会员体验
专利管家(专利管理)
工作空间(专利管理)
风险监控(情报监控)
数据分析(专利分析)
侵权分析(诉讼无效)
联系我们
交流群
官方交流:
QQ群: 891211   
微信请扫码    >>>
现在联系顾问~
热词
    • 3. 发明授权
    • Detecting the position of an RFID attached asset
    • 检测RFID附属资产的位置
    • US07378968B2
    • 2008-05-27
    • US11210925
    • 2005-08-24
    • Hao B J WangRong Yao FuSong SongXing Xin GaoZhe XiangJian Huang
    • Hao B J WangRong Yao FuSong SongXing Xin GaoZhe XiangJian Huang
    • G08B13/14
    • G01S5/0018G01S5/02
    • Provides asset position detecting apparatus and methods for determining the correspondence relation between an asset attached to an RFID tag and the position in which the asset is located in a predetermined space range. An example apparatus includes: a movable RFID reader movable in the space range, for detecting whether the asset exists in its read range, and reading the RFID tag attached to the asset within its read range, to obtain the specific identification of the detected asset; and position determining means for determining the position where the reader is located, wherein, when said RFID reader detects that said asset exists in its read range during its movement, the obtained identification of the asset and the current position of the RFID reader are associatively stored in a database, so as to obtain the information regarding the position of said asset.
    • 提供资产位置检测装置和方法,用于确定附着于RFID标签的资产与资产所位于预定空间范围内的位置之间的对应关系。 一种示例性装置包括:在空间范围内可移动的可移动RFID读取器,用于检测资产是否存在于其读取范围内,以及读取在其读取范围内附着于资产的RFID标签,以获得所检测资产的特定标识; 以及位置确定装置,用于确定读取器所在的位置,其中当所述RFID读取器在其移动期间检测到所述资产存在于其读取范围内时,所获得的资产的识别和RFID读取器的当前位置被相关联 在数据库中,以获得关于所述资产的位置的信息。
    • 4. 发明申请
    • Oligonucleotides labeled with a plurality of fluorophores
    • 用多个荧光团标记的寡核苷酸
    • US20050272053A1
    • 2005-12-08
    • US10993625
    • 2004-11-19
    • Fei MaoXing Xin
    • Fei MaoXing Xin
    • C07H20060101C07H21/04C12Q1/68
    • C12Q1/6818C12Q1/6851Y10S435/975C12Q2565/1015C12Q2561/101C12Q2565/1025
    • An embodiment of the invention discloses new methods for designing labeled nucleic acid probes and primers by labeling oligonucleotides with a plurality of spectrally identical or similar dyes and optionally with one or more quencher dyes. Oligonucleotides labeled in accordance with some embodiments of the invention exhibit a detectable increase in signal, for example, fluorescent signal when the labeling dyes are separated from one another. Methods for separating the dye include cleaving the labeled oligonucleotides include using enzymes that have 5′-exonuclease activity. In one embodiment nucleic acid primers of the present invention may fluoresce upon hybridization to a target sequence and incorporation into the amplification product. Nucleic acid probes and primers of the present invention have wide applications ranging from general detection of a target nucleic acid sequence to clinical diagnostics. Major advantages of the oligonucleotides including nucleic acid probes and primers of many embodiments of the present invention are their synthetic simplicity, spectral versatility and superior fluorescent signal.
    • 本发明的一个实施方案公开了通过用多个光谱相同或相似的染料和任选地与一种或多种猝灭剂染料标记寡核苷酸来设计标记的核酸探针和引物的新方法。 根据本发明的一些实施方案标记的寡核苷酸在标记染料彼此分离时表现出可检测的信号增加,例如荧光信号。 用于分离染料的方法包括切割标记的寡核苷酸包括使用具有5'-外切核酸酶活性的酶。 在一个实施方案中,本发明的核酸引物可以在与靶序列杂交时发荧光,并掺入扩增产物。 本发明的核酸探针和引物具有广泛的应用范围,从靶核酸序列的一般检测到临床诊断。 包括本发明许多实施方案的核酸探针和引物的寡核苷酸的主要优点是它们的合成简便性,光谱通用性和优异的荧光信号。
    • 5. 发明授权
    • Oligonucleotides as temperature-sensitive inhibitors for DNA polymerases
    • 寡核苷酸作为DNA聚合酶的温度敏感抑制剂
    • US08530194B2
    • 2013-09-10
    • US12088213
    • 2006-09-26
    • Fei MaoXing Xin
    • Fei MaoXing Xin
    • C12P19/34G01N33/53
    • C12Q1/6848C12Q2527/101C12Q2525/205
    • Aspects of the invention relate to the use of novel oligonucleotides as temperature-sensitive inhibitors for thermostable DNA polymerases. Some inhibitors exhibit temperature-dependent and, in some cases, reversible inhibitory property by changing the conformation of at least a portion of the oligonucleotides from double-stranded to single stranded or in some cases vice versa in a temperature-dependent manner. Aspects also relate to the use of an the inhibitors in a hot-start PCR compositions, wherein the inhibitor may act to suppress the activity of the thermostable DNA polymerase below a desired activation temperature, Tact, and wherein the inhibitor is thermally inactivated above Tact, thus liberating the polymerase activity and initiating the DNA amplification process. Aspects further relate to a procedure for formulating the composition of a hot-start PCR reaction mixture. The hot-start PCR methods disclosed herein are generally faster, more flexible and lower in cost than existing methods.
    • 本发明的方面涉及新型寡核苷酸作为热稳定性DNA聚合酶的温度敏感性抑制剂的用途。 一些抑制剂在温度依赖性方面通过将寡核苷酸的至少一部分构型从双链改变为单链或在一些情况下反之亦然地表现出温度依赖性,并且在一些情况下是可逆抑制性质。 方面还涉及在热启动PCR组合物中使用抑制剂,其中抑制剂可以起作用以将热稳定性DNA聚合酶的活性抑制在所需活化温度Tact以下,并且其中抑制剂在Tact之上热灭活, 从而释放聚合酶活性并引发DNA扩增过程。 方面还涉及用于配制热启动PCR反应混合物的组合物的方法。 本文公开的热启动PCR方法通常比现有方法更快,更灵活并且成本更低。
    • 7. 发明授权
    • Oligonucleotides labeled with a plurality of fluorophores
    • 用多个荧光团标记的寡核苷酸
    • US07667024B2
    • 2010-02-23
    • US10993625
    • 2004-11-19
    • Fei MaoXing Xin
    • Fei MaoXing Xin
    • C07H21/02C07H21/04C12Q1/68C12P19/34
    • C12Q1/6818C12Q1/6851Y10S435/975C12Q2565/1015C12Q2561/101C12Q2565/1025
    • An embodiment of the invention discloses new methods for designing labeled nucleic acid probes and primers by labeling oligonucleotides with a plurality of spectrally identical or similar dyes and optionally with one or more quencher dyes. Oligonucleotides labeled in accordance with some embodiments of the invention exhibit a detectable increase in signal, for example, fluorescent signal when the labeling dyes are separated from one another. Methods for separating the dye include cleaving the labeled oligonucleotides include using enzymes that have 5′-exonuclease activity. In one embodiment nucleic acid primers of the present invention may fluoresce upon hybridization to a target sequence and incorporation into the amplification product. Nucleic acid probes and primers of the present invention have wide applications ranging from general detection of a target nucleic acid sequence to clinical diagnostics. Major advantages of the oligonucleotides including nucleic acid probes and primers of many embodiments of the present invention are their synthetic simplicity, spectral versatility and superior fluorescent signal.
    • 本发明的一个实施方案公开了通过用多个光谱相同或相似的染料和任选地与一种或多种猝灭剂染料标记寡核苷酸来设计标记的核酸探针和引物的新方法。 根据本发明的一些实施方案标记的寡核苷酸在标记染料彼此分离时表现出可检测的信号增加,例如荧光信号。 用于分离染料的方法包括切割标记的寡核苷酸包括使用具有5'-外切核酸酶活性的酶。 在一个实施方案中,本发明的核酸引物可以在与靶序列杂交时发荧光,并掺入扩增产物。 本发明的核酸探针和引物具有广泛的应用范围,从靶核酸序列的一般检测到临床诊断。 包括本发明许多实施方案的核酸探针和引物的寡核苷酸的主要优点是它们的合成简便性,光谱通用性和优异的荧光信号。
    • 8. 发明申请
    • OLIGONUCLEOTIDES AS TEMPERATURE-SENSITIVE INHIBITORS FOR DNA POLYMERASES
    • 寡核苷酸作为DNA聚合酶的温敏敏感抑制剂
    • US20090047714A1
    • 2009-02-19
    • US12088213
    • 2006-09-26
    • Fei MaoXing Xin
    • Fei MaoXing Xin
    • C12P19/34C07H21/04C12N9/00
    • C12Q1/6848C12Q2527/101C12Q2525/205
    • Aspects of the invention relate to the use of novel oligonucleotides as temperature-sensitive inhibitors for thermostable DNA polymerases. Some inhibitors exhibit temperature-dependent and, in some cases, reversible inhibitory property by changing the conformation of at least a portion of the oligonucleotides from double-stranded to single stranded or in some cases vice versa in a temperature-dependent manner. Aspects also relate to the use of an the inhibitors in a hot-start PCR compositions, wherein the inhibitor may act to suppress the activity of the thermostable DNA polymerase below a desired activation temperature, Tact, and wherein the inhibitor is thermally inactivated above Tact, thus liberating the polymerase activity and initiating the DNA amplification process. Aspects further relate to a procedure for formulating the composition of a hot-start PCR reaction mixture. The hot-start PCR methods disclosed herein are generally faster, more flexible and lower in cost than existing methods.
    • 本发明的方面涉及新型寡核苷酸作为热稳定性DNA聚合酶的温度敏感性抑制剂的用途。 一些抑制剂在温度依赖性方面通过将寡核苷酸的至少一部分构型从双链改变为单链或在一些情况下反之亦然地表现出温度依赖性,并且在一些情况下是可逆抑制性质。 方面还涉及在热启动PCR组合物中使用抑制剂,其中抑制剂可以起作用以将热稳定性DNA聚合酶的活性抑制在所需活化温度Tact以下,并且其中抑制剂在Tact之上热灭活, 从而释放聚合酶活性并引发DNA扩增过程。 方面还涉及用于配制热启动PCR反应混合物的组合物的方法。 本文公开的热启动PCR方法通常比现有方法更快,更灵活并且成本更低。