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    • 3. 发明申请
    • CONTACT DISPENSING OF CELLS INTO MULTI-WELL DEVICES
    • 将电池分配到多个设备中
    • WO2017205687A1
    • 2017-11-30
    • PCT/US2017/034568
    • 2017-05-25
    • TAKARA BIO USA, INC.
    • HUSAIN, Syed A.GRISWOLD, Bradley L.SRINIVASAN, Maithreyan
    • B01L3/00G01N1/40G01N15/10
    • The present disclosure provides methods, devices, assemblies, and systems for contact dispensing of cells into multi-well devices. For example, provided herein are systems and methods for contact dispensing a dispense volume into a plurality of wells of a multi-well device, where the multi-well device has a hydrophobic top surface (e.g., a contact agent greater than 140 degrees, including greater than 165 degrees) and wells which have a relatively hydrophilic well surface (e.g., contact angle of 65-80 degrees). In some embodiments, a dispensing tip has a hanging drop of liquid (e.g., containing a cell) that is touched off onto the hydrophobic top surface of the multi-well device such that is repelled by the top surface and collected into, and attracted by, the relatively hydrophilic surface of the wells.
    • 本公开提供了用于将细胞接触分配到多孔装置中的方法,装置,组件和系统。 例如,本文提供用于将分配体积接触分配到多孔装置的多个孔中的系统和方法,其中多孔装置具有疏水顶面(例如,大于140度的接触剂,包括 大于165度)和具有相对亲水井表面(例如,65-80度的接触角)的井。 在一些实施例中,分配尖端具有悬挂在多孔装置的疏水顶表面上的液滴(例如,包含细胞)的悬滴,从而被顶表面排斥并被收集到并被吸引 ,这些孔相对亲水的表面。
    • 6. 发明申请
    • METHODS FOR PREPARING A NEXT GENERATION SEQUENCING (NGS) LIBRARY FROM A RIBONUCLEIC ACID (RNA) SAMPLE AND COMPOSITIONS FOR PRACTICING THE SAME
    • 用于制备来自核糖核酸(RNA)样品的下一个产生序列(NGS)图谱的方法和用于实施其的组合物
    • WO2017048993A1
    • 2017-03-23
    • PCT/US2016/051989
    • 2016-09-15
    • TAKARA BIO USA, INC.
    • CHANG, CynthiaBOSTICK, Magnolia
    • G06F19/10G06F19/20G06F19/22C40B40/06C40B40/08
    • C12N15/1093C12N15/1096C12Q2525/191
    • Methods of preparing a next generation sequencing (NGS) library from a ribonucleic acid (RNA) sample are provided. Aspects of the methods include combining the RNA sample with a first strand cDNA primer and a template switch oligonucleotide under first strand cDNA synthesis conditions, where one of the first strand cDNA primer and the template switch oligonucleotide includes a first post-tagmentation amplification primer binding domain. The resultant product is subjected to amplification conditions sufficient to produce a double stranded cDNA, which is then tagmented with a transposome that includes a second post-tagmentation amplification primer binding domain. The tagmented sample is then subjected to amplificationconditions using first and second post-tagmentation amplification primers that include sequencing platform adapter constructs to produce a NGS library. Aspects of the invention further include compositions produced by the methods and kits that find use in practicing the methods.
    • 提供了从核糖核酸(RNA)样品制备下一代测序(NGS)文库的方法。 所述方法的方面包括在第一链cDNA合成条件下将RNA样品与第一链cDNA引物和模板切换寡核苷酸组合,其中第一链cDNA引物和模板切换寡核苷酸之一包含第一后标记扩增引物结合结构域 。 对所得产物进行足以产生双链cDNA的扩增条件,然后用包含第二后标记扩增引物结合结构域的转座子进行标记。 然后使用包括测序平台适配器构建体的第一和第二后标记扩增引物对标记的样品进行扩增条件以产生NGS文库。 本发明的方面还包括通过用于实施该方法的方法和试剂盒产生的组合物。