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    • 2. 发明申请
    • RECOVERY IMMUNOASSAY FOR THE SIMULTANEOUS IMMUNOCHEMICAL DETERMINATION OF AN ANALYTE (ANTIGEN) AND A TREATMENT ANTIBODY TARGETING THE ANALYTE
    • RECOVERY IMMUNOASSAY用于同时免疫化学测定中的分析物(抗原)和一个相对分析物靶向治疗抗体
    • WO2012059083A3
    • 2012-06-28
    • PCT/DE2011001912
    • 2011-11-01
    • BIOTEZ BERLIN BUCH GMBHSTROHNER PAVELSTAATZ ANTONIA
    • STROHNER PAVELSTAATZ ANTONIA
    • G01N33/68G01N33/564
    • G01N33/6854G01N33/564
    • The invention relates to an immunoassay for the simultaneous immunochemical determination of an analyte (antigen) and a treatment antibody, treatment antibody modification, or treatment antibody analog (TAB) targeting the analyte (recovery immunoassay). The immunoassay according to the invention comprises: an optionally marked capture antibody, capture antibody modification, or capture antibody analog (CAB) bound to a surface, a marked treatment antibody, a marked treatment antibody modification, or a marked treatment antibody analog (TABmarked) or a marked antibody that has the same binding epitope or the same binding domain as the treatment antibody, or the treatment antibody modification or treatment antibody analog (TAB) used for treatment, in a mixture with an excess of the unmarked treatment antibody, treatment antibody modification, or treatment antibody analog (TAB), an antigen, which binds with the capture antibody, capture antibody modification, or capture antibody analog (CAB) and the treatment antibody, treatment antibody modification, or treatment antibody analog (TAB) at various epitopes and thus forms an immunochemical sandwich, a solvent of the unmarked treatment antibody, treatment antibody modification, or treatment antibody analog (TAB) of known concentration, and an antigen solution to be added to the samples. Areas of application of the invention are medical diagnostics, treatment control, and pharmacological research.
    • 本发明涉及一种用于同时测定的免疫化学分析物(抗原)的免疫测定和针对分析物的抗体疗法,或Therapieantikörpersmodifikats-analogs(TAB)(恢复免疫测定)。 本发明的免疫测定法包括:结合到表面任选标记的捕获抗体,Fängerantikörpermodifikat或 - 模拟(CAB)的部分,具有显着的治疗性抗体,标记的Therapieantikörpermodifikat或 - 模拟(TABmarkiert)或相同的标记抗体,相同的结合表位,或 结合结构域,如抗体治疗,或具有Therapieantikörpermodifikat用于治疗或 - 模拟(TAB),混合有一个过量的未标记的治疗性抗体或Therapieantikörpermodifikats-analogs(TAB),抗原(与捕获抗体,Fängerantikörpermodifikat或 - 模拟 CAB)和TAB)结合治疗性抗体,或Therapieantikörpermodifikat - 模拟(在由此形成的已知Konze的夹层免疫化学,未标记的抗体疗法中的溶液,或Therapieantikörpermodifikats-analogs(TAB)的不同表位 并添加抗原溶液以补充样品。 本发明的应用领域是医学诊断,治疗控制和药理学研究。
    • 4. 发明申请
    • METHOD OF MARKING BIOMOLECULES USING HORSERADISH PEROXIDASE
    • 程序用于标记生物分子辣根过氧化物酶
    • WO1997024618A1
    • 1997-07-10
    • PCT/DE1996002511
    • 1996-12-24
    • BIOTEZ BERLIN-BUCH GMBHSCHMIDT, EberhardWEISS, Christa
    • BIOTEZ BERLIN-BUCH GMBH
    • G01N33/532
    • G01N33/535G01N2333/908Y10S435/964
    • The invention concerns a method for the enzymatic marking of biomolecules, including peptides, hormones, antibodies and other haptens, using horseradish peroxidase (HRP). Instead of uncontrolled formation of heterogenous coupling products, the method proposed calls for the enzyme to be oxidized by sodium metaperiodate and then cross-linked intermolecularly in controlled fashion, using some of the aldehyde groups formed by the oxidation, with an alpha , omega -diaminoalkane, preferably 1,13-diamino-4,7,10-trioxatridecane. This produces an aggregate, made up of 6 to 10 HRP molecules, to which the protein to be marked can be coupled, without previously separating it from the reaction mixture, via the remaining aldehyde groups. An advantage of HRP cross-linking in this way is that a higher degree of substitution can be obtained. Since the protein is not hidden behind HRP molecules, it can exert its immunological properties without any restriction and can be determined without error using spectrophotometric techniques. The sensitivity and specificity of the HRP tracer obtained is extremely high and quite comparable to that of radioactive tracers. The HRP marking method proposed thus represents a remarkable advance in the development of high-performance enzymatic immunological detection systems.
    • 本发明涉及一种新方法,酶促生物分子,包括肽,激素,抗体或其他半抗原的标记,与辣根过氧化物酶(HRP)。 代替不受控制的形成的异构偶合产物的是通过本发明的方法通过在受控的方式偏高碘酸钠氧化酶第一分子间通过利用与α,ω-二氨基烷烃形成的醛基团的一部分,优选1,13-二氨基-4,7- ,10三氧烷,网络化。 从而聚合产生,其由6至10个HRP分子要被标记的蛋白质被耦合,而不脱离在剩余的醛基反应混合物之前分离。 正如在前面的HRP交联的一个优点是说,具有高取代度可以实现的。 因为蛋白质不受HRP分子屏蔽,其可以非限制性地发挥其免疫学性质和是无差错的分光光度测量。 所得HRP示踪剂的灵敏度和特异性是可比非常高和放射性示踪剂。 这代表了新的HRP标记过程代表的高性能发展的显着的进步酶免疫学检测系统。
    • 5. 发明申请
    • RECOVERY IMMUNOASSAY ZUR GLEICHZEITIGEN IMMUNCHEMISCHEN BESTIMMUNG EINES ANALYTEN (ANTIGEN) UND EINES GEGEN DEN ANALYTEN GERICHTETEN THERAPIEANTIKÖRPERS
    • RECOVERY IMMUNOASSAY用于同时免疫化学测定中的分析物(抗原)和一个相对分析物靶向治疗抗体
    • WO2012059083A2
    • 2012-05-10
    • PCT/DE2011/001912
    • 2011-11-01
    • BIOTEZ BERLIN-BUCH GMBHSTROHNER, PavelSTAATZ, Antonia
    • STROHNER, PavelSTAATZ, Antonia
    • G01N33/68
    • G01N33/6854G01N33/564
    • Die Erfindung bezieht sich auf einen Immunoassay zur gleichzeitigen immunchemischen Bestimmung eines Analyten (Antigen) und eines gegen den Analyten gerichteten Therapieantikörpers, Therapieantikörpersmodifikats oder -analogs (TAB) (Recovery Immunoassay). Der erfindungsgemäße Immunoassay umfasst: einen an einer Oberfläche gebundenen gegebenenfalls markierten Fängerantikörper, Fängerantikörpermodifikat bzw. -analog (CAB), einen markierten Therapieantikörper, ein markiertes Therapieantikörpermodifikat oder -analog (TABmarkiert) oder einen markierten Antikörper, der das gleiche Bindungsepitop, bzw. die gleiche Bindungsdomaine wie der Therapieantikörper, bzw. das zur Therapie eingesetzte Therapieantikörpermodifikat oder -analog (TAB) aufweist, im Gemisch mit einem Überschuss des unmarkierten Therapieantikörpers, Therapieantikörpermodifikats oder -analogs (TAB), ein Antigen, das mit dem Fängerantikörper, Fängerantikörpermodifikat oder -analog (CAB) und dem Therapieantikörper, Therapieantikörpermodifikat oder -analog (TAB) an verschiedenen Epitopen bindet und dadurch einen immunochemischen Sandwich bildet, eine Lösung des unmarkierten Therapieantikörpers, Therapieantikörpermodifikats oder -analogs (TAB) bekannter Konzentration und eine Antigenlösung zur Aufstockung der Proben. Anwendungsgebiete der Erfindung sind die medizinische Diagnostik, die Therapiekontrolle und die pharmakologische Forschung.
    • 本发明涉及一种用于同时测定的免疫化学分析物(抗原)的免疫测定和针对分析物的抗体疗法,或Therapieantikörpersmodifikats-analogs(TAB)(恢复免疫测定)。 本发明的免疫测定法包括:结合到表面任选标记的捕获抗体,Fängerantikörpermodifikat或 - 模拟(CAB)的部分,具有显着的治疗性抗体,标记的Therapieantikörpermodifikat或 - 模拟(TABmarkiert)或相同的标记抗体,相同的结合表位,或 结合结构域,如抗体治疗,或具有Therapieantikörpermodifikat用于治疗或 - 模拟(TAB),混合有一个过量的未标记的治疗性抗体或Therapieantikörpermodifikats-analogs(TAB),抗原(与捕获抗体,Fängerantikörpermodifikat或 - 模拟 CAB)和TAB)结合治疗性抗体,或Therapieantikörpermodifikat - 模拟(在由此形成的已知Konze的夹层免疫化学,未标记的抗体疗法中的溶液,或Therapieantikörpermodifikats-analogs(TAB)的不同表位 ntration和用于分配的抗原溶液到样品中。 本发明的应用是医学诊断,治疗控制和药理学研究。
    • 7. 发明申请
    • METHOD FOR IDENTIFYING SINGLE NUCLEOTIDE POLYMORPHISMS (SNP) IN GENES WHICH METABOLIZE MEDICAMENTS AND TEST KIT FOR CARRYING OUT SAID METHOD
    • METHOD FOR单核苷酸多态性毒品和代谢试验试剂盒用于实施所述方法的基因检测(SNP)
    • WO2004018707A2
    • 2004-03-04
    • PCT/DE0302699
    • 2003-08-07
    • BIOTEZ BERLIN BUCH GMBHNEUNABER RALFSTROHNER PAVELSCHREIBER JOACHIMVOIGT GESINESCHUNCK WOLF-HAGEN
    • NEUNABER RALFSTROHNER PAVELSCHREIBER JOACHIMVOIGT GESINESCHUNCK WOLF-HAGEN
    • C12Q1/68
    • C12Q1/6858C12Q2565/518C12Q2563/131C12Q2535/125C12Q2535/131
    • The invention relates to a simplified method for identifying SNP in human cytochrome P450 (CYP) genes and to a test kit comprising the following components: 1. Novel synthetic oligonucleotides, suitable for amplifying gene segments in genes that metabolize medicaments, with the aid of isoform-specific (IS-PCR) DNA polymerase chain reaction technology (PCR), from genomic leukocyte DNA, 2. Components enabling the selective, thermostable, single-stranded immobilization of biotinated IS-PCR products on microplates coated with streptavidin (SA-MTP), 3. Test optimized, allele-specific, fluorescein isothiocyanate (FITC) labeled synthetic oligonucleotides, which guarantee a reliable genotyping of the immobilized amplification products (amplicons), by hybridization, subsequent stringent washing and finally detection using fluorometry or photometry, or alternatively 4. Streptavidin coated glass object carrier (SA chip), on which biotinated, isoform-specific, synthetic oligonucleotides are immobilized, which are hybridized with partially single-stranded PCR products that have been produced by a discriminatory extension of an allele-specific, terminally FITC labeled oligonucleotide using Taq DNA Polymerase and which guarantee a reliable genotyping of the immobilized amplicons by subsequent stringent washing and finally detection using fluorometry or photometry. In comparison with the known high-throughput method, said invention enables clinical findings, which are of therapeutic importance for an individual provision of the different CYP alleles, to be established at low cost in terms of personnel and resources, even for small numbers of individual patients.
    • 本发明涉及一种用于在细胞色素P450(CYP)的人力和测试试剂盒具有以下组分的基因检测的SNP的简化方法:1.新开发的合成寡核苷酸,其能够基因序列中使用“DNA聚合酶药物代谢的基因 链式反应“(PCR)技术isoformspezifisch(IS-PCR)从基因组白细胞DNA扩增,第二部件,其允许在链亲和素包被微量滴定板(SA-MTP)的单链生物素化的IS-PCR产物选择性地加热稳定的和单链,以 固定3.测试优化的,等位基因特异性,异硫氰酸荧光素(FITC)标记的通过杂交保证,随后严格洗涤和随后的检测合成的寡核苷酸通过irrmobilisierten扩增产物(扩增子),或可替代地,链霉4.荧光BESC和光度测量的可靠的基因分型 hichtete载玻片(SA-Chip)的生物素化在其上,同种型,合成的寡核苷酸被固定,其杂交与Taq DNA聚合酶的手段通过等位基因特异性,末端FITC标记寡核苷酸的歧视性扩展生成部分单链PCR产物,并通过随后的严格性洗涤和 确保荧光和光度测量杂交扩增可靠的检测分型。 在与已知的“高通量”过程使本文所描述的本发明,并且在几个个别患者低劳动力和材料成本上升的等位基因,所述治疗重要发现单个设备与各种CYP。
    • 9. 发明授权
    • VERFAHREN ZUR MARKIERUNG VON BIOMOLEKÜLEN MIT MEERRETTICHPEROXIDASE
    • 程序用于标记生物分子辣根过氧化物酶
    • EP0877938B2
    • 2004-04-21
    • EP96946118.5
    • 1996-12-24
    • Biotez Berlin-Buch GmbH
    • SCHMIDT, EberhardWEISS, Christa
    • G01N33/532G01N33/535
    • G01N33/535G01N2333/908Y10S435/964
    • The invention concerns a method for the enzymatic marking of biomolecules, including peptides, hormones, antibodies and other haptens, using horseradish peroxidase (HRP). Instead of uncontrolled formation of heterogenous coupling products, the method proposed calls for the enzyme to be oxidized by sodium metaperiodate and then cross-linked intermolecularly in controlled fashion, using some of the aldehyde groups formed by the oxidation, with an α,φ-diaminoalkane, preferably 1,13-diamino-4,7,10-trioxatridecane. This produces an aggregate, made up of 6 to 10 HRP molecules, to which the protein to be marked can be coupled, without previously separating it from the reaction mixture, via the remaining aldehyde groups. An advantage of HRP cross-linking in this way is that a higher degree of substitution can be obtained. Since the protein is not hidden behind HRP molecules, it can exert its immunological properties without any restriction and can be determined without error using spectrophotometric techniques. The sensitivity and specificity of the HRP tracer obtained is extremely high and quite comparable to that of radioactive tracers. The HRP marking method proposed thus represents a remarkable advance in the development of high-performance enzymatic immunological detection systems.