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
    • 1. 发明申请
    • SEPARATION DEVICE COMPRISING A PHYSICAL BARRIER
    • 包含物理障碍物的分离装置
    • US20100264099A1
    • 2010-10-21
    • US12742386
    • 2007-11-26
    • Peter WarthoePer Berdén
    • Peter WarthoePer Berdén
    • B01D35/28B01D37/00
    • B01L3/502753B01L2300/0681B01L2300/16B01L2400/0406
    • The present invention relates to a device for separating a suspension into a liquid phase and a retentate phase. The device comprises a separation chamber comprising an application zone and a hydrophilic filter material. The separation chamber is connected to a first capillary channel, where the connecting junction between the separation chamber and the first capillary channel comprise a physical barrier preventing flow of residue retentate from a lower part of the chamber into the first capillary channel. The invention further relates to a method for separating a liquid sample consisting of less than 200 μl suspension, into a retentate phase comprising the suspended matter, and a liquid phase substantially free of suspended matter.
    • 本发明涉及一种用于将悬浮液分离成液相和滞留相的装置。 该装置包括分离室,其包括施加区域和亲水性过滤材料。 分离室连接到第一毛细通道,其中分离室和第一毛细管通道之间的连接结包括物理屏障,防止残余物滞留物从腔室的下部流入第一毛细通道。 本发明还涉及将由少于200μl悬浮液组成的液体样品分离成包含悬浮物的滞留相和基本上不含悬浮物的液相的方法。
    • 8. 发明申请
    • TECHNIQUE COMBINING PCR AND LOOP-MEDIATED ISOTHERMAL AMPLIFICATION FOR THE DETECTION OF NUCLEIC ACIDS
    • 用于检测核酸的技术组合PCR和环介导的同位素放大
    • US20150126382A1
    • 2015-05-07
    • US14400717
    • 2013-05-13
    • Peter WARTHOE
    • Peter Warthoe
    • C12Q1/68
    • C12Q1/686C12Q1/6853C12Q1/689C12Q1/6895C12Q2525/301C12Q2531/119C12Q2600/16
    • The present invention relates to a method and a kit of parts for detecting the presence or absence of one or more target nucleic acid sequences in a sample, the method comprising a sequence of steps for pre-amplifying the sample by means of a polymerase chain reaction, followed by a sequence of steps comprising an isothermal amplification of the pre-amplified sample, wherein the isothermal amplification comprises a pair of primers comprising a forward primer having a 3′ part that is substantially complementary to a first part of the target sequence, the presence or absence of which is to be detected, and a 5′ part that is substantially homolog to a second part of the target sequence, and a reverse primer comprising a 3′ part that is substantially homolog to a fourth part of the target sequence and a 5′ part that is substantially complementary to a third part of the target sequence.
    • 本发明涉及一种用于检测样品中一种或多种靶核酸序列的存在或不存在的部分的方法和试剂盒,所述方法包括通过聚合酶链反应预扩增样品的步骤序列 之后是包括预扩增样品的等温扩增的步骤序列,其中等温扩增包括一对引物,其包含具有与靶序列的第一部分基本上互补的3'部分的正向引物, 其目标序列的第二部分基本上同源的5'部分和与靶序列的第四部分基本相同的3'部分的反向引物,和 5'部分,其与目标序列的第三部分基本互补。
    • 9. 发明申请
    • BIO SURFACE ACOUSTIC WAVE (SAW) RESONATOR AMPLIFICATION WITH NANOPARTICLES FOR DETECTION OF A TARGET ANALYTE
    • 用于检测目标分析仪的纳米颗粒的生物表面声波(SAW)谐振器放大
    • US20100105079A1
    • 2010-04-29
    • US12451611
    • 2008-06-02
    • Peter Warthoe
    • Peter Warthoe
    • G01N33/53
    • G01N33/54373
    • The present invention relates generally to a signal amplification method for a SAW resonator microsensor for analyzing test samples, containing target analyte including proteins and nucleic acids. The method comprising the steps: reacting the analyte in a sample with a first molecular recognition component and a second molecular recognition component linked to at least one nanoparticle; and adding an enhancement solution comprising silver ions and/or gold ions, and a reducing agent, whereby the silver ions and/or gold ions are reduced to metallic silver and/or gold which is deposited onto the surface of the at least one nanoparticle; wherein the mass increase of the at least one nanoparticle is detected by a SAW sensor.
    • 本发明一般涉及用于分析测试样品的SAW谐振器微传感器的信号放大方法,其中包含目标分析物包括蛋白质和核酸。 该方法包括以下步骤:将样品中的分析物与连接至至少一种纳米颗粒的第一分子识别组分和第二分子识别组分反应; 以及添加包含银离子和/或金离子的增强溶液和还原剂,由此将银离子和/或金离子还原成沉积在至少一种纳米颗粒的表面上的金属银和/或金; 其中所述至少一种纳米颗粒的质量增加由SAW传感器检测。
    • 10. 发明授权
    • Method for improved reverse transcription at high temperatures
    • 在高温下改进逆转录的方法
    • US06271004B1
    • 2001-08-07
    • US09603185
    • 2000-06-26
    • Peter Warthoe
    • Peter Warthoe
    • C12P1934
    • C12Q1/686C12Q2563/119C12Q2527/125C12Q2521/107
    • The invention relates to a method for enzyme stabilization. A method for improved reverse transcription at high temperatures is provided, wherein a thermostable heat shock protein (HSPs) stabilizes a reverse transcriptase, as well as reduces the RNase H activity of said reverse transcriptase. The present invention thus relates to a stabilizing agent, that prevents thermal denaturing and enhances thermostability of a reverse transcriptase. The invention further relates to a method of producing a polypeptide complex consisting of a Chaperonin and a Moloney murine leukemia virus (MMVL) reverse transcriptase, characterized by having enhanced thermostability as well as reduced RNase H activity, compared to a (MMVL) reverse transcriptase alone. The invention further relates to a kit for the preparation of cDNA from mRNA, comprising either both stabilizing agent and reverse transcriptase or the polypeptide complex of the invention.
    • 本发明涉及一种酶稳定的方法。 提供了一种在高温下改善逆转录的方法,其中热稳定热休克蛋白(HSP)稳定逆转录酶,并降低所述逆转录酶的RNA酶H活性。 因此,本发明涉及防止热变性并提高逆转录酶的热稳定性的稳定剂。 本发明进一步涉及与单独的(MMVL)逆转录酶相比,由伴侣蛋白和莫洛尼鼠白血病病毒(MMVL)逆转录酶组成的多肽复合物的方法,其特征在于具有增强的热稳定性以及降低的RNA酶H活性 。 本发明还涉及用于从mRNA制备cDNA的试剂盒,其包含稳定剂和逆转录酶两者或本发明的多肽复合物。