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公开(公告)号:US11268135B2
公开(公告)日:2022-03-08
申请号:US16300469
申请日:2017-05-10
发明人: Nicolas Arab
IPC分类号: C12Q1/6818 , G01N33/542 , C12Q1/68
摘要: Embodiments of this invention are directed towards the sensitive, fast, and accurate identification and/or characterization of a single cell or bacterium, particularly phenotypic characterization. Certain aspects of the invention include assays that include functional nucleic acid probes (FNAPs). FNAPs can be used to generate deoxyribozyme cleavage cascades (DRCC) initiated by activation of a FNAP resulting in a detectable signal from a single cell.
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公开(公告)号:US11061018B2
公开(公告)日:2021-07-13
申请号:US16656962
申请日:2019-10-18
发明人: Nicolas Arab , Ross Johnson
摘要: Certain embodiments of the invention are directed to evaluating and identifying cells by recording and interpreting a time-dependent signal produced by unique cell respiration and permeability attributes of isolated viable cells.
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3.
公开(公告)号:US20210331178A1
公开(公告)日:2021-10-28
申请号:US17195206
申请日:2021-03-08
发明人: Ross Johnson , Jonathan Isom , David Bussian , Nicolas Arab
摘要: An apparatus for loading and imaging a microfluidic chip can comprise a housing having walls that define a vacuum chamber and a first receptacle disposed within the vacuum chamber, the first receptacle defining a space for receiving one or more microfluidic chips. The apparatus can also include a negative pressure source, a light source, and an optical sensor coupled to the housing. The negative pressure source can be configured to reduce pressure within the vacuum chamber, the light source can be positioned to illuminate at least a portion of the space for receiving the chip(s), and the optical sensor can be positioned to capture an image of at least a portion of the space for receiving the chip(s).
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4.
公开(公告)号:US10953404B1
公开(公告)日:2021-03-23
申请号:US16858282
申请日:2020-04-24
发明人: Ross Johnson , Jonathan Isom , David Bussian , Nicolas Arab
摘要: An apparatus for loading and imaging a microfluidic chip can comprise a housing having walls that define a vacuum chamber and a first receptacle disposed within the vacuum chamber, the first receptacle defining a space for receiving one or more microfluidic chips. The apparatus can also include a negative pressure source, a light source, and an optical sensor coupled to the housing. The negative pressure source can be configured to reduce pressure within the vacuum chamber, the light source can be positioned to illuminate at least a portion of the space for receiving the chip(s), and the optical sensor can be positioned to capture an image of at least a portion of the space for receiving the chip(s).
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5.
公开(公告)号:US12128415B2
公开(公告)日:2024-10-29
申请号:US17195206
申请日:2021-03-08
发明人: Ross Johnson , Jonathan Isom , David Bussian , Nicolas Arab
CPC分类号: B01L9/527 , B01L1/02 , B01L3/502715 , B01L3/50273 , B01L3/502784 , G01N21/31 , B01L2200/0642 , B01L2200/0647 , B01L2300/0663 , B01L2400/049
摘要: An apparatus for loading and imaging a microfluidic chip can comprise a housing having walls that define a vacuum chamber and a first receptacle disposed within the vacuum chamber, the first receptacle defining a space for receiving one or more microfluidic chips. The apparatus can also include a negative pressure source, a light source, and an optical sensor coupled to the housing. The negative pressure source can be configured to reduce pressure within the vacuum chamber, the light source can be positioned to illuminate at least a portion of the space for receiving the chip(s), and the optical sensor can be positioned to capture an image of at least a portion of the space for receiving the chip(s).
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公开(公告)号:US11344890B2
公开(公告)日:2022-05-31
申请号:US16661829
申请日:2019-10-23
发明人: Nicolas Arab , Ross Johnson , David Bussian , Jon Isom
摘要: A microfluidic chip that can have a body defining a microfluidic network including a test volume, one or more ports, and one or more channels in fluid communication between the port(s) and the test volume. Gas can be removed from the test volume before a sample liquid is introduced therein by reducing pressure at a first one of the port(s), optionally while the liquid is disposed in the port. Liquid in the first port can be introduced into the test volume by increasing pressure at the first port. The microfluidic network can define one or more droplet-generating regions in which at least one of the channel(s) defines a constriction and/or two or more of the channels connect at a junction. Liquid flowing from the first port can pass through at least one of the droplet-generating region(s) and to the test volume.
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公开(公告)号:US20210053065A1
公开(公告)日:2021-02-25
申请号:US16998646
申请日:2020-08-20
发明人: Nicolas Arab , Ross Johnson
摘要: A method of analyzing a sample comprising one or more species of microorganisms can include generating first droplets such that each of one or more microorganisms of a first portion of the sample is encapsulated within one of the first droplets and, for each of one or more aliquots of a second portion of the sample, second droplets such that each of one or more microorganisms of the aliquot is encapsulated within one of the second droplets. First and second sets of data can be captured, the first set indicative of the identity and quantity of encapsulated microorganism(s) of the first portion of the sample and the second set indicative of a phenotypic response of encapsulated microorganism(s) of the aliquot(s) to one or more test reagents. A target species' phenotypic response to the test reagent(s) is determinable at least by referencing the second data set to the first data set.
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公开(公告)号:US11959910B2
公开(公告)日:2024-04-16
申请号:US17372957
申请日:2021-07-12
发明人: Nicolas Arab , Ross Johnson
IPC分类号: C12Q1/04 , C12Q1/18 , G01N15/14 , G01N21/64 , G01N33/50 , G01N33/58 , G01N15/10 , G01N15/1404
CPC分类号: G01N33/5091 , C12Q1/04 , C12Q1/18 , G01N15/1463 , G01N21/6428 , G01N33/5011 , G01N33/582 , G01N2015/1006 , G01N2015/1406 , G01N2015/1481 , G01N2201/0621 , G01N2800/26
摘要: Certain embodiments of the invention are directed to evaluating and identifying cells by recording and interpreting a time-dependent signal produced by unique cell respiration and permeability attributes of isolated viable cells.
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