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    • 4. 发明申请
    • Methods of producing carbon nanotubes using peptide or nucleic acid micropatterning
    • 使用肽或核酸微图案生产碳纳米管的方法
    • US20090170725A1
    • 2009-07-02
    • US11344713
    • 2006-01-31
    • Mineo YamakawaYuegang ZhangXing SuLei SunAndrew A. BerlinNarayanan Sundararajan
    • Mineo YamakawaYuegang ZhangXing SuLei SunAndrew A. BerlinNarayanan Sundararajan
    • C40B40/08B82B1/00
    • B82Y40/00B82Y10/00B82Y30/00C01B32/162C01B2202/08C01B2202/36D01F9/127H01L51/0048H01L51/0052
    • The methods, apparatus and systems disclosed herein concern ordered arrays of carbon nanotubes. In particular embodiments of the invention, the nanotube arrays are formed by a method comprising attaching catalyst nanoparticles 140, 230 to polymer 120, 210 molecules, attaching the polymer 120, 210 molecules to a substrate, removing the polymer 120, 210 molecules and producing carbon nanotubes on the catalyst nanoparticles 140, 230. The polymer 120, 210 molecules can be attached to the substrate in ordered patterns, using self-assembly or molecular alignment techniques. The nanotube arrays can be attached to selected areas 110, 310 of the substrate. Within the selected areas 110, 310, the nanotubes are distributed non-randomly. Other embodiments disclosed herein concern apparatus that include ordered arrays of nanotubes attached to a substrate and systems that include ordered arrays of carbon nanotubes attached to a substrate, produced by the claimed methods. In certain embodiments, provided herein are methods for aligning a molecular wire, by ligating the molecular wire to a double stranded DNA molecule.
    • 本文公开的方法,装置和系统涉及碳纳米管的有序阵列。 在本发明的具体实施方案中,纳米管阵列通过包括将催化剂纳米颗粒140,230连接到聚合物120,210分子,将聚合物120,210分子连接到基底上的方法形成,除去聚合物120,210分子并产生碳 催化剂纳米颗粒140,230上的纳米管。聚合物120,210分子可以使用自组装或分子对准技术以有序图案附着到基底上。 纳米管阵列可以附着到基板的选定区域110,310。 在所选择的区域110,310内,纳米管是非随机分布的。 本文公开的其它实施方案涉及包括连接到衬底的纳米管的有序阵列和包括通过所要求保护的方法产生的连接到衬底的碳纳米管的有序阵列的系统的装置。 在某些实施方案中,本文提供了通过将分子线连接到双链DNA分子来对齐分子线的方法。
    • 6. 发明授权
    • Methods and device for biomolecule characterization
    • 生物分子表征的方法和装置
    • US07744816B2
    • 2010-06-29
    • US10138157
    • 2002-05-01
    • Xing SuAndrew A. Berlin
    • Xing SuAndrew A. Berlin
    • G01N33/48
    • G01N33/48721C12Q2563/179C12Q2565/631G01N33/6803
    • The methods and apparatus 100, disclosed herein are of use for sequencing 150 and/or identifying 160 proteins 230, 310, polypeptides 230, 310 or peptides 230, 310. Proteins 230, 310 containing labeled amino acid residues may be synthesized and passed through nanopores 255, 330. A detector 257, 345 operably coupled to a nanopore 255, 330 may detect labeled amino acid residues as they pass through the nanopore 255, 330. Distance maps 140 for each type of labeled amino acid residue may be compiled. The distance maps 140 may be used to sequence 150 and/or identify 160 the protein 230, 310. In different embodiments of the invention, amino acid residues labeled with luminescent labels 235, 245 or nanoparticles 315 may be detected using photodetectors 257 or electrical detectors 345. Apparatus 100 of use for protein 230, 310 sequencing 150 and/or identification 160 are also disclosed herein.
    • 本文公开的方法和装置100可用于测序150和/或鉴定160个蛋白质230,310,多肽230,310或肽230,310。可以合成含有标记的氨基酸残基的蛋白质230,310并通过纳米孔 可操作地耦合到纳米孔255,330的检测器257,345可以在标记的氨基酸残基通过纳米孔255,330时检测标记的氨基酸残基。可以编译每种类型的标记的氨基酸残基的距离图140。 距离图140可以用于序列150和/或识别160蛋白230,310。在本发明的不同实施方案中,用发光标记235,245或纳米颗粒315标记的氨基酸残基可以使用光电检测器257或电检测器 本文还公开了用于蛋白质230,3001测序150和/或鉴定物160的装置100。
    • 10. 发明授权
    • Methods and device for analyte characterization
    • 用于分析物表征的方法和装置
    • US08278055B2
    • 2012-10-02
    • US10697682
    • 2003-10-29
    • Xing SuAndrew A. Berlin
    • Xing SuAndrew A. Berlin
    • G01N33/53C12Q1/68
    • G01N33/48721G01N33/582G01N33/6803G01N33/6818
    • The methods and apparatus, disclosed herein are of use for sequencing and/or identifying proteins, polypeptides and/or peptides. Proteins containing labeled amino acid residues may be synthesized and passed through nanopores. A detector operably coupled to a nanopore may detect labeled amino acid residues as they pass through the nanopore. Distance maps for each type of labeled amino acid residue may be compiled. The distance maps may be used to sequence and/or identify the protein. Apparatus of use for protein sequencing and/or identification is also disclosed herein. In alternative methods, other types of analytes may be analyzed by the same techniques.
    • 本文公开的方法和装置可用于测序和/或鉴定蛋白质,多肽和/或肽。 含有标记氨基酸残基的蛋白质可以合成并通过纳米孔。 可操作地耦合到纳米孔的检测器可以在通过纳米孔时检测标记的氨基酸残基。 可以编制每种类型的标记氨基酸残基的距离图。 距离图可以用于序列和/或鉴定蛋白质。 本文还公开了用于蛋白质测序和/或鉴定的装置。 在替代方法中,可以通过相同的技术分析其它类型的分析物。