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    • 4. 发明授权
    • Limited volume method and apparatus for particle counting
    • 有限体积法和粒子计数装置
    • US4739171A
    • 1988-04-19
    • US789994
    • 1985-10-22
    • Jonathan Briggs
    • Jonathan Briggs
    • G01N21/64G01N33/542G01T1/10
    • G01N33/542G01N21/6428G01N2201/08
    • A method and apparatus for determining the presence of particles in a fluorescent dispersion which exceed either a predetermined fluorescence intensity or size are disclosed. The method and apparatus involve the irradiation of the dispersion with excitation light, the examination of the fluorescent light entering an optical fiber from a portion of the excited region small enough to permit only a low probability that more than one particle of interest is present in the volume during a predetermined period of time, and the measurement of the emitted fluorescence entering the fiber, substantially free of excitation light, to the extent that the fluorescence differs in intensity from that of the dispersion in the absence of the particle.
    • 公开了一种用于确定荧光分散体中超过预定荧光强度或尺寸的颗粒的存在的方法和装置。 该方法和装置包括用激发光照射分散体,从激发区域的一部分进入光纤的荧光的检查小到足以允许仅有一个以上感兴趣的颗粒存在的可能性低 在预定时间段内的体积,以及基本上不含激发光的进入纤维的发射荧光的测量,使得在不存在颗粒的情况下荧光的强度与分散体的强度不同。
    • 5. 发明授权
    • Solid-state optical assay imaging apparatus
    • 固态光学测定成像装置
    • US4737464A
    • 1988-04-12
    • US780485
    • 1985-09-26
    • Harden M. McConnellJonathan BriggsJohn W. Parce
    • Harden M. McConnellJonathan BriggsJohn W. Parce
    • G01N21/25G01N21/27G01N21/00
    • G01N21/253G01N21/272G01N21/6428G01N2201/0461Y10S436/805Y10S436/807Y10T436/11
    • An apparatus for determining a characteristic of a signal modulating component related to an analyte of interest at an assay site by measuring light modulated by the component. A light source uniformly illuminates the assay site and a reference site. The light is directed from the sites onto a group of memory cells on the surface of a random access memory. The memory cells will decay from a logical 1 to a logical 0 due to the light over a period of time which is a function of the intensity of the light and the reference voltage of the memory cells marking the difference between a 1 and a 0. The digital state of each of the memory cells in the group is measured a predetermined exposure time. The measured states of a group of memory cells corresponding to the assay site are compared to the memory cell states for a reference group. The measured states are then analyzed to determine a characteristic of the analyte.
    • 一种用于通过测量由该组分调制的光来确定在测定部位与感兴趣分析物相关的信号调节成分的特征的装置。 光源均匀地照射了测定部位和参考部位。 光从站点引导到随机存取存储器表面上的一组存储器单元上。 存储器单元将由于在一段时间内的光而从逻辑1衰减到逻辑0,该时间段是光的强度和记录单元的参考电压的函数,标记1和0之间的差。 在预定的曝光时间内测量组中的每个存储单元的数字状态。 将对应于测定位点的一组存储器单元的测量状态与参考组的存储器单元状态进行比较。 然后分析测量的状态以确定分析物的特征。
    • 6. 发明授权
    • Method of sequencing nucleic acids by shift registering
    • 通过移位登记测序核酸的方法
    • US6043036A
    • 2000-03-28
    • US977931
    • 1997-11-24
    • Randy M. McCormickJonathan Briggs
    • Randy M. McCormickJonathan Briggs
    • C12Q1/68C12P19/34
    • C12Q1/6869G06F19/22
    • The present invention describes a method of sequencing nucleic acids in which mixtures of oligonucleotide fragments are derived from sequencing reactions using combinations of the 2',3'-dideoxynucleoside 5'-triphosphate or 3' deoxynucleoside 5'-triphosphate terminators and appropriate concentrations of four dNTPs (2'-deoxynucleoside 5' triphosphates, e.g., dATP, dCTP, dGTP, dTTP, dITP, 7-deaza-GTP). These fragments are generated by enzymatic extension of a primer hybridized to the single-stranded template DNA to be sequenced. In contrast to common slab gel sequencing methods, the method of the instant invention does not require precise alignment of the four separation sets of the terminated fragments to permit deduction of the DNA sequence. In addition, the method possesses inherent redundancy in the separations, which facilitates sequence assignment by resolving sequence uncertainties or anomalies.
    • 本发明描述了使用2',3'-双脱氧核苷5'-三磷酸终止子和3'脱氧核苷5'-三磷酸终止子的组合以及合适浓度的4个核苷酸的序列来测序核酸的方法,其中寡核苷酸片段的混合物来源于测序反应 dNTPs(2'-脱氧核苷5'三磷酸,例如dATP,dCTP,dGTP,dTTP,dITP,7-脱氮-GTP)。 这些片段通过与要测序的单链模板DNA杂交的引物的酶促延伸产生。 与普通平板凝胶测序方法相反,本发明的方法不需要对终止的片段的四个分离组进行精确的比对以允许推断DNA序列。 此外,该方法在分离中具有固有的冗余性,这有助于通过解析序列不确定性或异常来进行序列分配。