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    • 2. 发明授权
    • Bioassay substrate and bioassay device and method
    • 生物测定底物和生物测定装置及方法
    • US07718129B2
    • 2010-05-18
    • US10559745
    • 2004-06-10
    • Takayoshi MamineYasuhiro SakamotoMotohiro FurukiIsamu Nakao
    • Takayoshi MamineYasuhiro SakamotoMotohiro FurukiIsamu Nakao
    • G01N21/00
    • G01N21/6452G01N21/6428G01N33/582G01N35/00069G01N2021/6482
    • A bioassay substrate (1) takes a flat-plate shape in which the principal surface similar to that of optical disc such as CD, etc. is circular. At the center of the substrate (1), there is formed a center hole (2) into which a chucking mechanism for rotation and holding is inserted. The substrate (1) is rotationally driven with the center hole (2) being as center. On the substrate (1), there are formed two regions of a recording region (3) and a reaction region (4) which are formed in concentrical form in a radial direction. The recording region (3) is a region where, similarly to the optical disk information recording medium, laser beams are irradiated so that recording/reproduction of information is optically performed. The reaction region (4) is a region serving as the filed of mutual reaction between probe DNA (nucleotide chain for detection) and sample DNA (marked or labeled nucleotide chain), in concrete terms, the field of hybridization reaction.
    • 生物测定基板(1)采用平板形状,其中与诸如CD等的光盘类似的主表面是圆形的。 在基板(1)的中心形成有中心孔(2),插入有用于旋转和保持的夹紧机构。 基板(1)以中心孔(2)为中心旋转驱动。 在基板(1)上形成有径向形成为同心圆形的记录区域(3)和反应区域(4)的两个区域。 记录区域(3)是类似于光盘信息记录介质照射激光束以便光学地执行信息的记录/再现的区域。 反应区(4)是用作探针DNA(检测用核苷酸)与样品DNA(标记或标记核苷酸链)之间相互反应的领域的区域,具体来说是杂交反应场。
    • 3. 发明申请
    • Bioassay substrate and bioassay device and method
    • 生物测定底物和生物测定装置及方法
    • US20060128030A1
    • 2006-06-15
    • US10559745
    • 2004-06-10
    • Takayoshi MamineYasuhiro SakamotoMotohiro FurukiIsamu Nakao
    • Takayoshi MamineYasuhiro SakamotoMotohiro FurukiIsamu Nakao
    • G01N33/543C12M1/34
    • G01N21/6452G01N21/6428G01N33/582G01N35/00069G01N2021/6482
    • A bioassay substrate (1) takes a flat-plate shape in which the principal surface similar to that of optical disc such as CD, etc. is circular. At the center of the substrate (1), there is formed a center hole (2) into which a chucking mechanism for rotation and holding is inserted. The substrate (1) is rotationally driven with the center hole (2) being as center. On the substrate (1), there are formed two regions of a recording region (3) and a reaction region (4) which are formed in concentrical form in a radial direction. The recording region (3) is a region where, similarly to the optical disk information recording medium, laser beams are irradiated so that recording/reproduction of information is optically performed. The reaction region (4) is a region serving as the filed of mutual reaction between probe DNA (nucleotide chain for detection) and sample DNA (marked or labeld nucleotide chain), in concrete terms, the field of hybridization reaction.
    • 生物测定基板(1)采用平板形状,其中与诸如CD等的光盘类似的主表面是圆形的。 在基板(1)的中心形成有中心孔(2),插入有用于旋转和保持的夹紧机构。 基板(1)以中心孔(2)为中心旋转驱动。 在基板(1)上形成有径向形成为同心圆形的记录区域(3)和反应区域(4)的两个区域。 记录区域(3)是类似于光盘信息记录介质照射激光束以便光学地执行信息的记录/再现的区域。 反应区域(4)是用作探针DNA(检测用核苷酸链)和样品DNA(标记或者标记的核苷酸链)之间相互作用的区域的区域,具体来说是杂交反应场。
    • 7. 发明申请
    • Interaction detecting method and bioassay device, and bioassay-use substrate
    • 相互作用检测方法和生物测定装置以及生物测定用底物
    • US20060063153A1
    • 2006-03-23
    • US10529949
    • 2003-09-24
    • Takayoshi MamineTakashi Kinoshita
    • Takayoshi MamineTakashi Kinoshita
    • C12Q1/68C12M1/34
    • G01N29/036B82Y5/00C12Q1/6816G01N2291/0257C12Q2565/60
    • In a cell detecting part (2), and end face (13a) of a cantilever (13) is previously surface treated so that a detecting nucleotide chain D can be fixed thereto. In a reaction area (10), and electric field is generated by a cathode (11) and an anode (12). A target nucleotide chain T dripped from a nozzle (3) moves to the end face (13a) while the target nucleotide chain T is stretched. When the detecting nucleotide chain D and the target nucleotide chain T are hybridized, the mass of the cantilever (13) is increased to lower a natural frequency. Thus, ac voltage is applied to the cantilever (13) to measure the change of the natural frequency. Thus, whether or not there is the hybridization is detected and the number of the hybridized target nucleotide chains T is quantitatively detected.
    • 在细胞检测部(2)中,预先对悬臂(13)的端面(13a)进行表面处理,使检测用核苷酸链D固定于其上。 在反应区域(10)中,由阴极(11)和阳极(12)产生电场。 从喷嘴(3)滴下的目标核苷酸链T移动到端面(13a),同时靶核苷酸链T被拉伸。 当检测核苷酸链D和靶核苷酸链T杂交时,悬臂(13)的质量增加以降低固有频率。 因此,将交流电压施加到悬臂(13)以测量固有频率的变化。 因此,是否检测到杂交,并且定量检测杂交的靶核苷酸链T的数量。
    • 8. 发明授权
    • Semiconductor manufacturing apparatus and semiconductor device manufacturing method
    • 半导体制造装置及半导体装置的制造方法
    • US06549608B1
    • 2003-04-15
    • US09538737
    • 2000-03-30
    • Takayoshi MamineNobuyuki MatsuzawaNoriyuki Kishii
    • Takayoshi MamineNobuyuki MatsuzawaNoriyuki Kishii
    • G21K500
    • G03F7/70008
    • To provide a semiconductor manufacturing apparatus and a semiconductor device manufacturing method able to form a sufficiently precise pattern by ablation. A semiconductor manufacturing apparatus comprising a light source emitting light of a first wavelength on the surface of a wafer and a mask through which at least a part of the light of the first wavelength passes and removing a material of the part of the wafer exposed by the light of the first wavelength by vaporization, wherein the light source comprises an electron beam generating means for generating an electron beam and a light emitting means for emitting light of a second wavelength longer than the first wavelength and wherein the light of the first wavelength is inverse Compton scattered light obtained by collision of electrons in the electron beam with photons in the light of the second wavelength causing the energy of the electrons to be given to the photons and a semiconductor device manufacturing method using the apparatus.
    • 1.一种半导体制造装置,其特征在于,具有通过烧蚀形成足够精细的图案的半导体制造装置和半导体装置的制造方法。1。一种半导体制造装置,其特征在于,包括在晶片表面上发射第一波长的光的光源和至少一个 第一波长的光的一部分通过蒸发而通过并除去由第一波长的光曝光的晶片的部分的材料,其中光源包括用于产生电子束的电子束产生装置和发光装置 用于发射比第一波长长的第二波长的光,其中第一波长的光是通过电子束中的电子与第二波长的光子碰撞而获得的康普顿散射光,导致电子的能量 给予光子和使用该设备的半导体器件制造方法 s。