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    • 61. 发明申请
    • Methods for Exchanging Data Amongst Mobile Applications Using Superlinks
    • 使用超级链接交换移动应用数据的方法
    • US20150215383A1
    • 2015-07-30
    • US14532754
    • 2014-11-04
    • Lei SunLi HongHan Cheng Liang
    • Lei SunLi HongHan Cheng Liang
    • H04L29/08G06F17/30
    • H04W4/00G06F17/30876G06F17/3089H04L67/02H04L67/10H04L67/22
    • In one embodiment, a server receives a first URL link from a first mobile device of a first user. In response to the first URL link, the server determines whether a first mobile application that is associated with the URL link has been installed at the first mobile device. If the first mobile application has not been installed at the first mobile device, interactive data of the first user with respect to the first URL link is collected and stored in an event database of the server. If the first mobile application has been installed at the first mobile device, first data that is associated with the first URL link is retrieved from the link database and a second URL link is generated, the second URL link including the first data embedded therein. The second URL link is transmitted to the first mobile device.
    • 在一个实施例中,服务器从第一用户的第一移动设备接收第一URL链接。 响应于第一URL链接,服务器确定与URL链接相关联的第一移动应用是否已经安装在第一移动设备。 如果第一移动应用程序尚未安装在第一移动设备处,则第一用户相对于第一URL链接的交互式数据被收集并存储在服务器的事件数据库中。 如果第一移动应用已经安装在第一移动设备上,则从链接数据库中检索与第一URL链接相关联的第一数据,并且生成第二URL链接,第二URL链接包括嵌入其中的第一数据。 第二URL链接被发送到第一移动设备。
    • 65. 发明申请
    • Programmable molecular barcodes
    • 可编程分子条形码
    • US20060199216A1
    • 2006-09-07
    • US11430590
    • 2006-05-08
    • Xing SuTae-Woong KooAndrew BerlinLei SunNarayanan SundararajanMineo Yamakawa
    • Xing SuTae-Woong KooAndrew BerlinLei SunNarayanan SundararajanMineo Yamakawa
    • C12Q1/68G01N33/551
    • B82Y10/00B82Y5/00C12Q1/6816G06K19/06028C12Q2525/161C12Q2537/143C12Q2565/1025
    • The present disclosure concerns methods for producing and/or using molecular barcodes. In certain embodiments of the invention, the barcodes comprise polymer backbones that may contain one or more branch structures. Tags may be attached to the backbone and/or branch structures. The barcode may also comprise a probe that can bind to a target, such as proteins, nucleic acids and other biomolecules or aggregates. Different barcodes may be distinguished by the type and location of the tags. In other embodiments, barcodes may be produced by hybridization of one or more tagged oligonucleotides to a template, comprising a container section and a probe section. The tagged oligonucleotides may be designed as modular code sections, to form different barcodes specific for different targets. In alternative embodiments, barcodes may be prepared by polymerization of monomeric units. Bound barcodes may be detected by various imaging modalities, such as, surface plasmon resonance, fluorescent or Raman spectroscopy.
    • 本公开涉及用于生产和/或使用分子条形码的方法。 在本发明的某些实施方案中,条形码包含可包含一个或多个分支结构的聚合物主链。 标签可以附加到骨干和/或分支结构。 条形码还可以包含可以与靶标结合的探针,例如蛋白质,核酸和其他生物分子或聚集体。 可以通过标签的类型和位置区分不同的条形码。 在其它实施方案中,条形码可以通过将一个或多个标记的寡核苷酸与包含容器部分和探针部分的模板杂交来产生。 标记的寡核苷酸可以被设计为模块代码部分,以形成针对不同靶标的不同条形码。 在替代实施例中,条形码可以通过单体单元的聚合来制备。 绑定的条形码可以通过各种成像模式来检测,例如表面等离子体共振,荧光或拉曼光谱。
    • 67. 发明申请
    • Biomolecular analysis by rolling circle amplification and sers detection
    • 通过滚动圆放大和检测器进行生物分子分析
    • US20060099636A1
    • 2006-05-11
    • US11313108
    • 2005-12-19
    • Lei SunXing Su
    • Lei SunXing Su
    • C12Q1/68C12P19/34C12M1/34
    • C12Q1/6804C12Q1/6816C12Q1/682G01N21/658C12Q2565/632C12Q2565/518C12Q2531/125C12Q2563/179
    • The present methods, compositions and systems are concerned with biomolecule 130 detection, identification and/or quantification by rolling circle amplification (RCA) and Raman detection. In particular embodiments of the invention, the RCA is exponential RCA or linear RCA. In some embodiments of the invention, the Raman detection is SERS or SERRS. The circular DNA template 150, 210, 310 to be amplified may comprise one or more polythymidine 320 residues, resulting in amplification products 170, 230, 250, 330, 410 containing multiple polyadenylate 340, 420 residues. The polyadenylates 340, 420 may be directly detected by Raman detection. Alternatively, one or more Raman labels may be incorporated into the amplification products 170, 230, 250, 330, 410 to facilitate Raman detection. Because of the amplification produced by LRCA or ERCA and the enhanced Raman signal produced by multiple polyadenylates 340, 420 and/or Raman labels, detection of single copy biomolecules 130 is feasible using the disclosed methods, compositions and/or systems.
    • 本方法,组合物和系统涉及通过滚环扩增(RCA)和拉曼检测的生物分子130检测,鉴定和/或定量。 在本发明的特定实施例中,RCA是指数RCA或线性RCA。 在本发明的一些实施方案中,拉曼检测是SERS或SERRS。 要扩增的环状DNA模板150,210,310可以包含一个或多个多胸苷320残基,导致扩增产物170,230,250,330,410含有多个聚腺苷酸340,420个残基。 多聚腺苷酸酯340,420可以通过拉曼检测直接检测。 或者,可以将一个或多个拉曼标记掺入扩增产物170,230,250,330,410以促进拉曼检测。 由于由LRCA或ERCA产生的扩增和由多个多腺苷酸340,420和/或拉曼标记产生的增强的拉曼信号,使用所公开的方法,组合物和/或系统检测单拷贝生物分子130是可行的。