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    • 1. 发明授权
    • Cellular analysis using Raman surface scanning
    • 使用拉曼表面扫描的细胞分析
    • US07776547B2
    • 2010-08-17
    • US11027470
    • 2004-12-30
    • Mark RothAndrew BerlinSelena ChanTae-Woong KooXing SuLei Sun
    • Mark RothAndrew BerlinSelena ChanTae-Woong KooXing SuLei Sun
    • G01N33/53
    • G01N33/54366G01N33/54373G01N33/58Y10T436/10
    • Methods and apparatus are provided for assaying cell samples, which may be living cells, using probes labeled with composite organic-inorganic nanoparticles (COINs) and microspheres with COINs embedded within a polymer matrix to which the probe moiety is attached. COINs intrinsically produce SERS signals upon laser irradiation, making COIN-labeled probes particularly suitable in a variety of methods for assaying cells, including biological molecules that may be contained on or within cells, most of which are not inherently Raman-active. The invention provides variations of the sandwich immunoassay employing both specific and degenerate binding, methods for reverse phase assay of tissue samples and cell microstructures, in solution displacement and competition assays, and the like. Systems and chips useful for practicing the invention assays are also provided.
    • 提供了用于使用用复合有机 - 无机纳米颗粒(COIN)标记的探针和嵌入探针部分所连接的聚合物基质内的COIN的微球来测定可能为活细胞的细胞样品的方法和装置。 COIN在激光照射下固有地产生SERS信号,使得COIN标记的探针特别适用于多种测定细胞的方法,包括可能包含在细胞内或细胞内的生物分子,其中大部分不是固有的拉曼活性的。 本发明提供使用特异性和简并结合的夹心免疫测定的变体,组织样品和细胞微结构的反相测定方法,溶液置换和竞争测定等。 还提供了用于实施本发明测定的系统和芯片。
    • 4. 发明申请
    • Programmable molecular barcodes
    • 可编程分子条形码
    • US20070054288A1
    • 2007-03-08
    • US11430612
    • 2006-05-08
    • Xing SuTae-Woong KooAndrew BerlinLei SunNarayanan SundararajanMineo Yamakawa
    • Xing SuTae-Woong KooAndrew BerlinLei SunNarayanan SundararajanMineo Yamakawa
    • C12Q1/68C12M1/34G06K7/10
    • B82Y10/00B82Y5/00C12Q1/6816G06K19/06028C12Q2525/161C12Q2537/143C12Q2565/1025
    • The present disclosure concerns methods for producing and/or using molecular barcodes. In certain embodiments of the invention, the barcodes comprise polymer backbones that may contain one or more branch structures. Tags may be attached to the backbone and/or branch structures. The barcode may also comprise a probe that can bind to a target, such as proteins, nucleic acids and other biomolecules or aggregates. Different barcodes may be distinguished by the type and location of the tags. In other embodiments, barcodes may be produced by hybridization of one or more tagged oligonucleotides to a template, comprising a container section and a probe section. The tagged oligonucleotides may be designed as modular code sections, to form different barcodes specific for different targets. In alternative embodiments, barcodes may be prepared by polymerization of monomeric units. Bound barcodes may be detected by various imaging modalities, such as, surface plasmon resonance, fluorescent or Raman spectroscopy.
    • 本公开涉及用于生产和/或使用分子条形码的方法。 在本发明的某些实施方案中,条形码包含可包含一个或多个分支结构的聚合物主链。 标签可以附加到骨干和/或分支结构。 条形码还可以包含可以与靶标结合的探针,例如蛋白质,核酸和其他生物分子或聚集体。 可以通过标签的类型和位置区分不同的条形码。 在其它实施方案中,条形码可以通过将一个或多个标记的寡核苷酸与包含容器部分和探针部分的模板杂交来产生。 标记的寡核苷酸可以被设计为模块代码部分,以形成针对不同靶标的不同条形码。 在替代实施例中,条形码可以通过单体单元的聚合来制备。 可以通过各种成像方式,例如表面等离子体共振,荧光或拉曼光谱来检测结合条形码。
    • 8. 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
    • US20050151126A1
    • 2005-07-14
    • US10750141
    • 2003-12-31
    • Mineo YamakawaYeugang ZhangXing SuLei SunAndrew BerlinNarayanan Sundararajan
    • Mineo YamakawaYeugang ZhangXing SuLei SunAndrew BerlinNarayanan Sundararajan
    • C01B31/02D01F9/127H01L51/00H01L51/30D01F9/12H01L29/06
    • 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。