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    • 1. 发明授权
    • Stable compositions for nucleic acid amplification and sequencing
    • 用于核酸扩增和测序的稳定组合物
    • US08741560B2
    • 2014-06-03
    • US13345632
    • 2012-01-06
    • Ayoub RashtchianJoseph Solus
    • Ayoub RashtchianJoseph Solus
    • C12Q1/68C12P19/34C07H21/02C07H21/04
    • C12N9/1252C12N9/96C12P19/34C12Q1/686C12Q1/6869C12Q2527/149C12Q2527/137C12Q2527/125
    • The present invention is directed to compositions comprising mixtures of reagents, including thermostable enzymes (e.g., thermostable DNA polymerases), buffers, cofactors and other components, suitable for immediate use in nucleic acid amplification or sequencing techniques without dilution or addition of further components. The compositions contain no stabilizing agents (e.g., glycerol or serum albumin) and unexpectedly maintain activity for extended periods of time upon storage at temperatures above freezing. These compositions are useful, alone or in the form of kits, for nucleic acid amplification (e.g., by the Polymerase Chain Reaction) and sequencing (e.g., by dideoxy or “Sanger” sequencing), or for any procedure utilizing thermostable DNA polymerases in a variety of medical, forensic and agricultural applications. In particular, the compositions and methods are useful for amplifying and sequencing nucleic acid molecules that are larger than about 7 kilobases in size.
    • 本发明涉及包含试剂混合物的组合物,包括热稳定酶(例如热稳定的DNA聚合酶),缓冲液,辅因子和其它组分,适于立即用于核酸扩增或测序技术而不稀释或添加其它组分。 组合物不含稳定剂(例如甘油或血清白蛋白),并且在高于冰点的温度下储存时,意外地保持活性较长时间。 这些组合物单独或以试剂盒的形式用于核酸扩增(例如,通过聚合酶链式反应)和测序(例如,通过双脱氧或“Sanger”测序),或者对于使用热稳定性DNA聚合酶 各种医疗,法医和农业应用。 特别地,组合物和方法可用于扩增和测序尺寸大于约7千碱基的核酸分子。
    • 6. 发明申请
    • STABLE COMPOSITIONS FOR NUCLEIC ACID AMPLIFICATION AND SEQUENCING
    • 用于核酸扩增和测序的稳定组合物
    • US20120142007A1
    • 2012-06-07
    • US13345632
    • 2012-01-06
    • Ayoub RashtchianJoseph Solus
    • Ayoub RashtchianJoseph Solus
    • C12Q1/68C12P19/34C07H21/04C12N9/12
    • C12N9/1252C12N9/96C12P19/34C12Q1/686C12Q1/6869C12Q2527/149C12Q2527/137C12Q2527/125
    • The present invention is directed to compositions comprising mixtures of reagents, including thermostable enzymes (e.g., thermostable DNA polymerases), buffers, cofactors and other components, suitable for immediate use in nucleic acid amplification or sequencing techniques without dilution or addition of further components. The compositions contain no stablizing agents (e.g., glycerol or serum albumin) and unexpectedly maintain activity for extended periods of time upon storage at temperatures above freezing. These compositions are useful, alone or in the form of kits, for nucleic acid amplification (e.g., by the Polymerase Chain Reaction) and sequencing (e.g., by dideoxy or “Sanger” sequencing), or for any procedure utilizing thermostable DNA polymerases in a variety of medical, forensic and agricultural applications. In particular, the compositions and methods are useful for amplifying and sequencing nucleic acid molecules that are larger than about 7 kilobases in size.
    • 本发明涉及包含试剂混合物的组合物,包括热稳定酶(例如热稳定的DNA聚合酶),缓冲液,辅因子和其它组分,适于立即用于核酸扩增或测序技术而不稀释或添加其它组分。 组合物不含稳定剂(例如甘油或血清白蛋白),并且在高于冰点的温度下储存时,意外地保持活性延长的时间。 这些组合物单独或以试剂盒的形式用于核酸扩增(例如,通过聚合酶链式反应)和测序(例如,通过双脱氧或“Sanger”测序),或者对于使用热稳定性DNA聚合酶 各种医疗,法医和农业应用。 特别地,组合物和方法可用于扩增和测序尺寸大于约7千碱基的核酸分子。
    • 7. 发明申请
    • STABLE COMPOSITIONS FOR NUCLEIC ACID AMPLIFICATION AND SEQUENCING
    • 用于核酸扩增和测序的稳定组合物
    • US20090233283A1
    • 2009-09-17
    • US12129597
    • 2008-05-29
    • Ayoub RashtchianJoseph Solus
    • Ayoub RashtchianJoseph Solus
    • C12Q1/68C12P19/34
    • C12N9/1252C12N9/96C12P19/34C12Q1/686C12Q1/6869C12Q2527/149C12Q2527/137C12Q2527/125
    • The present invention is directed to compositions comprising mixtures of reagents, including thermostable enzymes (e.g., thermostable DNA polymerases), buffers, cofactors and other components, suitable for immediate use in nucleic acid amplification or sequencing techniques without dilution or addition of further components. The compositions contain no stabilizing agents (e.g., glycerol or serum albumin) and unexpectedly maintain activity for extended periods of time upon storage at temperatures above freezing. These compositions are useful, alone or in the form of kits, for nucleic acid amplification (e.g., by the Polymerase Chain Reaction) and sequencing (e.g., by dideoxy or “Sanger” sequencing), or for any procedure utilizing thermostable DNA polymerases in a variety of medical, forensic and agricultural applications. In particular, the compositions and methods are useful for amplifying and sequencing nucleic acid molecules that are larger than about 7 kilobases in size.
    • 本发明涉及包含试剂混合物的组合物,包括热稳定酶(例如热稳定的DNA聚合酶),缓冲液,辅因子和其它组分,适于立即用于核酸扩增或测序技术而不稀释或添加其它组分。 组合物不含稳定剂(例如甘油或血清白蛋白),并且在高于冰点的温度下储存时,意外地保持活性较长时间。 这些组合物单独或以试剂盒的形式用于核酸扩增(例如,通过聚合酶链式反应)和测序(例如,通过双脱氧或“Sanger”测序),或者对于使用热稳定性DNA聚合酶 各种医疗,法医和农业应用。 特别地,组合物和方法可用于扩增和测序尺寸大于约7千碱基的核酸分子。
    • 9. 发明授权
    • Polymerases for analyzing or typing polymorphic nucleic acid fragments and uses thereof
    • 用于分析或分型多态性核酸片段的聚合酶及其用途
    • US06306588B1
    • 2001-10-23
    • US09019160
    • 1998-02-06
    • Joseph SolusShuwei YangDeb K. Chatterjee
    • Joseph SolusShuwei YangDeb K. Chatterjee
    • C12Q168
    • C12Q1/6858C12N9/1252Y10S435/81C12Q2525/151C12Q2521/101
    • The present invention provides methods for use in identifying, analyzing and typing polymorphic DNA fragments, particularly minisatellite, microsatellite or STR DNA fragments. In particular, the invention provides methods using DNA polymerases, more particularly thermostable DNA polymerases, and most particularly Thermotoga polymerases or mutants or derivatives thereof, whereby minisatellite, microsatellite or STR DNA molecules maybe amplified and analyzed for polymorphisms. The invention also relates to polymerases having reduced, substantially reduced or eliminated ability to add non-template 3′ nucleotides to a synthesized nucleic acid molecule. In accordance with the invention, such reduction or elimination may be accomplished by modifying or mutating the desired polymerase.
    • 本发明提供了用于鉴定,分析和分型多形性DNA片段,特别是微型卫星,微卫星或STR DNA片段的方法。 特别地,本发明提供使用DNA聚合酶,更特别是耐热性DNA聚合酶的方法,最特别的是Thermotoga聚合酶或其突变体或衍生物,由此可以扩增和分析微卫星,微卫星或STR DNA分子的多态性。 本发明还涉及具有降低的,显着降低的或消除了向合成的核酸分子添加非模板3'核苷酸的能力的聚合酶。 根据本发明,可以通过修饰或突变所需的聚合酶来实现这种还原或消除。