-
公开(公告)号：US08614266B2
公开(公告)日：2013-12-24
申请号：US13102029
申请日：2011-05-05
申请人： Haiying Li , William Lee Harrison
发明人： Haiying Li , William Lee Harrison
CPC分类号： H01L23/293 , C08G59/226 , C08G59/32 , C08G59/38 , C08G59/50 , C08L63/00 , C08L2666/22 , C09J163/00 , H01L2924/0002 , H01L2924/00
摘要： A potting material for an electronic component, an electronic component, and a process for positioning ferrites in an electronic material are disclosed. The potting material is formed by curing a mixture. The mixture includes an epoxy component, an organic amine hardener, a viscosity-controlling agent, and a silica. The potting material has a coefficient of thermal expansion between an inorganic ferrite coefficient of thermal expansion and an organic substrate coefficient of thermal expansion of the electronic component. The potting material includes a rigidity permitting via drilling by one or more of mechanical drilling and laser burning.
摘要翻译： 公开了一种用于电子部件的灌封材料，电子部件以及将铁氧体定位在电子材料中的工艺。 灌封材料通过固化混合物形成。 该混合物包括环氧组分，有机胺硬化剂，粘度控制剂和二氧化硅。 封装材料具有无机铁氧体热膨胀系数与电子部件的有机基板热膨胀系数之间的热膨胀系数。 灌封材料包括通过一次或多次机械钻孔和激光燃烧钻孔所允许的刚度。
-
公开(公告)号：US09115396B2
公开(公告)日：2015-08-25
申请号：US13177772
申请日：2011-07-07
CPC分类号： C12N15/1065 , C12N15/10 , C12N15/1093 , C12P19/34 , C12Q1/6806 , C12Q1/6855 , C12Q1/6869 , C12Q1/6874 , C12Q2535/122 , C12Q2521/507
摘要： Compositions of transposome complexes for generating DNA fragments with specific 5′- and 3′-tags. Kits for generating libraries for sequencing, with transposome complexes, enzymes, oligonucleotides or other components.
摘要翻译： 用于产生具有特异性5'-和3'标签的DNA片段的转座子复合物的组合物。 用于产生用于测序的文库的试剂盒，具有转座体复合物，酶，寡核苷酸或其它组分。
-
3.发明申请TRANSPOSON END COMPOSITIONS AND METHODS FOR MODIFYING NUCLEIC ACIDS 有权TRANSPOSON END COMPOSITIONS AND METHODS FOR MODIZING NUCLEIC ACIDS公开(公告)号：US20130196860A1
公开(公告)日：2013-08-01
申请号：US13489204
申请日：2012-06-05
IPC分类号： C12Q1/68
CPC分类号： C12N15/1065 , C12N15/10 , C12N15/1093 , C12P19/34 , C12Q1/6806 , C12Q1/6855 , C12Q1/6869 , C12Q1/6874 , C12Q2535/122 , C12Q2521/507
摘要： Compositions of transposome complexes for generating DNA fragments with specific 5′- and 3′-tags. Kits for generating libraries for sequencing, with transposome complexes, enzymes, oligonucleotides or other components.
摘要翻译： 用于产生具有特异性5'-和3'标签的DNA片段的转座子复合物的组合物。 用于产生用于测序的文库的试剂盒，具有转座体复合物，酶，寡核苷酸或其它组分。
-
公开(公告)号：US09080211B2
公开(公告)日：2015-07-14
申请号：US12605337
申请日：2009-10-24
CPC分类号： C12N15/1065 , C12N15/10 , C12N15/1093 , C12P19/34 , C12Q1/6806 , C12Q1/6855 , C12Q1/6869 , C12Q1/6874 , C12Q2535/122 , C12Q2521/507
摘要： The present invention provides methods, compositions and kits for using a transposase and a transposon end for generating extensive fragmentation and 5′-tagging of double-stranded target DNA in vitro, then using a DNA polymerase for generating 5′- and 3′-tagged single-stranded DNA fragments without performing a PCR amplification reaction, wherein the first tag on the 5′-ends exhibits the sequence of the transferred transposon end and optionally, an additional arbitrary sequence, and the second tag on the 3′-ends exhibits a different sequence from the sequence exhibited by the first tag. The method is useful for generating 5′- and 3′-tagged DNA fragments for use in a variety of processes, including processes for metagenomic analysis of DNA in environmental samples, copy number variation (CNV) analysis of DNA, and comparative genomic sequencing (CGS), including massively parallel DNA sequencing (so-called “next-generation sequencing.).
摘要翻译： 本发明提供了使用转座酶和转座子末端在体外产生双链靶DNA的广泛断裂和5'标记的方法，组合物和试剂盒，然后使用DNA聚合酶产生5'-和3'标记 单链DNA片段，而不进行PCR扩增反应，其中5'-末端的第一个标签显示转移的转座子末端的序列和任选的另外的任意序列，3'-末端的第二个标签显示出 与第一个标签展示的序列不同的序列。 该方法可用于产生用于各种过程的5'-和3'标记的DNA片段，包括环境样品中DNA的宏基因组分析过程，DNA拷贝数变异（CNV）分析和比较基因组测序（ CGS），包括大规模并行DNA测序（所谓的“下一代测序”）。
-
5.发明申请TRANSPOSON END COMPOSITIONS AND METHODS FOR MODIFYING NUCLEIC ACIDS 有权TRANSPOSON END COMPOSITIONS AND METHODS FOR MODIZING NUCLEIC ACIDS公开(公告)号：US20110287435A1
公开(公告)日：2011-11-24
申请号：US13177772
申请日：2011-07-07
CPC分类号： C12N15/1065 , C12N15/10 , C12N15/1093 , C12P19/34 , C12Q1/6806 , C12Q1/6855 , C12Q1/6869 , C12Q1/6874 , C12Q2535/122 , C12Q2521/507
摘要： Compositions of transposome complexes for generating DNA fragments with specific 5′- and 3′-tags. Kits for generating libraries for sequencing, with transposome complexes, enzymes, oligonucleotides or other components.
摘要翻译： 用于产生具有特异性5'-和3'标签的DNA片段的转座子复合物的组合物。 用于产生用于测序的文库的试剂盒，具有转座体复合物，酶，寡核苷酸或其它组分。
-
公开(公告)号：US09085801B2
公开(公告)日：2015-07-21
申请号：US13489204
申请日：2012-06-05
CPC分类号： C12N15/1065 , C12N15/10 , C12N15/1093 , C12P19/34 , C12Q1/6806 , C12Q1/6855 , C12Q1/6869 , C12Q1/6874 , C12Q2535/122 , C12Q2521/507
摘要： Compositions of transposome complexes for generating DNA fragments with specific 5′- and 3′-tags. Kits for generating libraries for sequencing, with transposome complexes, enzymes, oligonucleotides or other components.
-
公开(公告)号：US20110272191A1
公开(公告)日：2011-11-10
申请号：US13102029
申请日：2011-05-05
申请人： Haiying LI , William Lee Harrison
发明人： Haiying LI , William Lee Harrison
CPC分类号： H01L23/293 , C08G59/226 , C08G59/32 , C08G59/38 , C08G59/50 , C08L63/00 , C08L2666/22 , C09J163/00 , H01L2924/0002 , H01L2924/00
摘要： A potting material for an electronic component, an electronic component, and a process for positioning ferrites in an electronic material are disclosed. The potting material is formed by curing a mixture. The mixture includes an epoxy component, an organic amine hardener, a viscosity-controlling agent, and a silica. The potting material has a coefficient of thermal expansion between an inorganic ferrite coefficient of thermal expansion and an organic substrate coefficient of thermal expansion of the electronic component. The potting material includes a rigidity permitting via drilling by one or more of mechanical drilling and laser burning.
摘要翻译： 公开了一种用于电子部件的灌封材料，电子部件以及将铁氧体定位在电子材料中的工艺。 灌封材料通过固化混合物形成。 该混合物包括环氧组分，有机胺硬化剂，粘度控制剂和二氧化硅。 封装材料具有无机铁氧体热膨胀系数与电子部件的有机基板热膨胀系数之间的热膨胀系数。 灌封材料包括通过一次或多次机械钻孔和激光燃烧钻孔所允许的刚度。
-
公开(公告)号：US06570029B2
公开(公告)日：2003-05-27
申请号：US09860081
申请日：2001-05-17
申请人： Lejun Wang , Haiying Li , Ching-Ping Wong
发明人： Lejun Wang , Haiying Li , Ching-Ping Wong
IPC分类号： C07D30302
CPC分类号： H01L21/563 , C07D303/16 , C07D303/36 , C08G59/24 , C08G59/28 , C08G59/4215 , C08G59/686 , C08L63/00 , H01L23/293 , H01L2224/73203 , H01L2924/01012 , H01L2924/01019 , H01L2924/01077 , H01L2924/01087 , H01L2924/01322
摘要： A no-flow reworkable epoxy underfill is provided for use in an electronic packaged system which incorporates an integrated circuit, an organic printed wire board, and at least one eutectic solder joint formed therebetween. An exemplary embodiment of the encapsulant includes: a cycloaliphatic epoxide; an organic hardener; a curing accelerator; and a fluxing agent wherein said cycloaliphatic epoxide includes a carbonate or carbamate group. The encapsulant can also include a filler, such as a silica filler. A method is also provided for forming the aforementioned reworkable epoxy underfills.
-
9.发明申请TRANSPOSON END COMPOSITIONS AND METHODS FOR MODIFYING NUCLEIC ACIDS 有权TRANSPOSON END COMPOSITIONS AND METHODS FOR MODIZING NUCLEIC ACIDS公开(公告)号：US20140162897A1
公开(公告)日：2014-06-12
申请号：US14148463
申请日：2014-01-06
IPC分类号： C12Q1/68
CPC分类号： C12N15/1065 , C12N15/10 , C12N15/1093 , C12P19/34 , C12Q1/6806 , C12Q1/6855 , C12Q1/6869 , C12Q1/6874 , C12Q2535/122 , C12Q2521/507
摘要： The present invention provides methods, compositions and kits for using a transposase and a transposon end for generating extensive fragmentation and 5′-tagging of double-stranded target DNA in vitro, then using a DNA polymerase for generating 5′- and 3′-tagged single-stranded DNA fragments without performing a PCR amplification reaction, wherein the first tag on the 5′-ends exhibits the sequence of the transferred transposon end and optionally, an additional arbitrary sequence, and the second tag on the 3′-ends exhibits a different sequence from the sequence exhibited by the first tag. The method is useful for generating 5′- and 3′-tagged DNA fragments for use in a variety of processes, including processes for metagenomic analysis of DNA in environmental samples, copy number variation (CNV) analysis of DNA, and comparative genomic sequencing (CGS), including massively parallel DNA sequencing (so-called “next-generation sequencing.)
摘要翻译： 本发明提供了使用转座酶和转座子末端在体外产生双链靶DNA的广泛断裂和5'标记的方法，组合物和试剂盒，然后使用DNA聚合酶产生5'-和3'标记 单链DNA片段，而不进行PCR扩增反应，其中5'-末端的第一个标签显示转移的转座子末端的序列和任选的另外的任意序列，3'-末端的第二个标签显示出 与第一个标签展示的序列不同的序列。 该方法可用于产生用于各种过程的5'-和3'标记的DNA片段，包括环境样品中DNA的宏基因组分析过程，DNA拷贝数变异（CNV）分析和比较基因组测序（ CGS），包括大规模并行DNA测序（所谓的“下一代测序”）。
-
10.发明申请TRANSPOSON END COMPOSITIONS AND METHODS FOR MODIFYING NUCLEIC ACIDS 有权TRANSPOSON END COMPOSITIONS AND METHODS FOR MODIZING NUCLEIC ACIDS公开(公告)号：US20100120098A1
公开(公告)日：2010-05-13
申请号：US12605337
申请日：2009-10-24
CPC分类号： C12N15/1065 , C12N15/10 , C12N15/1093 , C12P19/34 , C12Q1/6806 , C12Q1/6855 , C12Q1/6869 , C12Q1/6874 , C12Q2535/122 , C12Q2521/507
摘要： The present invention provides methods, compositions and kits for using a transposase and a transposon end for generating extensive fragmentation and 5′-tagging of double-stranded target DNA in vitro, then using a DNA polymerase for generating 5′- and 3′-tagged single-stranded DNA fragments without performing a PCR amplification reaction, wherein the first tag on the 5′-ends exhibits the sequence of the transferred transposon end and optionally, an additional arbitrary sequence, and the second tag on the 3′-ends exhibits a different sequence from the sequence exhibited by the first tag. The method is useful for generating 5′- and 3′-tagged DNA fragments for use in a variety of processes, including processes for metagenomic analysis of DNA in environmental samples, copy number variation (CNV) analysis of DNA, and comparative genomic sequencing (CGS), including massively parallel DNA sequencing (so-called “next-generation sequencing.)
摘要翻译： 本发明提供了使用转座酶和转座子末端在体外产生双链靶DNA的广泛断裂和5'标记的方法，组合物和试剂盒，然后使用DNA聚合酶产生5'-和3'标记 单链DNA片段，而不进行PCR扩增反应，其中5'-末端的第一个标签显示转移的转座子末端的序列和任选的另外的任意序列，3'-末端的第二个标签显示出 与第一个标签展示的序列不同的序列。 该方法可用于产生用于各种过程的5'-和3'标记的DNA片段，包括环境样品中DNA的宏基因组分析过程，DNA拷贝数变异（CNV）分析和比较基因组测序（ CGS），包括大规模并行DNA测序（所谓的“下一代测序”）。
-
-
-
-
-
-
-
-
-
搜索结果
11 条记录 (耗时 0.02 秒)
