SYSTEM AND METHOD FOR ELECTRIC MACHINE COOLING

    公开(公告)号:US20230369945A1

    公开(公告)日:2023-11-16

    申请号:US17743707

    申请日:2022-05-13

    IPC分类号: H02K9/19 H02K1/16 H02K3/12

    CPC分类号: H02K9/19 H02K1/16 H02K3/12

    摘要: Stator packages and electric machines, and methods for cooling same, are disclosed herein. In an example embodiment, an electric machine includes a rotor, and a stator package having one or more stator coils, stator core portions, and a heat exchanger. The stator core portions and heat exchanger are arranged successively along a central axis, with the heat exchanger being positioned between the stator core portions. Each of the stator coils is arranged to extend along/within the stator core portions and heat exchanger. The heat exchanger includes walls forming passageways configured so that coolant entering the heat exchanger via an inlet both flows circumferentially from the inlet to an outlet, and additionally flows in an undulating manner both radially inwardly and outwardly substantially in between outer and inner wall surfaces of the heat exchanger, such that the coolant cools the one or more stator coils and the stator core portions.

    OPTICAL FINGERPRINTING OF NUCLEIC ACID SEQUENCES
    9.
    发明申请
    OPTICAL FINGERPRINTING OF NUCLEIC ACID SEQUENCES 审中-公开
    核酸序列的光学指纹

    公开(公告)号:US20070148674A1

    公开(公告)日:2007-06-28

    申请号:US11615695

    申请日:2006-12-22

    IPC分类号: C12Q1/68 C12M3/00

    摘要: The present invention provides methods and apparatus for the optical fingerprinting of nucleic acid molecules. In certain embodiments, the invention provides methods for labeling nucleic acid molecules using-site-specific nucleic acid binding partners that bind to nucleic acids without cleaving the molecule. The nucleic acid binding partners can be labeled directly with a fluorophore, such as a quantum dot (QD), or indirectly. Examples of suitable binding partners include cut-deficient restriction endonucleases (cdREs), transcription factors, the binding domains of nucleic acid polymerases, antibodies and the like. The methods disclosed make the assembly of fingerprint contigs easier and allows for digitizing the results so as to provide for easier computer manipulation and assembly. The invention also includes a microarray, the microarray designed to provide for easy deposition and high-throughput fingerprinting. The invention also provides for methods of using the microarrays. The invention also provides kits for the use of the invention.

    摘要翻译: 本发明提供了核酸分子的光学指纹图谱的方法和装置。 在某些实施方案中,本发明提供了使用与核酸结合但不裂解该分子的位点特异性核酸结合配偶体标记核酸分子的方法。 核酸结合配偶体可直接用荧光团(例如量子点(QD))或间接地标记。 合适的结合配偶体的实例包括切断缺陷型限制性内切核酸酶(cdRE),转录因子,核酸聚合酶的结合结构域,抗体等。 所公开的方法使得指纹重叠群的组装更容易,并允许数字化结果,从而提供更容易的计算机操纵和组装。 本发明还包括微阵列,微阵列被设计成提供易于沉积和高通量指纹。 本发明还提供了使用微阵列的方法。 本发明还提供了用于本发明的试剂盒。

    Method for producing L-beta-lysine
    10.
    发明申请
    Method for producing L-beta-lysine 有权
    生产L-β-赖氨酸的方法

    公开(公告)号:US20020173637A1

    公开(公告)日:2002-11-21

    申请号:US09847010

    申请日:2001-05-01

    IPC分类号: C07H021/04

    CPC分类号: C12N9/90 H01L22/20

    摘要: Purified null-amino acids are of considerable interest in the preparation of pharmacologically active compounds. Although enantiomerically pure null-amino acids, such as L-null-lysine, can be produced by standard chemical synthesis, this traditional approach is time consuming, requires expensive starting materials, and results in a racemic mixture which must be purified further. However, DNA molecules encoding lysine 2,3-aminomutase can be used to prepare L-null-lysine by methods that avoid the pitfalls of chemical synthesis. In particular, L-null-lysine can be synthesized by cultures of host cells that express recombinant lysine 2,3-aminomutase. Alternatively, such recombinant host cells can provide a source for isolating quantities of lysine 2,3-aminomutase, which in turn, can be used to produce L-null-lysine in vitro.

    摘要翻译: 纯化的β-氨基酸在药理活性化合物的制备中具有相当大的兴趣。 尽管通过标准化学合成可以生产对映异构体纯的β-氨基酸,例如L-β-赖氨酸,但是这种传统方法是耗时的,需要昂贵的起始原料,并且导致必须进一步纯化的外消旋混合物。 然而,编码赖氨酸2,3-氨基变位酶的DNA分子可用于通过避免化学合成缺陷的方法制备L-β-赖氨酸。 特别地,L-β-赖氨酸可以通过表达重组赖氨酸2,3-氨基变位酶的宿主细胞的培养物合成。 或者,这样的重组宿主细胞可提供用于分离赖氨酸2,3-氨基变位酶的来源,其依次可用于在体外产生L-β-赖氨酸。