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    • 4. 发明申请
    • Method for quantification of biological material in a sample
    • 用于定量样品中生物材料的方法
    • US20070065894A1
    • 2007-03-22
    • US11526147
    • 2006-09-21
    • Andrew CroteauMark PiersonDavid TownsendAli Naqui
    • Andrew CroteauMark PiersonDavid TownsendAli Naqui
    • C12Q1/34C12M3/00
    • B01L3/5088B01L3/5085B01L3/50853B01L2300/0803C12M23/12C12M23/20C12M23/22C12M23/38C12M25/14C12M35/08C12M37/00C12M41/36C12Q1/24
    • Methods for the detection and/or quantification of a biological material in a sample. The method includes the steps of liquefying the sample (if necessary) and pouring the liquefied sample into the incubation vessel. The incubation vessel has a generally flat horizontal surface and the surface is divided into at least one incubation site. Each incubation site is adapted to hold an aliquot of liquid and is sized and shaped, and formed of a suitable material, to hold the aliquot within the well by surface tension. Any excess liquid from the liquefied sample is poured from the surface of the incubation vessel. The method then involves incubating that incubation vessel until the presence or absence of the biological material is determined. The presence of air bubbles can be dramatically reduced by the presence of a surface acting agent in the liquid sample deposited on the device surface. Such an agent can be added to the sterile diluent used to prepare the test reagent, can be separately added to the test reagent after it is prepared, or can be added to the test sample directly while it is being prepared for testing.
    • 用于检测和/或定量样品中生物材料的方法。 该方法包括如下步骤:将样品液化(如有必要)并将液化的样品倒入培养容器中。 培养容器具有大致平坦的水平表面,并且将表面分成至少一个孵育位点。 每个孵化位点适于保持液体的等分试样,并且其尺寸和形状由合适的材料形成,以通过表面张力将等分试样保持在孔内。 从培养容器的表面倒出来自液化样品的任何多余的液体。 然后,该方法包括孵育该培养容器,直到确定生物材料的存在或不存在。 通过在沉积在器件表面上的液体样品中存在表面作用剂,可以显着降低气泡的存在。 可以将这样的试剂加入用于制备测试试剂的无菌稀释剂中,可以在制备试剂后分别添加到试验试剂中,或者可以在制备试剂时直接加入试验样品中。
    • 7. 发明授权
    • Method for quantification of biological material in a sample
    • 用于定量样品中生物材料的方法
    • US07122338B2
    • 2006-10-17
    • US10349196
    • 2003-01-21
    • Andrew J. CrouteauMark W. PiersonDavid E. TownsendAli Naqui
    • Andrew J. CrouteauMark W. PiersonDavid E. TownsendAli Naqui
    • C12Q1/24
    • B01L3/5088B01L3/5085B01L3/50853B01L2300/0803C12M23/12C12M23/20C12M23/22C12M23/38C12M25/14C12M35/08C12M37/00C12M41/36C12Q1/24
    • Methods for the detection and/or quantification of a biological material in a sample. The method includes the steps of liquefying the sample (if necessary) and pouring the liquefied sample into the incubation vessel. The incubation vessel has a generally flat horizontal surface and the surface is divided into at least one incubation site. Each incubation site is adapted to hold an aliquot of liquid and is sized and shaped, and formed of a suitable material, to hold the aliquot within the well by surface tension. Any excess liquid from the liquefied sample is poured from the surface of the incubation vessel. The method then involves incubating that incubation vessel until the presence or absence of the biological material is determined. The presence of air bubbles can be dramatically reduced by the presence of a surface acting agent in the liquid sample deposited on the device surface. Such an agent can be added to the sterile diluent used to prepare the test reagent, can be separately added to the test reagent after it is prepared, or can be added to the test sample directly while it is being prepared for testing.
    • 用于检测和/或定量样品中生物材料的方法。 该方法包括如下步骤:将样品液化(如有必要)并将液化的样品倒入培养容器中。 培养容器具有大致平坦的水平表面,并且将表面分成至少一个孵育位点。 每个孵化位点适于保持液体的等分试样,并且其尺寸和形状由合适的材料形成,以通过表面张力将等分试样保持在孔内。 从培养容器的表面倒出来自液化样品的任何多余的液体。 然后,该方法包括孵育该培养容器,直到确定生物材料的存在或不存在。 通过在沉积在器件表面上的液体样品中存在表面作用剂,可以显着降低气泡的存在。 可以将这样的试剂加入用于制备测试试剂的无菌稀释剂中,可以在制备试剂后分别添加到试验试剂中,或者可以在制备试剂时直接加入试验样品中。
    • 9. 发明授权
    • Method for immunoassay using lactoperoxidase, starch and iodine
    • 使用乳过氧化物酶,淀粉和碘的免疫测定方法
    • US5166054A
    • 1992-11-24
    • US636800
    • 1991-01-02
    • Ali Naqui
    • Ali Naqui
    • C12Q1/28G01N33/58
    • G01N33/581C12Q1/28
    • A method for immoassay includes a membrane coated with a capture antibody and starch. A solution suspected of containing an antigen is passed through the membrane. Antigen binds to the capture antibody. A conjugate of a detection antibody and lactoperoxidase is passed through the membrane to form a sandwich on the membrane. A substrate composition including peroxide and iodide is passed through. The lactoperoxidase catalyzes oxidation of iodide by the peroxide to give iodine which reacts with the starch to give a blue color. The invention includes a kit of materials for performing the assay of the invention.
    • 非免疫测定方法包括涂覆有捕获抗体和淀粉的膜。 怀疑含有抗原的溶液通过膜。 抗原结合捕获抗体。 检测抗体和乳过氧化物酶的缀合物通过膜以在膜上形成三明治。 包含过氧化物和碘化物的底物组合物通过。 乳过氧化物酶催化由过氧化物氧化碘化物,得到与淀粉反应的碘,得到蓝色。 本发明包括用于进行本发明测定的一组材料。
    • 10. 发明授权
    • Method and apparatus for concurrently detecting pathogenic organisms and antimicrobial susceptibility
    • 同时检测病原菌和抗菌药物敏感性的方法和装置
    • US06984499B2
    • 2006-01-10
    • US08942369
    • 1997-10-02
    • Chun-Ming ChenCharles R. CarpenterHaoyi GuAli Naqui
    • Chun-Ming ChenCharles R. CarpenterHaoyi GuAli Naqui
    • C12Q1/04C12Q1/18
    • C12Q1/20C12Q1/08
    • The present invention relates to a method of detecting the presence of target microorganisms in a biological sample and of simultaneously determining the susceptibility of the microorganisms to antimicrobial agents. The target microbial organisms may be urinary pathogens. The methods include the steps of providing a multicompartment assay device with at least one compartment containing a medium capable of sustaining the growth of total viable microorganisms, at least one compartment containing a medium capable of sustaining the growth of target microorganisms, and at least one compartment containing an antimicrobial susceptibility interpretation medium. A biological sample is placed in each compartment and the presence and antimicrobial susceptibility of the target microorganisms which may be present is determined by analyzing which compartments exhibit microbial growth.
    • 本发明涉及一种检测生物样品中目标微生物的存在并同时测定微生物对抗微生物剂的敏感性的方法。 目标微生物可能是尿病原体。 所述方法包括以下步骤:提供具有至少一个隔室的步骤,所述隔室包含能够维持总存活微生物生长的培养基,至少一个含有能够维持靶微生物生长的培养基的隔室,以及至少一个室 含有抗微生物敏感性解释培养基。 将生物样品置于每个隔室中,通过分析哪些隔室呈现微生物生长来确定可能存在的目标微生物的存在和抗微生物敏感性。