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    • 1. 发明授权
    • Assays and other reactions involving droplets
    • 测定和其他涉及液滴的反应
    • US09029085B2
    • 2015-05-12
    • US12529926
    • 2008-03-07
    • Jeremy AgrestiLiang-Yin ChuDavid A. WeitzJin-Woong KimAmy RowatMorten SommerGautam DantasGeorge Church
    • Jeremy AgrestiLiang-Yin ChuDavid A. WeitzJin-Woong KimAmy RowatMorten SommerGautam DantasGeorge Church
    • C12Q1/68C12P19/34B01J13/00B01F3/08B01F13/00
    • C12P19/34B01F3/0807B01F3/0811B01F13/0062B01F13/0071B01F2215/0037B01J13/0052B01J13/0065B01L3/502784C12Q1/6834C12Q1/6848C12Q1/686G01N15/1404G01N2015/1006
    • The present invention generally relates to droplets and/or emulsions, such as multiple emulsions. In some cases, the droplets and/or emulsions may be used in assays, and in certain embodiments, the droplet or emulsion may be hardened to form a gel. In some aspects, a heterogeneous assay can be performed using a gel. For example, a droplet may be hardened to form a gel, where the droplet contains a cell, DNA, or other suitable species. The gel may be exposed to a reactant, and the reactant may interact with the gel and/or with the cell, DNA, etc., in some fashion. For example, the reactant may diffuse through the gel, or the hardened particle may liquefy to form a liquid state, allowing the reactant to interact with the cell. As a specific example, DNA contained within a gel particle may be subjected to PCR (polymerase chain reaction) amplification, e.g., by using PCR primers able to bind to the gel as it forms. As the DNA is amplified using PCR, some of the DNA will be bound to the gel via the PCR primer. After the PCR reaction, unbound DNA may be removed from the gel, e.g., via diffusion or washing. Thus, a gel particle having bound DNA may be formed in one embodiment of the invention.
    • 本发明通常涉及液滴和/或乳液,例如多重乳液。 在一些情况下,液滴和/或乳液可用于测定中,并且在某些实施方案中,液滴或乳液可被硬化以形成凝胶。 在一些方面,可以使用凝胶进行异质测定。 例如,液滴可以被硬化以形成凝胶,其中液滴包含细胞,DNA或其它合适的物质。 凝胶可以暴露于反应物,并且反应物可以以某种方式与凝胶和/或与细胞,DNA等相互作用。 例如,反应物可以扩散通过凝胶,或者硬化的颗粒可以液化以形成液体状态,允许反应物与细胞相互作用。 作为具体实例,包含在凝胶颗粒内的DNA可以进行PCR(聚合酶链式反应)扩增,例如通过使用能够在形成凝胶时结合凝胶的PCR引物。 当使用PCR扩增DNA时,一些DNA将通过PCR引物与凝胶结合。 PCR反应后,未结合的DNA可以从凝胶中去除,例如通过扩散或洗涤。 因此,可以在本发明的一个实施方案中形成具有结合DNA的凝胶颗粒。
    • 2. 发明申请
    • SYSTEMS AND METHODS FOR SPLITTING DROPLETS
    • 用于分割滴液的系统和方法
    • US20140026968A1
    • 2014-01-30
    • US13979984
    • 2012-02-06
    • Adam R. AbateDavid A. Weitz
    • Adam R. AbateDavid A. Weitz
    • B01L3/00
    • B01L3/5027B01L3/502784B01L2200/0673B01L2200/12B01L2300/0816B01L2300/0864B01L2300/123Y10T137/0318Y10T137/85938
    • The present invention generally relates to fluidics and microfluidics and, in particular, to creating droplets in a fluidic system. In some aspects, the present invention is generally directed to systems and methods for splitting a parent droplet into two or more droplets, e.g., by urging the parent droplet towards an obstacle to split the parent droplet. In some cases, the parent droplet is split into at least first and second droplets which each are directed to separate channels. In some cases, the channels may be constructed and arranged such that the droplet velocities of the first and second droplets are substantially the same as the velocity of the parent droplet. In some cases, such droplets may be repeatedly split, e.g., a parent droplet is divided into 2 daughter droplets, then each droplet split again, etc., for example, such that one parent droplet may eventually be split into 22, 23, 24, 25, 26, etc. daughter droplets. In some cases, the daughter droplets may be substantially monodisperse.
    • 本发明一般涉及流体和微流体,特别是涉及在流体系统中产生液滴。 在一些方面,本发明一般涉及用于将母液滴分解为两个或更多个液滴的系统和方法,例如通过将母液滴向障碍物推动以分离母液滴。 在一些情况下,母液滴被分成至少第一和第二液滴,每个液滴被引导到分离的通道。 在一些情况下,可以构造和布置通道,使得第一和第二液滴的液滴速度基本上与母液滴的速度相同。 在一些情况下,这样的液滴可以被重复地分开,例如,母液滴被分成2个子液滴,然后每个液滴再次分离等,例如使得一个亲液滴最终可以分成22,23,24 ,25,26等子液滴。 在一些情况下,子液滴可以是基本上单分散的。
    • 4. 发明申请
    • CONTROL OF EMULSIONS, INCLUDING MULTIPLE EMULSIONS
    • 乳液控制,包括多种乳液
    • US20130046030A1
    • 2013-02-21
    • US13477636
    • 2012-05-22
    • Assaf RotemDavid A. WeitzAdam R. AbateChristian Holtze
    • Assaf RotemDavid A. WeitzAdam R. AbateChristian Holtze
    • B01J13/00B01F5/00
    • B01F3/0811B01F3/0807B01F13/0062B01F13/0084Y10T137/87571
    • The present invention generally relates to emulsions, and more particularly, to double and other multiple emulsions. Certain aspects of the present invention are generally directed to the creation of double emulsions and other multiple emulsions at a common junction of microfluidic channels. In some cases, the microfluidic channels at the common junction may have substantially the same hydrophobicity. In one set of embodiments, a device may include a common junction of six or more channels, where a first fluid flows through one channel, a second fluid flows through two channels, and a third or carrying fluid flows through two more channels, such that a double emulsion of a first droplet of the first fluid, contained in a second droplet of the second fluid, contained by the carrying fluid, flows away from the common junction through a sixth channel.
    • 本发明一般涉及乳液,更具体地说涉及双重和其它多重乳液。 本发明的某些方面通常涉及在微流体通道的共同连接处产生双重乳液和其它多重乳液。 在一些情况下,共同连接处的微流体通道可具有基本上相同的疏水性。 在一组实施例中,装置可以包括六个或更多个通道的公共接头,其中第一流体流过一个通道,第二流体流过两个通道,并且第三或承载流体流过两个以上通道,使得 包含在第二流体的第二液滴中的第一流体的第一液滴的双重乳液由携带流体包含,通过第六通道从公共接头流出。
    • 6. 发明申请
    • SYSTEMS AND METHODS FOR NUCLEIC ACID SEQUENCING
    • 核酸序列的系统和方法
    • US20110267457A1
    • 2011-11-03
    • US12809120
    • 2008-12-19
    • David A WeitzJeremy AgrestiMichael P. WeinerAdam R. AbateTony Hung
    • David A WeitzJeremy AgrestiMichael P. WeinerAdam R. AbateTony Hung
    • C40B30/04C07H1/00H04N7/18G01N33/53
    • C12Q1/6874C12Q2537/143C12Q2563/149
    • The present invention relates to systems and methods for sequencing nucleic acids, including sequencing nucleic acids in fluidic droplets. In one set of embodiments, the method employs sequencing by hybridization using droplets such as microfluidic droplets. In some embodiments, droplets are formed which include a target nucleic acid, a nucleic acid probe, and at least one identification element, such as a fluorescent particle. The nucleic acid probes that hybridize to the target nucleic acid are determined, in some instances, by determining the at least one identification element. The nucleic acid probes that hybridize to the target nucleic acid may be used to determine the sequence of the target nucleic acid. In certain instances, the microfluidic droplets are provided with reagents that modify the nucleic acid probe. In some cases, a droplet, such as those described above, is deformed such that the components of the droplets individually pass a target area.
    • 本发明涉及用于测序核酸的系统和方法,包括以流体液滴测序核酸。 在一组实施方案中,该方法采用使用微滴(例如微流控液滴)的杂交进行测序。 在一些实施方案中,形成液滴,其包括靶核酸,核酸探针和至少一种识别元件,例如荧光颗粒。 在某些情况下,通过确定至少一个识别元件来确定与靶核酸杂交的核酸探针。 与靶核酸杂交的核酸探针可用于测定靶核酸的序列。 在某些情况下,向微流体液滴提供修饰核酸探针的试剂。 在一些情况下,诸如上述那些的液滴变形,使得液滴的组分分别通过目标区域。
    • 9. 发明申请
    • ASSAYS AND OTHER REACTIONS INVOLVING DROPLETS
    • 测量和其他涉及倾销的反应
    • US20100136544A1
    • 2010-06-03
    • US12529926
    • 2008-03-07
    • Jeremy AgrestiLiang-Yin ChuDavid A. WeitzJin-Woong KimAmy RowatMorten SommerGautam DantasGeorge Church
    • Jeremy AgrestiLiang-Yin ChuDavid A. WeitzJin-Woong KimAmy RowatMorten SommerGautam DantasGeorge Church
    • C12Q1/68C12Q1/04
    • C12P19/34B01F3/0807B01F3/0811B01F13/0062B01F13/0071B01F2215/0037B01J13/0052B01J13/0065B01L3/502784C12Q1/6834C12Q1/6848C12Q1/686G01N15/1404G01N2015/1006
    • The present invention generally relates to droplets and/or emulsions, such as multiple emulsions. In some cases, the droplets and/or emulsions may be used in assays, and in certain embodiments, the droplet or emulsion may be hardened to form a gel. In some aspects, a heterogeneous assay can be performed using a gel. For example, a droplet may be hardened to form a gel, where the droplet contains a cell, DNA, or other suitable species. The gel may be exposed to a reactant, and the reactant may interact with the gel and/or with the cell, DNA, etc., in some fashion. For example, the reactant may diffuse through the gel, or the hardened particle may liquefy to form a liquid state, allowing the reactant to interact with the cell. As a specific example, DNA contained within a gel particle may be subjected to PCR (polymerase chain reaction) amplification, e.g., by using PCR primers able to bind to the gel as it forms. As the DNA is amplified using PCR, some of the DNA will be bound to the gel via the PCR primer. After the PCR reaction, unbound DNA may be removed from the gel, e.g., via diffusion or washing. Thus, a gel particle having bound DNA may be formed in one embodiment of the invention.
    • 本发明通常涉及液滴和/或乳液,例如多重乳液。 在一些情况下,液滴和/或乳液可用于测定中,并且在某些实施方案中,液滴或乳液可被硬化以形成凝胶。 在一些方面,可以使用凝胶进行异质测定。 例如,液滴可以被硬化以形成凝胶,其中液滴包含细胞,DNA或其它合适的物质。 凝胶可以暴露于反应物,并且反应物可以以某种方式与凝胶和/或与细胞,DNA等相互作用。 例如,反应物可以扩散通过凝胶,或者硬化的颗粒可以液化以形成液体状态,允许反应物与细胞相互作用。 作为具体实例,包含在凝胶颗粒内的DNA可以进行PCR(聚合酶链式反应)扩增,例如通过使用能够在形成凝胶时结合凝胶的PCR引物。 当使用PCR扩增DNA时,一些DNA将通过PCR引物与凝胶结合。 PCR反应后,未结合的DNA可以从凝胶中去除,例如通过扩散或洗涤。 因此,可以在本发明的一个实施方案中形成具有结合DNA的凝胶颗粒。
    • 10. 发明申请
    • MICROFLUIDIC DROPLETS FOR METABOLIC ENGINEERING AND OTHER APPLICATIONS
    • 用于代谢工程和其他应用的微流控溅射
    • US20100124759A1
    • 2010-05-20
    • US12492830
    • 2009-06-26
    • Benjamin L. WangKatherine J. HumphryDavid A. WeitzGregory Stephanopoulos
    • Benjamin L. WangKatherine J. HumphryDavid A. WeitzGregory Stephanopoulos
    • C12Q1/28C12N1/18C12Q1/26C12N1/20
    • B01L3/502715B01L3/502753B01L3/502761B01L2200/0647B01L2200/0652B01L2200/10B01L2300/0681B01L2300/0816B01L2300/087B01L2400/0421
    • The present invention relates generally to the use of droplets to culture and/or assay cells or other species. In some cases, the cells or other species may be sorted based upon the results of the culture and/or assay. In some embodiments, cells other species can be encapsulated in droplets and exposed to one or more agents (e.g., a sugar, an indicator dye, etc.). For instance, in some cases, exposure of cells to the agents may result in the production of metabolites or other compounds (e.g., amino acids, proteins, organic acids, etc.) which may be, for example, assayed or otherwise determined. In some embodiments, the reaction of an agent with cells and/or other species within a droplet may reveal a property of the cells or other species (e.g., sugar consumption, growth rate, ability to withstand exposure to the agent, etc.). As an example, cells that produce desired metabolites or exhibit certain properties may be separated from the other cells via sorting techniques. Other aspects of the invention relate to devices or kits for implementing such sorts, methods of promoting such techniques, or the like.
    • 本发明一般涉及使用液滴来培养和/或测定细胞或其它物种。 在一些情况下,可以基于培养和/或测定的结果对细胞或其它物种进行分类。 在一些实施方案中,细胞其他物质可以被包封在液滴中并暴露于一种或多种试剂(例如,糖,指示剂染料等)。 例如,在一些情况下,细胞暴露于试剂可导致生成代谢物或其它化合物(例如,氨基酸,蛋白质,有机酸等),其可以例如被测定或以其他方式测定。 在一些实施方案中,药剂与细胞和/或液滴内的其它物质的反应可以揭示细胞或其他物种的性质(例如,糖消耗,生长速率,耐受试剂暴露的能力等)。 作为实例,产生所需代谢物或显示某些特性的细胞可以通过分选技术与其他细胞分离。 本发明的其他方面涉及用于实现这种类型的装置或套件,促进这种技术的方法等。