器的三聚体检测信号的存在或不存在，通过FCS或FCCS检测抗原的方法来检测检测样品中的抗原，试剂荧光标记的完整抗体或靶向要检测的抗原表位的荧光标记的抗体片段，以及靶向另一表位的非荧光标记的完整抗体或荧光标记的完整抗体或荧光标记的抗体片段抗原。

5. 发明申请

US20120034643A1 FLUORESCENT PROTEIN 有权
标题翻译：荧光蛋白
公开(公告)号：US20120034643A1
公开(公告)日：2012-02-09
申请号：US13196499
申请日：2011-08-02
申请人： Atsushi MIYAWAKI , Takako KOGURE , Hiroshi HAMA , Masataka KINJO , Kenta SAITO , Satoshi KARASAWA , Toshio ARAKI
发明人： Atsushi MIYAWAKI , Takako KOGURE , Hiroshi HAMA , Masataka KINJO , Kenta SAITO , Satoshi KARASAWA , Toshio ARAKI
IPC分类号： C12Q1/02 , C12N15/12 , C12N15/63 , C12N5/10 , C12N1/21 , C12N1/19 , C12N1/15 , C07K14/435 , C07K19/00
CPC分类号： C07K14/37 , C07K14/43504 , G01N33/533
摘要： An object of the present invention is to provide a red or orange fluorescent protein, which is characterized in that the difference (stokes shift) between an excitation peak value (wavelength of maximum absorption) and a fluorescence peak value (wavelength of maximum fluorescence) is greatened, so that the maximum fluorescence can be obtained by the maximum excitation. The present invention provides a novel fluorescent protein monomerized by introducing a mutation into a florescent protein derived from Fungia sp., and a novel chromoprotein and fluorescent protein derived from Montipora. sp.
摘要翻译：本发明的目的是提供一种红色或橙色荧光蛋白，其特征在于，激发峰值（最大吸收波长）与荧光峰值（最大荧光的波长）之间的差异（斯托克斯偏移）为从而可以通过最大激发获得最大荧光。本发明提供了一种新颖的荧光蛋白，其通过将突变引入到来自真菌属的荧光蛋白中而单体化，以及衍生自Montipora的新型生色蛋白和荧光蛋白。 sp。

6. 发明申请

US20080127679A1 PROCESS FOR PRODUCING ALKALI FREE GLASS AND ALKALI FREE GLASS PLATE 审中-公开
公开(公告)号：US20080127679A1
公开(公告)日：2008-06-05
申请号：US11969532
申请日：2008-01-04
申请人： Manabu Nishizawa , Junichiro Kase , Kenta Saito , Kei Maeda , Syuji Matsumoto
发明人： Manabu Nishizawa , Junichiro Kase , Kenta Saito , Kei Maeda , Syuji Matsumoto
IPC分类号： C03B5/225 , C03C3/091
CPC分类号： C03B5/225 , C03B5/2252 , C03C1/004 , C03C3/091 , Y02P40/57
摘要： To provide a process for producing and alkali free glass for effectively suppressing bubbles, and an alkali free glass produced by the process, which is suitable as a glass substrate for flat panel displays and has few bubbles.A process for producing an alkali free glass containing substantially no alkali metal oxide, which comprises melting a glass starting material having a matrix composition of the following composition, and subjecting the molten glass to a treatment process of removing bubbles under reduced pressure, stirring or transferring under a condition where the molten glass is in contact with a platinum member, wherein the starting material is prepared so as to contain SnO2 in an amount of from 0.01 to 2.0% per 100% of the total amount of the above matrix composition; the starting material is melted under heating at from 1,500 to 1,650° C.; then bubbles contained in the molten glass are permitted to rise to the surface of the molten glass, together with oxygen bubbles generated by a reduction reaction in which SnO2 in the molten glass is reduced to SnO; and in the above treatment process, the oxygen bubbles generated at the interface between the molten glass and the platinum member are permitted to be absorbed by an oxidation reaction in which SnO is oxidized to SnO2, under a condition where the molten glass is from 1,300 to 1,500° C.Composition as represented by the mass percentage: SiO258.4 to 66.0%, Al2O315.3 to 22.0%, B2O3 5.0 to 12.0%, MgO 0 to 6.5%, CaO 0 to 7.0%, SrO 4 to 12.5%, BaO 0 to 2.0%, MgO + CaO + SrO + BaO 9.0 to 18.0%.

7. 发明授权

US08420781B2 Fluorescent protein 有权
标题翻译：荧光蛋白
公开(公告)号：US08420781B2
公开(公告)日：2013-04-16
申请号：US13196499
申请日：2011-08-02
申请人： Atsushi Miyawaki , Takako Kogure , Hiroshi Hama , Masataka Kinjo , Kenta Saito , Satoshi Karasawa , Toshio Araki
发明人： Atsushi Miyawaki , Takako Kogure , Hiroshi Hama , Masataka Kinjo , Kenta Saito , Satoshi Karasawa , Toshio Araki
IPC分类号： C07K1/00 , C08B37/08
CPC分类号： C07K14/37 , C07K14/43504 , G01N33/533
摘要： An object of the present invention is to provide a red or orange fluorescent protein, which is characterized in that the difference (stokes shift) between an excitation peak value (wavelength of maximum absorption) and a fluorescence peak value (wavelength of maximum fluorescence) is greatened, so that the maximum fluorescence can be obtained by the maximum excitation. The present invention provides a novel fluorescent protein monomerized by introducing a mutation into a florescent protein derived from Fungia sp., and a novel chromoprotein and fluorescent protein derived from Montipora. sp.
摘要翻译：本发明的目的是提供一种红色或橙色荧光蛋白，其特征在于，激发峰值（最大吸收波长）与荧光峰值（最大荧光的波长）之间的差异（斯托克斯偏移）为从而可以通过最大激发获得最大荧光。本发明提供了一种新颖的荧光蛋白，其通过将突变引入到来自真菌属的荧光蛋白中而单体化，以及衍生自Montipora的新型生色蛋白和荧光蛋白。 sp。

8. 发明授权

US08017746B2 Fluorescent protein 有权
标题翻译：荧光蛋白
公开(公告)号：US08017746B2
公开(公告)日：2011-09-13
申请号：US10581551
申请日：2004-12-03
申请人： Atsushi Miyawaki , Takako Kogure , Hiroshi Hama , Masataka Kinjo , Kenta Saito , Satoshi Karasawa , Toshio Araki
发明人： Atsushi Miyawaki , Takako Kogure , Hiroshi Hama , Masataka Kinjo , Kenta Saito , Satoshi Karasawa , Toshio Araki
IPC分类号： C07H21/02 , C12Q1/02 , C12N1/20
CPC分类号： C07K14/37 , C07K14/43504 , G01N33/533
摘要： An object of the present invention is to provide a red or orange fluorescent protein, which is characterized in that the difference (stokes shift) between an excitation peak value (wavelength of maximum absorption) and a fluorescence peak value (wavelength of maximum fluorescence) is greatened, so that the maximum fluorescence can be obtained by the maximum excitation. The present invention provides a novel fluorescent protein monomerized by introducing a mutation into a florescent protein derived from Fungia sp., and a novel chromoprotein and fluorescent protein derived from Montipora. sp.
摘要翻译：本发明的目的是提供一种红色或橙色荧光蛋白，其特征在于，激发峰值（最大吸收波长）与荧光峰值（最大荧光的波长）之间的差异（斯托克斯偏移）为从而可以通过最大激发获得最大荧光。本发明提供了一种新颖的荧光蛋白，其通过将突变引入到来自真菌属的荧光蛋白中而单体化，以及衍生自Montipora的新型生色蛋白和荧光蛋白。 sp。

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