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    • 4. 发明申请
    • PROCESS FOR SELF-ASSEMBLY OF STRUCTURES IN A LIQUID
    • 液体中自组织的方法
    • US20080032330A1
    • 2008-02-07
    • US11835054
    • 2007-08-07
    • Gafur ZainievInlik ZainievTimur Zainiev
    • Gafur ZainievInlik ZainievTimur Zainiev
    • C12P21/00C12M1/00C12P19/34
    • C12P19/34B01L3/5027C12Q1/6869
    • A process and apparatus for self-assembling a number of elements and determining their sequence is provided. In the field of DNA analysis, an iterative process is disclosed wherein an apparatus with a set of reaction chambers in which a species of recognition element nucleotides are differentially added and subjected to a polymerization reaction allows recognition of which species is next in sequence on a template strand as measured by a detector in a detection area. Fractional concentration stepwise addition of the identified species then determines if an element repeat exists. The position in the sequence is then completed by addition of a saturating amount of building element to complete the polymerization reaction on all structure strands. The process is repeated until the entire structure is complete and the sequence identified.
    • 提供了一种用于自组装多个元件并确定其顺序的过程和装置。 在DNA分析领域中,公开了一种迭代方法,其中具有一组反应室的装置,其中识别元件核苷酸的种类被差异添加并进行聚合反应允许在模板上依次识别下一个物种 在检测区域中由检测器测量。 分数浓度逐步添加所识别的物种然后确定元素重复是否存在。 然后通过加入饱和量的构建元素完成序列中的位置以在所有结构链上完成聚合反应。 重复该过程,直到整个结构完成并确定序列。
    • 6. 发明申请
    • NUCLEIC ACID ARRAY HAVING FIXED NUCLEIC ACID ANTI-PROBES AND COMPLEMENTARY FREE NUCLEIC ACID PROBES
    • 具有固定核酸抗原探针和完全免费的核酸探针的核酸阵列
    • US20080044821A1
    • 2008-02-21
    • US11465870
    • 2006-08-21
    • Gafur ZainievInlik Zainiev
    • Gafur ZainievInlik Zainiev
    • C12Q1/68C07H21/04
    • C12Q1/6837C12Q2537/161
    • A process for identifying a complementary nucleic acid probe to a target nucleic acid involves forming an array of spots where each spot of the array has an immobilized nucleic acid anti-probe to which is hybridized a nucleic acid probe. The array of the anti-probe-probe complex is denatured. The nucleic acid probes are then moved into a target chamber that includes a target nucleic acid. Hybridization conditions are established to form double-stranded complexation between the target nucleic acid and nucleic acid probes in instances where the target nucleic acid has a sequence complementary. The nucleic acid probes noncomplementary to the target nucleic acid are allowed to rehybridize with anti-probes. Determining whether the anti-probe spots exposed to nucleic acid probes noncomplementary to the target nucleic acid are single stranded after exposure to noncomplementary nucleic acid probes provides information as to target nucleic acid sequence.
    • 用于鉴定靶核酸的互补核酸探针的方法包括形成阵列阵列,其中阵列的每个点具有与核酸探针杂交的固定的核酸抗探针。 抗探针 - 探针复合物的阵列变性。 然后将核酸探针移动到包括靶核酸的靶室中。 建立杂交条件以在目标核酸具有序列互补性的情况下在靶核酸和核酸探针之间形成双链复合。 允许与靶核酸不互补的核酸探针用抗探针重新杂化。 确定在暴露于非互补核酸探针之后,暴露于与靶核酸不互补的核酸探针的抗探针点是单链提供关于靶核酸序列的信息。
    • 7. 发明申请
    • MICROSEPARATION STRUCTURE AND DEVICES FORMED THEREWITH
    • 微结构及其形成的器件
    • US20100240119A1
    • 2010-09-23
    • US12708256
    • 2010-02-18
    • Inlik Zainiev
    • Inlik Zainiev
    • B01D11/04C12M1/34B01D15/08
    • B01L3/502753B01D15/34B01L3/5023B01L2300/041B01L2300/0681B01L2300/0825B01L2300/087B01L2400/0406B01L2400/0481B01L2400/0683B01L2400/0694
    • A microseparation structure is provided that includes a top surface defining a first chamber. A second chamber is provided that is in fluid communication with the first chamber and characterized by a volume less than the volume of the first chamber. At least one hole extends in fluid communication with the second chamber to transmit fluids into a capillary draw void volume filled with a capillary draw-inducing agent such that liquid placed in the first chamber is drawn through the second chamber and through the hole to the capillary draw void volume filled with capillary draw-inducing agent. Particles of interest within the liquid are unable to pass into the hole and are therefore isolated within the second chamber. This structure is amenable to forming into a compact chromatographic filtration media made up of multiple such structures that is well suited for sealed testing for diseases such as malaria.
    • 提供了一种微分离结构,其包括限定第一室的顶表面。 提供了与第一室流体连通的第二室,其特征在于体积小于第一室的体积。 至少一个孔与第二室流体连通地延伸,以将流体传输到填充有毛细管牵引诱导剂的毛细管抽取空隙体积中,使得放置在第一腔室中的液体被抽吸通过第二腔室并通过该孔进入毛细管 绘制填充有毛细管牵引诱导剂的空隙体积。 液体内感兴趣的颗粒不能进入孔,因此在第二室内被隔离。 该结构适于形成由多种这样的结构组成的紧密色谱过滤介质,其非常适合于诸如疟疾的疾病的密封测试。
    • 8. 发明申请
    • NUCLEIC ACID ARRAY HAVING FIXED NUCLEIC ACID ANTI-PROBES AND COMPLEMENTARY FREE NUCLEIC ACID PROBES
    • 具有固定核酸抗原探针和完全免费的核酸探针的核酸阵列
    • US20100056388A1
    • 2010-03-04
    • US12571676
    • 2009-10-01
    • Gafur ZainievInlik Zainiev
    • Gafur ZainievInlik Zainiev
    • C40B30/04C40B40/06
    • C12Q1/6837C12Q2537/161
    • A process for identifying a complementary nucleic acid probe to a target nucleic acid involves forming an array of spots where each spot of the array has an immobilized nucleic acid anti-probe to which is hybridized a nucleic acid probe. The array of the anti-probe-probe complex is denatured. The nucleic acid probes are then moved into a target chamber that includes a target nucleic acid. Hybridization conditions are established to form double-stranded complexation between the target nucleic acid and nucleic acid probes in instances where the target nucleic acid has a sequence complementary. The nucleic acid probes noncomplementary to the target nucleic acid are allowed to rehybridize with anti-probes. Determining whether the anti-probe spots exposed to nucleic acid probes noncomplementary to the target nucleic acid are single stranded after exposure to noncomplementary nucleic acid probes provides information as to target nucleic acid sequence.
    • 用于鉴定靶核酸的互补核酸探针的方法包括形成阵列阵列,其中阵列的每个点具有与核酸探针杂交的固定的核酸抗探针。 抗探针 - 探针复合物的阵列变性。 然后将核酸探针移动到包括靶核酸的靶室中。 建立杂交条件以在目标核酸具有序列互补性的情况下在靶核酸和核酸探针之间形成双链复合。 允许与靶核酸不互补的核酸探针用抗探针重新杂化。 确定在暴露于非互补核酸探针之后,暴露于与靶核酸不互补的核酸探针的抗探针点是单链提供关于靶核酸序列的信息。
    • 9. 发明申请
    • CLOSED SPACE DISPOSABLE MICRO-REACTOR AND USES THEREOF
    • 封闭空间可置换微反应器及其用途
    • US20090047191A1
    • 2009-02-19
    • US12135597
    • 2008-06-09
    • Gafur ZainievInlik Zainiev
    • Gafur ZainievInlik Zainiev
    • B01J19/00
    • B01L3/50273B01L3/502715B01L2300/0627B01L2300/0838B01L2400/0487
    • A closed space disposable micro-reactor is provided with a capillary vessel with a first end and a second end, a first closed air chamber wherein said first end of the capillary vessel opens into the first closed air chamber; and a second closed air chamber wherein the second end of the capillary chamber opens into said second closed air chamber. The capillary vessel is pre-filled with a liquid sample. A droplet of reagent set in proximity to the first end of the capillary vessel is provided. Also provided is a partner capillary vessel with a first partner end and a second partner end, and a third closed air chamber wherein the first partner end of the partner capillary vessel opens into the second closed air chamber, and the second partner end opens to the second air chamber.
    • 封闭空间一次性微反应器设置有具有第一端和第二端的毛细管容器,第一封闭空气室,其中所述毛细管的所述第一端通入第一封闭空气室; 以及第二封闭空气室,其中毛细管室的第二端通向所述第二封闭空气室。 毛细血管预先填充有液体样品。 设置在毛细血管的第一端附近设置的一滴试剂。 还提供了具有第一伴侣端和第二伙伴端的伴侣毛细管,以及第三封闭空气室,其中配对毛细血管的第一配对端打开到第二封闭空气室中,并且第二配对端打开至 第二个空气室。