Wireless Extender Secure Discovery and Provisioning
    61.
    发明申请
    Wireless Extender Secure Discovery and Provisioning 有权
    无线扩展器安全发现和配置

    公开(公告)号:US20120230491A1

    公开(公告)日:2012-09-13

    申请号:US13478003

    申请日:2012-05-22

    IPC分类号: H04W48/16 H04L9/00

    摘要: According to embodiments of the invention, a first wireless access point discovers a second wireless access point, the first wireless access point tunes its radio and privacy settings, without user input, based upon parameters automatically exchanged in response to the discovery of the second wireless access point, and a secure direct wireless connection is established between the first and second wireless access points using the radio and privacy settings. Adding the first wireless to an existing mesh network includes a determination of the best available direct wireless connection.

    摘要翻译: 根据本发明的实施例,第一无线接入点发现第二无线接入点,第一无线接入点基于根据第二无线接入的发现自动交换的参数而调整其无线电和隐私设置,无需用户输入 并且使用无线电和隐私设置在第一和第二无线接入点之间建立安全的直接无线连接。 将第一个无线网络添加到现有的网状网络中包括确定最佳可用的直接无线连接。

    Method for the quantitative evaluation of sex hormones in a serum sample
    62.
    发明授权
    Method for the quantitative evaluation of sex hormones in a serum sample 失效
    血清样品中性激素定量评估方法

    公开(公告)号:US08114682B2

    公开(公告)日:2012-02-14

    申请号:US12442379

    申请日:2007-09-17

    IPC分类号: G01N33/553

    摘要: This invention discloses using SPR technology to simultaneously and quantitatively measure the concentrations of different sex hormones in a serum sample, which can be used to evaluate different clinical situations. It also discloses an efficient formula to make a mixed SAM that can greatly enhance the immobilization ability of the metal surface in SPR based techniques, which is good for the immobilization of relevant antibodies used for the detection of representative sex hormones in a serum sample.

    摘要翻译: 本发明公开了使用SPR技术同时并定量测定血清样品中不同性激素的浓度,可用于评估不同临床情况。 它还公开了一种制备混合SAM的有效配方,可以大大增强金属表面在基于SPR的技术中的固定能力,这有利于固定用于检测血清样品中代表性性激素的相关抗体。

    Method for quantitative detection of diabetes related immunological markers
    63.
    发明授权
    Method for quantitative detection of diabetes related immunological markers 失效
    糖尿病相关免疫学标志物定量检测方法

    公开(公告)号:US08110408B2

    公开(公告)日:2012-02-07

    申请号:US12441530

    申请日:2007-09-17

    IPC分类号: G01N33/553

    摘要: This invention discloses using SPR technology to simultaneously and quantitatively measure the concentrations of diabetes related immunological makers in a serum sample, which can be used to diagnose and/or early diagnose diabetes as well as to predict the onset risk of diabetes in first-degree relatives. It also discloses an efficient formula to make a mixed SAM that can greatly enhance the immobilization ability of the metal surface in SPR based techniques, which is good for the immobilization of relevant antigens and antibodies used for the detection of respective diabetes related immunological makers in a serum sample.

    摘要翻译: 本发明公开了使用SPR技术同时并定量测定血清样品中糖尿病相关免疫学家的浓度,可用于诊断和/或早期诊断糖尿病,并预测一级亲属糖尿病的发病风险 。 它还公开了一种制备混合SAM的有效配方,可以大大增强金属表面在基于SPR的技术中的固定能力,这有利于固定相关抗原和抗体,用于检测相应的糖尿病相关免疫学家 血清样品。

    WIRELESS EXTENDER SECURE DISCOVERY AND PROVISIONING
    64.
    发明申请
    WIRELESS EXTENDER SECURE DISCOVERY AND PROVISIONING 有权
    无线扩展安全发现和提供

    公开(公告)号:US20110158127A1

    公开(公告)日:2011-06-30

    申请号:US12724363

    申请日:2010-03-15

    IPC分类号: H04W48/16

    摘要: According to embodiments of the invention, a first wireless access point discovers a second wireless access point, the first wireless access point tunes its radio and privacy settings, without user input, based upon parameters automatically exchanged in response to the discovery of the second wireless access point, and a secure direct wireless connection is established between the first and second wireless access points using the radio and privacy settings. Adding the first wireless to an existing mesh network includes a determination of the best available direct wireless connection.

    摘要翻译: 根据本发明的实施例,第一无线接入点发现第二无线接入点,第一无线接入点基于根据第二无线接入的发现自动交换的参数而调整其无线电和隐私设置,无需用户输入 并且使用无线电和隐私设置在第一和第二无线接入点之间建立安全的直接无线连接。 将第一个无线网络添加到现有的网状网络中包括确定最佳可用的直接无线连接。

    LOW SURFACE ENERGY ADHESIVE
    65.
    发明申请
    LOW SURFACE ENERGY ADHESIVE 审中-公开
    低表面能量粘合剂

    公开(公告)号:US20110104486A1

    公开(公告)日:2011-05-05

    申请号:US13002358

    申请日:2009-06-10

    摘要: Adhesives suitable for use with low surface energy materials are described. The adhesive contain an acrylic copolymer, a high glass transition temperature tackifier and a low glass transition temperature tackifier. The acrylic copolymer is the reaction product of a first alkyl(meth)acrylate having at least 5 carbon atoms in the alkyl group, a second alkyl(meth)acrylate having 1 to 4 carbon atoms in the alkyl group, and a vinyl carboxylic acid. Both tackifiers have a Tg greater than the Tg of the acrylic copolymer. The high glass transition temperature tackifier has a Tg of at least 20° C. and the low glass transition temperature tackifier has a Tg of less than 0° C.

    摘要翻译: 描述适用于低表面能材料的粘合剂。 粘合剂含有丙烯酸共聚物,高玻璃化转变温度增粘剂和低玻璃化转变温度增粘剂。 丙烯酸共聚物是烷基中具有至少5个碳原子的(甲基)丙烯酸烷基酯的第一烷基酯,烷基中的具有1至4个碳原子的第(甲基)丙烯酸烷基酯和乙烯基羧酸的反应产物。 两种增粘剂的Tg都大于丙烯酸共聚物的Tg。 高玻璃化转变温度增粘剂的Tg至少为20℃,低玻璃化转变温度增粘剂的Tg小于0℃。

    METHOD OF SURFACE PLASMON RESONANCE (SPR) TO DETECT GENOMIC DISORDERS FOR POSTNATAL DIAGNOSIS
    67.
    发明申请
    METHOD OF SURFACE PLASMON RESONANCE (SPR) TO DETECT GENOMIC DISORDERS FOR POSTNATAL DIAGNOSIS 审中-公开
    表面等离子体共振(SPR)检测基因疾病的方法用于后期诊断

    公开(公告)号:US20100047789A1

    公开(公告)日:2010-02-25

    申请号:US12441527

    申请日:2007-08-20

    申请人: Zhong Chen Ning Liu

    发明人: Zhong Chen Ning Liu

    IPC分类号: C12Q1/68 C12M1/34

    摘要: The present invention discloses using SPR technology to postnatally detect specific DNA loss or gain related to some genomic disorders. An efficient formula to make a mixed SAM that can greatly enhance the immobilization ability of the metal surface in SPR based techniques, which is good for the immobilization of DNA markers used for the identification of subtelomere imbalances and chromosome microdeletion syndromes is also disclosed.

    摘要翻译: 本发明公开了使用SPR技术来检测与某些基因组紊乱有关的特异性DNA损失或增益。 还公开了一种制备混合SAM的有效配方,可以大大增强金属表面在基于SPR的技术中的固定能力,这对于用于鉴定亚种不平衡和染色体微缺失综合征的DNA标记的固定是有利的。

    METHOD TO REMOVE REPETITIVE SEQUENCES FROM HUMAN DNA
    68.
    发明申请
    METHOD TO REMOVE REPETITIVE SEQUENCES FROM HUMAN DNA 审中-公开
    从人类DNA中移除重复序列的方法

    公开(公告)号:US20100021971A1

    公开(公告)日:2010-01-28

    申请号:US12441525

    申请日:2007-08-16

    申请人: Zhong Chen Ning Liu

    发明人: Zhong Chen Ning Liu

    IPC分类号: C12P19/34

    摘要: The invention discloses an innovative method to deplete repetitive sequences from human DNA. The method comprises (a) providing a source DNA containing both unique and repetitive sequences and sonicating the source DNA to smaller fragments; (b) providing a driver DNA containing sequences complementary to the repetitive sequences of the source DNA and labeled with a non-radioactive label, (c) hybridizing the source DNA and the driver DNA in the presence of a molecule that binds the label to form a complex; (d) removing the hybridized repetitive sequences from the complex by using RNAase and electrophoresis or by incubating with a mixture of phenol, chloroform, and ethanol; and (e) recovering the remaining source DNA wherein said repetitive sequences being significantly removed.

    摘要翻译: 本发明公开了一种从人类DNA中消耗重复序列的创新方法。 该方法包括(a)提供含有唯一和重复序列的源DNA,并将源DNA超声处理成较小的片段; (b)提供含有与源DNA的重复序列互补并且用非放射性标记标记的序列的驱动DNA,(c)在结合标记的分子存在下使源DNA与驱动DNA杂交形成 一个复杂的 (d)通过使用RNA酶和电泳或通过与苯酚,氯仿和乙醇的混合物一起孵育从复合物中除去杂交的重复序列; 和(e)回收剩余的源DNA,其中显着除去所述重复序列。

    METHOD OF DETECTING GENOMIC ABERRATIONS FOR PRENATAL DIAGNOSIS
    70.
    发明申请
    METHOD OF DETECTING GENOMIC ABERRATIONS FOR PRENATAL DIAGNOSIS 审中-公开
    检测基因治疗对于临床诊断的方法

    公开(公告)号:US20100015619A1

    公开(公告)日:2010-01-21

    申请号:US12445516

    申请日:2007-09-21

    IPC分类号: C12Q1/68

    CPC分类号: C12Q1/6883 C12Q2600/16

    摘要: This invention relates to assays used to detect and confirm genomic aberrations, such as chromosomes 13, 18, 21, X and Y aneuploidy as well as 22q11.2 deletions, for prenatal diagnosis. For the detection, combined STR markers (all tetra-nucleotide repeats) are employed to cover different chromosome regions. For the confirmation step, individual chromosome specific STR markers (tetra-nucleotide repeats) are utilized. This invention particularly relates to multiplex analysis for the presence or absence of STR markers in genomic DNA isolated from peripheral blood, amniotic fluid, cultured amniocytes, chorionic villi, or fetal cells existing in maternal blood. This invention offers an efficient approach to identify chromosomal abnormalities by using STR markers.

    摘要翻译: 本发明涉及用于检测和确认基因组畸变的测定法,例如染色体13,18,21,X和Y非整倍性以及22q11.2缺失,用于产前诊断。 为了检测,使用组合的STR标记(全部四核苷酸重复)来覆盖不同的染色体区域。 对于确认步骤,使用个体染色体特异性STR标记(四核苷酸重复)。 本发明特别涉及从外周血,羊水,培养的羊膜细胞,绒毛膜绒毛或存在于母体血液中的胎儿细胞分离的基因组DNA中存在或不存在STR标记的多重分析。 本发明提供了通过使用STR标记鉴定染色体异常的有效方法。