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公开(公告)号:US10940473B2
公开(公告)日:2021-03-09
申请号:US16396137
申请日:2019-04-26
Applicant: California Institute of Technology
Inventor: Jong Wook Hong , Vincent Studer , W. French Anderson , Stephen R. Quake , Jared Leadbetter
IPC: C12Q1/68 , B01L3/00 , C12Q1/6806
Abstract: Nucleic acid from cells and viruses sampled from a variety of environments may purified and expressed utilizing microfluidic techniques. Individual or small groups of cells or viruses may be isolated in microfluidic chambers by dilution, sorting, and/or segmentation. The isolated cells or viruses may be lysed directly in the microfluidic chamber, and the resulting nucleic acid purified by exposure to affinity beads. Subsequent elution of the purified nucleic acid may be followed by ligation and cell transformation, all within the same microfluidic chip. Cell isolation, lysis, and nucleic acid purification may be performed utilizing a highly parallelized microfluidic architecture to construct gDNA and cDNA libraries.
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公开(公告)号:US20140065653A1
公开(公告)日:2014-03-06
申请号:US13679328
申请日:2012-11-16
Applicant: California Institute of Technology
Inventor: Sebastian J. Maerkl , Todd A. Thorsen , Xiaoyan Bao , Stephen R. Quake , Vincent Studer
IPC: C12Q1/28
CPC classification number: C12Q1/28 , B01L3/5025 , B01L3/50273 , B01L3/502738 , B01L2300/0861 , B01L2300/0887 , B01L2400/0481 , B01L2400/0655 , B81B2201/0214 , B81B2201/054 , B81B2201/07 , B81C1/00119 , F15C5/00 , F16K11/20 , F16K99/0001 , F16K99/0015 , F16K99/0059 , F16K2099/0074 , F16K2099/0076 , F16K2099/0078 , F16K2099/008 , F16K2099/0084 , F16K2099/0094 , Y10T137/0318 , Y10T137/0329 , Y10T137/2224 , Y10T137/85938 , Y10T137/87249
Abstract: High-density microfluidic chips contain plumbing networks with thousands of micromechanical valves and hundreds of individually addressable chambers. These fluidic devices are analogous to electronic integrated circuits fabricated using large scale integration (LSI). A component of these networks is the fluidic multiplexor, which is a combinatorial array of binary valve patterns that exponentially increases the processing power of a network by allowing complex fluid manipulations with a minimal number of inputs. These integrated microfluidic networks can be used to construct a variety of highly complex microfluidic devices, for example the microfluidic analog of a comparator array, and a microfluidic memory storage device resembling electronic random access memories.
Abstract translation: 高密度微流控芯片包含具有数千个微机械阀门和数百个单独可寻址腔室的管道网络。 这些流体装置类似于使用大规模集成(LSI)制造的电子集成电路。 这些网络的一个组件是流体多路复用器,它是二进制阀模式的组合阵列,通过允许使用最少数量的输入的复杂流体操纵来指数地增加网络的处理能力。 这些集成的微流体网络可用于构建各种高度复杂的微流体装置,例如比较器阵列的微流体模拟装置和类似于电子随机存取存储器的微流体存储器存储装置。
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公开(公告)号:US20200147608A1
公开(公告)日:2020-05-14
申请号:US16396137
申请日:2019-04-26
Applicant: California Institute of Technology
Inventor: Jong Wook Hong , Vincent Studer , W. French Anderson , Stephen R. Quake , Jared Leadbetter
IPC: B01L3/00 , C12Q1/6806
Abstract: Nucleic acid from cells and viruses sampled from a variety of environments may purified and expressed utilizing microfluidic techniques. Individual or small groups of cells or viruses may be isolated in microfluidic chambers by dilution, sorting, and/or segmentation. The isolated cells or viruses may be lysed directly in the microfluidic chamber, and the resulting nucleic acid purified by exposure to affinity beads. Subsequent elution of the purified nucleic acid may be followed by ligation and cell transformation, all within the same microfluidic chip. Cell isolation, lysis, and nucleic acid purification may be performed utilizing a highly parallelized microfluidic architecture to construct gDNA and cDNA libraries.
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公开(公告)号:US09579650B2
公开(公告)日:2017-02-28
申请号:US14494284
申请日:2014-09-23
Applicant: California Institute of Technology
Inventor: Jong Wook Hong , Vincent Studer , W. French Anderson , Stephen R. Quake , Jared Leadbetter
CPC classification number: B01L3/502715 , B01L3/50273 , B01L3/502738 , B01L3/502761 , B01L2200/10 , B01L2300/0809 , B01L2300/0816 , B01L2300/0877 , B01L2300/1827 , B01L2400/0481 , B01L2400/0655 , C12Q1/6806 , C12Q2565/629
Abstract: Nucleic acid from cells and viruses sampled from a variety of environments may purified and expressed utilizing microfluidic techniques. In accordance with one embodiment of the present invention, individual or small groups of cells or viruses may be isolated in microfluidic chambers by dilution, sorting, and/or segmentation. The isolated cells or viruses may be lysed directly in the microfluidic chamber, and the resulting nucleic acid purified by exposure to affinity beads. Subsequent elution of the purified nucleic acid may be followed by ligation and cell transformation, all within the same microfluidic chip. In one specific application, cell isolation, lysis, and nucleic acid purification may be performed utilizing a highly parallelized microfluidic architecture to construct gDNA and cDNA libraries.
Abstract translation: 来自从各种环境取样的细胞和病毒的核酸可以利用微流体技术纯化和表达。 根据本发明的一个实施方案,可通过稀释,分选和/或分割在微流体室中分离单个或小组的细胞或病毒。 分离的细胞或病毒可以直接在微流体室中裂解,并且通过暴露于亲和珠来纯化得到的核酸。 随后洗脱纯化的核酸之后可以连接和细胞转化,全部在相同的微流体芯片内。 在一个具体应用中,细胞分离,裂解和核酸纯化可以使用高度并行的微流体结构来构建gDNA和cDNA文库。
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公开(公告)号:US20150238960A1
公开(公告)日:2015-08-27
申请号:US14494284
申请日:2014-09-23
Applicant: California Institute of Technology
Inventor: Jong Wook Hong , Vincent Studer , W. French Anderson , Stephen R. Quake , Jared Leadbetter
CPC classification number: B01L3/502715 , B01L3/50273 , B01L3/502738 , B01L3/502761 , B01L2200/10 , B01L2300/0809 , B01L2300/0816 , B01L2300/0877 , B01L2300/1827 , B01L2400/0481 , B01L2400/0655 , C12Q1/6806 , C12Q2565/629
Abstract: Nucleic acid from cells and viruses sampled from a variety of environments may purified and expressed utilizing microfluidic techniques. In accordance with one embodiment of the present invention, individual or small groups of cells or viruses may be isolated in microfluidic chambers by dilution, sorting, and/or segmentation. The isolated cells or viruses may be lysed directly in the microfluidic chamber, and the resulting nucleic acid purified by exposure to affinity beads. Subsequent elution of the purified nucleic acid may be followed by ligation and cell transformation, all within the same microfluidic chip. In one specific application, cell isolation, lysis, and nucleic acid purification may be performed utilizing a highly parallelized microfluidic architecture to construct gDNA and cDNA libraries.
Abstract translation: 来自从各种环境取样的细胞和病毒的核酸可以利用微流体技术纯化和表达。 根据本发明的一个实施方案,可通过稀释,分选和/或分割在微流体室中分离单个或小组的细胞或病毒。 分离的细胞或病毒可以直接在微流体室中裂解,并且通过暴露于亲和珠来纯化得到的核酸。 随后洗脱纯化的核酸之后可以连接和细胞转化,全部在相同的微流体芯片内。 在一个具体应用中,细胞分离,裂解和核酸纯化可以使用高度并行的微流体结构来构建gDNA和cDNA文库。
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公开(公告)号:US10328428B2
公开(公告)日:2019-06-25
申请号:US15406451
申请日:2017-01-13
Applicant: California Institute of Technology
Inventor: Jong Wook Hong , Vincent Studer , W. French Anderson , Stephen R. Quake , Jared Leadbetter
IPC: C12Q1/68 , B01L3/00 , C12Q1/6806
Abstract: Nucleic acid from cells and viruses sampled from a variety of environments may purified and expressed utilizing microfluidic techniques. In accordance with one embodiment of the present invention, individual or small groups of cells or viruses may be isolated in microfluidic chambers by dilution, sorting, and/or segmentation. The isolated cells or viruses may be lysed directly in the microfluidic chamber, and the resulting nucleic acid purified by exposure to affinity beads. Subsequent elution of the purified nucleic acid may be followed by ligation and cell transformation, all within the same microfluidic chip. In one specific application, cell isolation, lysis, and nucleic acid purification may be performed utilizing a highly parallelized microfluidic architecture to construct gDNA and cDNA libraries.
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公开(公告)号:US20190009272A1
公开(公告)日:2019-01-10
申请号:US15406451
申请日:2017-01-13
Applicant: California Institute of Technology
Inventor: Jong Wook Hong , Vincent Studer , W. French Anderson , Stephen R. Quake , Jared Leadbetter
IPC: B01L3/00 , C12Q1/6806
CPC classification number: B01L3/502715 , B01L3/50273 , B01L3/502738 , B01L3/502761 , B01L2200/10 , B01L2300/0809 , B01L2300/0816 , B01L2300/0877 , B01L2300/1827 , B01L2400/0481 , B01L2400/0655 , C12Q1/6806 , C12Q2565/629
Abstract: Nucleic acid from cells and viruses sampled from a variety of environments may purified and expressed utilizing microfluidic techniques. In accordance with one embodiment of the present invention, individual or small groups of cells or viruses may be isolated in microfluidic chambers by dilution, sorting, and/or segmentation. The isolated cells or viruses may be lysed directly in the microfluidic chamber, and the resulting nucleic acid purified by exposure to affinity beads. Subsequent elution of the purified nucleic acid may be followed by ligation and cell transformation, all within the same microfluidic chip. In one specific application, cell isolation, lysis, and nucleic acid purification may be performed utilizing a highly parallelized microfluidic architecture to construct gDNA and cDNA libraries.
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公开(公告)号:US09714443B2
公开(公告)日:2017-07-25
申请号:US13679328
申请日:2012-11-16
Applicant: California Institute of Technology
Inventor: Sebastian J. Maerkl , Todd A. Thorsen , Xiaoyan Bao , Stephen R. Quake , Vincent Studer
CPC classification number: C12Q1/28 , B01L3/5025 , B01L3/50273 , B01L3/502738 , B01L2300/0861 , B01L2300/0887 , B01L2400/0481 , B01L2400/0655 , B81B2201/0214 , B81B2201/054 , B81B2201/07 , B81C1/00119 , F15C5/00 , F16K11/20 , F16K99/0001 , F16K99/0015 , F16K99/0059 , F16K2099/0074 , F16K2099/0076 , F16K2099/0078 , F16K2099/008 , F16K2099/0084 , F16K2099/0094 , Y10T137/0318 , Y10T137/0329 , Y10T137/2224 , Y10T137/85938 , Y10T137/87249
Abstract: High-density microfluidic chips contain plumbing networks with thousands of micromechanical valves and hundreds of individually addressable chambers. These fluidic devices are analogous to electronic integrated circuits fabricated using large scale integration (LSI). A component of these networks is the fluidic multiplexor, which is a combinatorial array of binary valve patterns that exponentially increases the processing power of a network by allowing complex fluid manipulations with a minimal number of inputs. These integrated microfluidic networks can be used to construct a variety of highly complex microfluidic devices, for example the microfluidic analog of a comparator array, and a microfluidic memory storage device resembling electronic random access memories.
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