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    • 122. 发明授权
    • Determination of lymphocyte reactivity to specific
    • 测定淋巴细胞对特异性的反应性
    • US5360719A
    • 1994-11-01
    • US954440
    • 1992-09-30
    • Robert A. LevineStephen C. Wardlaw
    • Robert A. LevineStephen C. Wardlaw
    • G01N33/50G01N33/53G01N33/569C12Q1/04G01N33/49
    • G01N33/5091G01N33/56972Y10S435/975Y10T436/25375
    • A patient's blood sample is incubated with an antigen and tested for lymphocyte response, i.e. an activation of lymphocytes and/or a conversion of lymphocytes to lymphoblasts, which indicates prior exposure of the patient to the antigen. A positive response indicates the presence of prior exposure to prior diseases or clinical conditions such as parasitic diseases, tuberculosis, salmonellosis, gonorrhea, fungal infections, rickettsial infections, Lyme disease or allergens. Whole blood from the patient is incubated with the antigen of the disease or condition for which the patient is being tested. After a suitable time, a fluorescent dye or colorant which has an affinity for a discriminant characteristic of the activated lymphocytes or lymphoblasts, such as: intracellular calcium; surface activation antigens such as transferrin receptor; HLA-Dr; Leu-23; and the like. The incubated blood is then drawn into a transparent tube containing a float which concentrates the buffy coat constituent layers upon centrifugation of the blood sample. The concentrated lymphocyte layer is then examined for fluorescence or coloration which is indicative of the presence of the activated lymphocytes or lymphoblasts, and their concentration. The fluorescence or coloration can be qualified and/or quantified by a reader instrument.
    • 将患者的血液样品与抗原一起孵育并测试淋巴细胞反应,即淋巴细胞的激活和/或淋巴细胞向淋巴母细胞的转化,其指示患者事先暴露于抗原。 阳性反应表明先前接触先前疾病或临床病症如寄生虫病,结核病,沙门氏菌病,淋病,真菌感染,立克次体感染,莱姆病或过敏原。 将来自患者的全血与患者正在测试的疾病或病症的抗原一起温育。 在合适的时间之后,对活化的淋巴细胞或淋巴母细胞的鉴别特征具有亲和力的荧光染料或着色剂,例如:细胞内钙; 表面活化抗原如转铁蛋白受体; HLA-Dr; Leu-23; 等等。 然后将孵育的血液吸入含有浮子的透明管中,该浮子在血液样品离心时浓缩血沉棕黄层组成层。 然后检查浓缩的淋巴细胞层的荧光或着色,其指示活化的淋巴细胞或淋巴母细胞的存在及其浓度。 荧光或着色可由阅读器仪器进行鉴定和/或定量。
    • 130. 发明授权
    • Standard for calibrating and/or verifying instrument accuracy
    • 用于校准和/或验证仪器精度的标准
    • US4141654A
    • 1979-02-27
    • US799178
    • 1977-05-23
    • Stephen C. WardlawRobert A. Levine
    • Stephen C. WardlawRobert A. Levine
    • B01L3/00B01L3/14G01N21/27G02B27/32G01C25/00
    • B01L3/561B01L3/5021G02B27/32G01N21/278
    • A device for use in checking and/or calibrating the accuracy with which a blood constituent concentration measuring instrument is operating. The device includes a capillary tube size member having annular bands marked on its outer surface. The bands are of predetermined axial extent and simulate centrifuged blood cell or other constituent layers. The axial dimension of each band is measured on the instrument which provides a visual indication of corresponding blood cell count. The blood cell count indicated by the instrument is then compared to the known blood count corresponding to the predetermined axial extent of the particular band measured. This device may be used to calibrate the instrument or determine the accuracy with which the instrument is operating.
    • 用于检查和/或校准血液成分浓度测量仪器正在操作的精度的装置。 该装置包括在其外表面上标记有环形带的毛细管尺寸构件。 条带具有预定的轴向范围,并模拟离心血细胞或其他构成层。 在仪器上测量每个带的轴向尺寸,其提供相应血细胞计数的视觉指示。 然后将由仪器指示的血细胞计数与对应于所测量的特定带的预定轴向范围的已知血液计数进行比较。 该设备可用于校准仪器或确定仪器运行的准确性。