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    • 4. 发明授权
    • Method for detecting analytes
    • 检测分析物的方法
    • US08691595B2
    • 2014-04-08
    • US12666024
    • 2008-06-20
    • Andreas BergmannJoachim Struck
    • Andreas BergmannJoachim Struck
    • G01N33/549
    • G01N33/54306
    • The subject of this invention is a process for detection of analytes from biological samples comprising the following process steps: a) Preparation of a reversible binding partner 1 that is immobilized on a solid phase, to which an analyte binder is reversibly bonded via a reversible binding partner 2 that is bonded to the analyte binder, whereby the analyte binder is immobilized by binding between the reversible binding partners 1 and 2, b) Addition of the biological sample and binding of the analyte to the reversible immobilized analyte binder in the case that the biological sample contains the analytes, c) Separation of the biological sample, d) Addition of a dissolving buffer, which dissolves the binding between the reversible binding partners 1 and 2, whereby the binding of the analyte to the analyte binder remains optional, and e) Detection of the analyte in the dissolving buffer in the case that the biological sample contains the analytes and determination of the absence of the analyte in the case that the biological sample does not contain the analytes, respectively.
    • 本发明的主题是用于检测来自生物样品的分析物的方法,包括以下过程步骤:a)固定在固相上的可逆结合配偶体1的制备,分析物粘合剂通过可逆结合可逆地结合到其上 配偶体2,其结合到分析物粘合剂上,由此通过可逆结合配偶体1和2之间的结合固定分析物粘合剂,b)添加生物样品并将分析物与可逆固定的分析物结合物结合, 生物样品含有分析物,c)生物样品的分离,d)加入溶解缓冲液,其溶解可逆结合配偶体1和2之间的结合,由此分析物与分析物质粘合剂的结合仍然是可选的,e )在生物样品含有分析物和确定不存在分析物的情况下,检测溶解缓冲液中的分析物 在生物样品不分别含有分析物的情况下分析物。
    • 8. 发明授权
    • In vitro procedure for diagnosis and early diagnosis of neurodegenerative diseases
    • 诊断和早期诊断神经变性疾病的体外方法
    • US08298784B2
    • 2012-10-30
    • US12300747
    • 2007-05-15
    • Andreas BergmannAndrea ErnstHarald Hampel
    • Andreas BergmannAndrea ErnstHarald Hampel
    • G01N33/53G01N33/537G01N33/567
    • G01N33/6896G01N2800/28
    • An in vitro process for the detection and early detection of neurodegenerative diseases, for determination of the severity, and to evaluate the progression of and render a prognoses of neurogenerative diseases, in a patient suffering from a subjectively or objectively detectable cognitive impairment, by determining the concentration of an analyte selected from natriuretic peptides, in particular ANP, and, if necessary, BNP and/or CNP in a biological fluid of the patient, whereby the determination of the analyte is performed directly and/or indirectly as the determination of a relevant co-peptide generated from a mutual propeptide, and is based upon the measured concentration of the determined analyte thus making it possible to form conclusions about a neurodegenerative disease or an early form typical of such a disease or the course of the disease and/or the success of the efforts to relieve or prevent the disease.
    • 一种用于检测和早期检测神经变性疾病,用于确定严重程度并评估患有主观或客观可检测的认知障碍的患者中神经生殖疾病的进展和预测神经生殖疾病的体外方法,通过确定 选自利尿钠肽,特别是ANP的分析物的浓度,以及如果需要,BNP和/或CNP在患者的生物液体中的浓度,由此分析物的测定直接和/或间接地作为相关的测定 由相互前肽产生的共肽,并且基于所测定的分析物的测量浓度,从而可以形成关于神经变性疾病或这种疾病典型的早期形式或疾病过程和/或 成功地减轻或预防疾病的努力。