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    • 161. 发明授权
    • Detection and quantification of one or more target analytes in a sample using spatially localized analyte reproduction
    • 使用空间定位的分析物繁殖来检测和定量样品中一种或多种目标分析物
    • US06518038B1
    • 2003-02-11
    • US09728826
    • 2000-11-28
    • Stephen C. WardlawStephen C. Edberg
    • Stephen C. WardlawStephen C. Edberg
    • C12Q104
    • G01N33/569Y02A50/59
    • The presence or absence of one or more target microbial analytes in a substance, such as a biological or environmental substance, is assayed by inoculating a growth medium with a sample of the substance. The medium may be combined with a labeled analyte-specific material (LASM) which can migrate through the substrate and which is homogeneously distributed throughout the medium. The LASM may be premixed with the medium, or may be added to the medium after inoculation with the substance. The nature of the medium is such that it will support target analyte reproduction so as to form target analyte colonies in or on the medium, and it will not allow the target analyte colonies to migrate on or within the medium. After the sample to be assayed is added to the medium, growth of the target analyte colonies in the sample will bind increasing quantities of the LASM, thereby creating localized intensely labeled areas in the medium which can be visually or photometrically detected. As the target analyte colonies grow on or in the medium they attract increasing quantities of the LASM which diffuses to the colonies through the medium causing the local target analyte colonies to become intensely labeled, which renders the colonies readily detectable. Each of the intensely labeled target analyte colonies in the medium may also be surrounded by areas of lower intensity due to local depletion of the LASM in the regions of colony growth. The number of intensely labeled target analyte colonies in the medium will be proportional to the concentration of the target analyte present in the sample. In the event that the target analyte is absent from the sample, then there will be no localized labeled microbe colonies in the medium.
    • 通过用物质样品接种生长培养基来测定物质如生物或环境物质中的一种或多种目标微生物分析物的存在或不存在。 介质可以与标记的分析物特异性材料(LASM)组合,其可以迁移穿过基底并且均匀分布在整个介质中。 LASM可以与培养基预混合,或者可以在接种物质后添加到培养基中。 培养基的性质使得其将支持靶分析物繁殖,以便在培养基中或培养基上形成靶分析物菌落,并且不允许靶分析物菌落在培养基上或培养基内迁移。 将待测定样品加入到培养基中后,样品中目标分析物菌落的生长将结合增加量的LASM,从而在培养基中产生局部强烈标记的区域,可以在视觉上或光度上检测。 当目标分析物菌落在培养基上或培养基中生长时,它们吸引越来越多的LASM,其通过培养基扩散到菌落,导致局部目标分析物菌落变得强烈标记,这使得菌落易于检测。 由于LASM在集落生长区域局部消耗,所以介质中每个强烈标记的目标分析物菌落也可能被较低强度的区域包围。 培养基中强烈标记的目标分析物菌落的数量将与样品中存在的目标分析物的浓度成比例。 在样品中不存在目标分析物的情况下,培养基中不存在局部标记的微生物菌落。
    • 165. 发明授权
    • Method and apparatus for selectively admixing reagents in a substantially undiluted biologic fluid sample analysis
    • 在基本未稀释的生物液体样品分析中选择性混合试剂的方法和装置
    • US09322835B2
    • 2016-04-26
    • US13077251
    • 2011-03-31
    • Stephen C. Wardlaw
    • Stephen C. Wardlaw
    • G01N1/10G01N31/00G01N35/02G01N1/14G01N35/00
    • G01N35/025G01N1/14G01N35/00584G01N35/026Y10T436/2575
    • A biologic fluid sample analysis method and system is provided that includes a reagent depository, and analysis chamber, a biologic fluid transfer system, and a programmable analyzer. The reagent depository has a plurality of reagent deposits, and each reagent deposit located at a position within the depository independent of the other reagent deposits. The analysis chamber is adapted to quiescently hold a biologic fluid sample and one or more reagents during analysis. The biologic fluid transfer system has at least one fluid transfer device. The programmable analyzer is adapted to control the biologic fluid transfer system to acquire a volume of sample from a sample reservoir, dispense a volume of the sample into the reagent depository, acquire a volume of sample and reagent from the reagent depository, and to transfer the sample and reagent to the analysis chamber, and to analyze the combined sample and reagent.
    • 提供了一种生物液体样品分析方法和系统,其包括试剂库和分析室,生物流体转移系统和可编程分析仪。 试剂库具有多个试剂沉积物,每个试剂沉积物位于存储体内的位置,而与其它试剂沉积物无关。 分析室适于在分析期间静止地保持生物流体样品和一种或多种试剂。 生物液体输送系统具有至少一个流体转移装置。 可编程分析仪适用于控制生物流体转移系统,以从样品储存器获取一定体积的样品,将样品的体积分配到试剂储存器中,从试剂库获取一定体积的样品和试剂,并将 样品和试剂分析到分析室,并分析组合的样品和试剂。
    • 169. 发明申请
    • BUFFY COAT SEPARATOR FLOAT SYSTEM AND METHOD
    • BUFFY COAT SEPATATOR FLOAT SYSTEM AND METHOD
    • US20120164683A1
    • 2012-06-28
    • US13371761
    • 2012-02-13
    • Thomas HaubertVince ContiniSteve GrimesRandy JonesStephen C. Wardlaw
    • Thomas HaubertVince ContiniSteve GrimesRandy JonesStephen C. Wardlaw
    • C12Q1/04B29C45/00C12M1/34
    • B01L3/50215Y10T436/111666Y10T436/25375
    • A tube and float system for use in separation and axial expansion of the buffy coat includes a transparent or semi-transparent, flexible sample tube and a rigid separator float having a specific gravity intermediate that of red blood cells and plasma. The float includes a main body portion of reduced diameter to provide a clearance gap between the inner wall of the sample tube and the float. One or more protrusions on the main body portion serve to support the flexible tube. During centrifugation, the centrifugal force causes the diameter of the flexible tube to expand and permit density-based axial movement of the float in the tube. The float further includes a pressure relief system to alleviate pressure build up in the trapped red blood cell blood fraction below the float, thereby preventing red blood cells from being forced into the annular gap containing the buffy coat layers.
    • 用于血沉棕黄层的分离和轴向膨胀的管和浮子系统包括透明或半透明的柔性样品管和具有红细胞和血浆的比重中间体的刚性分离器浮子。 浮子包括直径减小的主体部分,以在样品管的内壁和浮子之间提供间隙。 主体部分上的一个或多个突起用于支撑柔性管。 在离心过程中,离心力使柔性管的直径膨胀并允许管中的浮子的基于密度的轴向运动。 浮子还包括一个压力释放系统,以减轻在浮子下面的被捕获的红细胞血液部分中的压力增加,从而防止红细胞被迫进入含有血沉棕黄层的环形间隙。
    • 170. 发明申请
    • BUFFY COAT TUBE AND FLOAT SYSTEM AND METHOD
    • US20110171680A1
    • 2011-07-14
    • US13052151
    • 2011-03-21
    • Thomas HaubertStephen C. Wardlaw
    • Thomas HaubertStephen C. Wardlaw
    • C12Q1/02C12M1/00
    • B01L3/505B01L3/50215B01L2400/0409G01N33/49Y10S435/81Y10S436/81
    • A tube and float system for use in separation and axial expansion of the buffy coat is provided. The system includes a transparent, or semi-transparent, flexible sample tube and a rigid separator float having a specific gravity intermediate that of red blood cells and plasma. The sample tube has an elongated sidewall having a first cross-sectional inner diameter. The float consists of a main body portion and one or more support members protruding from the main body portion to engage and support the sidewall of the sample tube. The main body portion and the support members of the float have a cross-sectional diameter less than that of the first cross-sectional inner diameter of the tube when the sample tube is expanded, such as by centrifugation. The main body portion of the float together with an axially aligned portion of the sidewall define an annular volume therebetween. The support members protruding from the main body portion of the float traverse said annular volume to produce one or more analysis areas. During centrifugation, the centrifugal force enlarges the diameter of the tube to permit density-based axial movement of the float in the tube. Thereafter, the centrifugal force is reduced to cause the tube sidewall to return to its first diameter, thereby capturing the float and trapping the buffy coat constituents in the analysis area. The bully coat constituents can then be evaluated or measured.
    • 提供了用于分离和轴向膨胀血沉棕黄层的管和浮子系统。 该系统包括透明或半透明的柔性样品管和具有红细胞和血浆的比重中间体的刚性分离器浮子。 样品管具有具有第一横截面内径的细长侧壁。 浮子包括主体部分和从主体部分突出的一个或多个支撑构件,以接合和支撑样品管的侧壁。 例如通过离心,浮体的主体部分和支撑构件的横截面直径小于管的第一截面内径的横截面直径。 浮子的主体部分与侧壁的轴向对准部分在其间限定了环形体积。 从浮子的主体部分突出的支撑构件穿过所述环形体积以产生一个或多个分析区域。 在离心过程中,离心力扩大了管的直径,以允许管中的浮子的基于密度的轴向运动。 此后,减小离心力使管侧壁回到其第一直径,从而捕获浮子并将分析区域中的血沉棕黄层成分捕获。 然后可以评估或测量欺负涂层成分。