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1. 发明授权

US4747888A Amorphous soft magnetic thin film 失效
标题翻译：非晶软磁薄膜
公开(公告)号：US4747888A
公开(公告)日：1988-05-31
申请号：US829162
申请日：1986-02-14
申请人： Hiroshi Takino , Kiyonori Hayakawa , Kazuko Kawabata , Makoto Tsuruoka
发明人： Hiroshi Takino , Kiyonori Hayakawa , Kazuko Kawabata , Makoto Tsuruoka
IPC分类号： H01F10/16 , C22C19/07 , C22C45/04 , H01F1/153 , H01F10/12 , H01F10/13 , H01F1/04
CPC分类号： H01F1/15316 , H01F10/132 , H01F10/265 , Y10T428/12431
摘要： An improved alloy used in the form of an amorphous soft magnetic thin film having a desirable combination of saturation magnetic flux density and saturation magnetostriction constant, the alloy having the compositional formula:Co.sub.x Zr.sub.y Pd.sub.zwherein:0.85.ltoreq.x.ltoreq.0.940.04.ltoreq.y.ltoreq.0.070.01.ltoreq.z.ltoreq.0.10.
摘要翻译：一种改进的合金，以非晶软磁薄膜的形式使用，其具有饱和磁通密度和饱和磁致伸缩常数的理想组合，该合金具有组成式：CoxZryPdz其中：0.85

2. 发明授权

US4615748A Amorphous soft magnetic thin film 失效
标题翻译：非晶软磁薄膜
公开(公告)号：US4615748A
公开(公告)日：1986-10-07
申请号：US788140
申请日：1985-10-16
申请人： Hiroshi Takino , Kiyonori Hayakawa , Kazuko Kawabata , Makoto Tsuruoka
发明人： Hiroshi Takino , Kiyonori Hayakawa , Kazuko Kawabata , Makoto Tsuruoka
IPC分类号： H01F10/16 , C22C19/07 , C22C45/04 , H01F1/153 , H01F10/12 , H01F10/13 , C04B35/00
CPC分类号： H01F10/132 , H01F1/15316 , Y10T428/12431
摘要： An improved amorphous soft magnetic material particularly useful as a thin film for a magnetic recording and reproducing head. The amorphous material has the formula:Co.sub.1-x-y Hf.sub.x Pd.sub.ywherex is in the range from 0.04 to 0.08 andy is in the range from 0.005 to 0.15.The thin film is characterized by a high saturation magnetic flux density and a low saturation magnetostriction constant.
摘要翻译：特别用作磁记录和再现头的薄膜的改进的非晶软磁材料。无定形材料具有下式：Co1-x-yHfxPdy，其中x在0.04至0.08的范围内，y在0.005至0.15的范围内。该薄膜的特征在于高饱和磁通密度和低饱和磁致伸缩常数。

3. 发明授权

US6083740A System for purifying a polluted air by using algae 失效
标题翻译：使用藻类净化污染空气的系统
公开(公告)号：US6083740A
公开(公告)日：2000-07-04
申请号：US119607
申请日：1998-07-22
申请人： Keiun Kodo , Yasumasa Kodo , Makoto Tsuruoka
发明人： Keiun Kodo , Yasumasa Kodo , Makoto Tsuruoka
IPC分类号： B01D53/60 , B01D53/62 , B01D53/74 , B01D53/84 , B01J19/00
CPC分类号： B01D53/84
摘要： A system for purifying a polluted air by using algae such as Spirulina is capable of reducing carbon dioxide (CO.sub.2), nitrogen oxide (NO.sub.x) and/or sulfur oxide (SO.sub.x) in the polluted air and generating oxygen. That is, this system comprises a culture tank filled with a culture fluid including the algae, an air supply unit for forcing the polluted air into the culture fluid to dissolve carbon dioxide and nitrogen oxide and/or sulfur oxide in the culture fluid, and a lighting unit for radiating a light to the culture fluid. By radiating the light to the culture fluid in the presence of carbon dioxide, photosynthesis of the algae is promoted to convert carbon dioxide into oxygen. In addition, the algae use the nitrogen oxide and/or sulfur oxide as a nutrient during the photosynthesis. As a result, the present system can efficiently purify the polluted air to generate a purified air, which is rich in oxygen.
摘要翻译：通过使用诸如螺旋藻之类的藻类来净化污染空气的系统能够减少污染空气中的二氧化碳（CO 2），氮氧化物（NO x）和/或硫氧化物（SO x）并产生氧气。也就是说，该系统包括填充有包括藻类的培养液的培养槽，用于将污染空气强迫到培养液中以将培养液中的二氧化碳和氮氧化物和/或硫氧化物溶解的空气供给单元，以及用于向培养液照射光的照明单元。通过在存在二氧化碳的情况下将光照射到培养液中，促进藻类的光合作用以将二氧化碳转化为氧气。此外，藻类在光合作用期间使用氮氧化物和/或硫氧化物作为营养物。结果，本系统可以有效地净化污染空气，产生富氧的净化空气。

4. 发明授权

US5538849A Apparatus for automated assay of DNA probe and method for assaying nucleic acid in sample 失效
标题翻译：用于DNA探针自动化测定的装置和样品中核酸测定方法
公开(公告)号：US5538849A
公开(公告)日：1996-07-23
申请号：US174308
申请日：1993-12-29
申请人： Hiroaki Uematsu , Makoto Tsuruoka , Takashi Nakajima , Ken-ichi Chikanari , Misao Yoshimoto , Hiromichi Kobata
发明人： Hiroaki Uematsu , Makoto Tsuruoka , Takashi Nakajima , Ken-ichi Chikanari , Misao Yoshimoto , Hiromichi Kobata
IPC分类号： C12Q1/68 , G01N35/02 , C12N15/00 , G01N21/00 , G01N35/00
CPC分类号： G01N35/026 , C12Q1/6816 , Y10T436/11 , Y10T436/114165 , Y10T436/114998 , Y10T436/143333
摘要： An apparatus is presented for an automated assay of a DNA probe, which is performed by hybridizing a nucleic acid in a sample with a DNA probe marked with an enzyme and optically measuring a change that occurs in the substrate by catalysis of the enzyme which is bound with the DNA probe. The DNA probe hybridizes with the nucleic acid in the sample to assay the nucleic acid in the sample. Comprising (A) a sample-reagent unit, (B) a sample-reagent dispense unit, (C) a reaction vessel transport unit, (D) a hybridization unit, (E) a B/F separation unit, and (F) a light measurement unit; also presented is a method for assaying a nucleic acid in a sample by the apparatus of the present invention. According to the measurement apparatus of the present invention, a continuous and highly precise measurement is attainable. In particular, the light-shielding structure of the light measurement unit exhibits high levels of light-shielding effect and contributes to efficient light measurement and prevention of degradation of light receiving elements.
摘要翻译：提供了一种用于DNA探针的自动测定的装置，其通过将样品中的核酸与标记有酶的DNA探针杂交并通过催化结合的酶光学测量在底物中发生的变化来进行与DNA探针。 DNA探针与样品中的核酸杂交以测定样品中的核酸。包括（A）样品试剂单元，（B）样品试剂分配单元，（C）反应容器输送单元，（D）杂交单元，（E）B / F分离单元和（F）光测量单元; 还提出了通过本发明的装置测定样品中的核酸的方法。根据本发明的测量装置，可以获得连续高精度的测量。特别地，光测量单元的遮光结构具有高水平的遮光效果，并且有助于有效的光测量和防止光接收元件的劣化。

5. 发明授权

US06329142B2 Assay of nucleic acid by fluorescence polarization technique and detection of verotoxin-producing microorganisms 有权
标题翻译：通过荧光偏振技术测定核酸并检测产生毒素的微生物
公开(公告)号：US06329142B2
公开(公告)日：2001-12-11
申请号：US09127864
申请日：1998-08-03
申请人： Makoto Tsuruoka , Isao Karube
发明人： Makoto Tsuruoka , Isao Karube
IPC分类号： C12Q168
CPC分类号： C12Q1/686 , C12Q2561/119 , C12Q2531/107
摘要： A method for assaying a nucleic acid comprising amplifying a nucleic acid in a sample by gene amplification and measuring the increased amount of the nucleic acid by a fluorescence polarization technique, in which the gene amplification is carried out by asymmetric amplification, or annealing with the primers used in the amplification is carried out after amplification of the nucleic acid, thereby to facilitate binding of a fluorescence-labeled reagent to the target single-stranded nucleic acid.
摘要翻译：一种测定核酸的方法，包括通过基因扩增扩增样品中的核酸，并通过荧光偏振技术测量增加的核酸量，其中通过不对称扩增进行基因扩增或用引物退火用于扩增的核酸在扩增后进行，从而促进荧光标记的试剂与目标单链核酸的结合。

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