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    • 3. 发明申请
    • METHODS OF PRODUCING CARBON NANOTUBES USING PEPTIDE OR NUCLEIC ACID MICROPATTERNING
    • 使用肽或核酸微生物生产碳纳米管的方法
    • WO2005066367A2
    • 2005-07-21
    • PCT/US2004/043364
    • 2004-12-24
    • INTEL CORPORATIONSU, XingSUNDARARAJAN, NarayanYAMAKAWA, MineoBERLIN, AndrewSUN, LeiZHANG, Yuegang
    • SU, XingSUNDARARAJAN, NarayanYAMAKAWA, MineoBERLIN, AndrewSUN, LeiZHANG, Yuegang
    • C12Q1/68
    • 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 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,通过包括将催化剂纳米颗粒(140,230)附着到聚合物(120,210)分子上的方法形成纳米管阵列,将聚合物(120,210)分子连接到基底上,去除聚合物 120,210)分子并在催化剂纳米颗粒(140,230)上产生碳纳米管。 聚合物(120,210)分子对齐技术。 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的装置以及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。 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。
    • 4. 发明申请
    • METHODS AND COMPOSITIONS FOR DETECTING NUCLEIC ACIDS USING SCANNING PROBE MICROSCOPY AND NANOCODES
    • 使用扫描探针显微镜和纳米级检测核酸的方法和组合物
    • WO2005066368A2
    • 2005-07-21
    • PCT/US2004/043632
    • 2004-12-28
    • INTEL CORPORATIONBERLIN, AndrewYAMAKAWA, Mineo
    • BERLIN, AndrewYAMAKAWA, Mineo
    • C12Q1/68
    • C12Q1/6874B82Y5/00B82Y10/00C12Q2565/601C12Q2563/155C12Q2525/179
    • A method for determining a nucleotide sequence of a nucleic acid is provided that includes contacting the nucleic acid with a series of labeled oligonucleotides for binding to the nucleic acid, wherein each labeled oligonucleotide includes a known nucleotide sequence and a molecular nanocode. The nanocode of an isolated labeled oligonucleotides that binds to the nucleic acid is then detected using SPM. Nanocodes of the present invention in certain aspects include detectable features beyond the arrangement of tags that encode information about the barcoded object, which assist in detecting the tags that encode information about the barcoded object. The detectable features include structures of a nanocode or associated with a nanocode, referred to herein as detectable feature tags, for error checking/error-correction, encryption, and data reduction/compression.
    • 提供了用于确定核酸的核苷酸序列的方法,其包括使核酸与一系列用于结合核酸的标记的寡核苷酸接触,其中每个标记的寡核苷酸包括已知的核苷酸序列和分子纳代码。 然后使用SPM检测与核酸结合的分离的标记寡核苷酸的纳代码。 在某些方面,本发明的纳代码包括超过编码关于条形码对象的信息的标签布置的可检测特征,其有助于检测编码关于条形码对象的信息的标签。 可检测特征包括用于错误校验/纠错,加密和数据缩减/压缩的纳代码或与纳代码相关联的结构,这里称为可检测特征标签。
    • 10. 发明申请
    • METHODS TO INCREASE NUCLEOTIDE SIGNALS BY RAMAN SCATTERING
    • 通过拉曼散射增加核苷酸信号的方法
    • WO2003078649A2
    • 2003-09-25
    • PCT/US2003/007641
    • 2003-03-11
    • INTEL CORPORATION
    • SU, XingBERLIN, AndrewKOO, Tae-WoongCHAN, SelenaSUNDARARAJAN, NarayanYAMAKAWA, Mineo
    • C12Q
    • C12Q1/6869C12Q1/6816C12Q1/6825C12Q1/6872C12Q2565/632C12Q2563/155C12Q2521/319
    • The methods and apparatus disclosed herein concern nucleic acid sequencing by enhanced Raman spectroscopy. In certain embodiments of the invention, nucleotides are covalently attached to Raman labels before incorporation into a nucleic acid (13). Exonuclease (15) treatment of the labeled nucleic acid (13) results in the release of labeled nucleotides (16, 130), which are detected by Raman spectroscopy. In alternative embodiments of the invention, nucleotides (16, 130) released from a nucleic acid (13) by exonuclease (15) treatment are covalently cross-linked to silver or gold nanoparticles (140) and detected by surface enhanced Raman spectroscopy (SERS), surface enhanced resonance Raman spectroscopy (SERRS) and/or coherent anti-Stokes Raman spectroscopy (CARS). Other embodiments of the invention concern apparatus (10, 100, 210) for nucleic acid sequencing.
    • 本文公开的方法和装置涉及通过增强拉曼光谱进行的核酸测序。 在本发明的某些实施方案中,核苷酸在掺入核酸(13)之前共价连接到拉曼标记上。 标记核酸(13)的外切核酸酶(15)处理导致标记的核苷酸(16,130)的释放,其通过拉曼光谱法检测。 在本发明的替代实施方案中,通过核酸外切酶(15)处理从核酸(13)释放的核苷酸(16,130)与银或金纳米颗粒(140)共价交联并通过表面增强拉曼光谱(SERS)检测, ,表面增强共振拉曼光谱(SERRS)和/或相干反斯托克斯拉曼光谱(CARS)。 本发明的其它实施方案涉及用于核酸测序的装置(10,100,210)。