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World File Search SystemAmplification
GE Medical Systems SCS C/O Peter Uhlir监管事务...
BD Probetec Trichomonas阴道/IS（TV）Q'扩增DNA分析（TVQ分析）基于使用放大引物和荧光标记的探测器探针的同时扩增和检测靶DNA。The reagents for SDA are dried in two separate disposable microwells: the Priming Microwell contains the amplification primers, fluorescently-labeled detector probe, nucleotides and other reagents necessary for amplification, while the Amplification Microwell contains the two enzymes (a DNA polymerase and a restriction endonuclease) that are required for SDA.BD Viper T R M系统移液管从每个提取管中纯化的DNA溶液中的一部分进入底漆的微孔，以补充含量。短暂孵育后，将反应混合物转移到相应的，预热的放大微孔中，该放大微孔被密封以防止污染，然后在两种热能控制LED LED荧光读取器之一中孵育。通过计算峰值荧光（在扩增过程中最大的相对荧光单元（MAXRFU））来确定毛果素丝虫阴道/IS DNA的存在或不存在。
α-突触核蛋白种子扩增测定法检测到疾病后期常染色体显性阿尔茨海默氏病中的路易体共介术，并依赖于路易病理学负担
授予/奖励号：U19AG032438;国家老化研究所；阿尔茨海默氏症协会，赠款/奖励号：SG-20-690363-DIAN LATAM；德国神经退行性疾病中心；劳尔·卡雷（Raul Carrea）神经研究所；痴呆症的研发赠款；日本医学研发机构；韩国痴呆研究中心，赠款/奖励号：HU21C0066；西班牙卫生研究院卡洛斯三世；加拿大卫生研究所；加拿大神经退行性和衰老联盟，大脑加拿大基金会； BMBF-德国研究和教育部，赠款/奖励号：（FKZ，FKZ161L0214B，FKZ161L0214CCLINSPECT-M）；德国研究基金会在慕尼黑系统神经病学框架内的德国卓越策略（Synergy），赠款/奖励号：exc2145Synergy -ID390857198
认可的考试程序DIN EN ISO 17025：...
Clostridium perfringens Enterotoxin gene DNA, quantitative microbiology amplification of pathogen diagnostics / quantitative PCR SOP-T-367 2 Clostridium perfringens toxin net-gen-DNA, qualitative microbiology amplification excitement diagnosis / Real Time PCR / DNA SOP-T-367 2 Clostridium perfringens toxin nete-gen-DNA, quantitative激发诊断 /定量PCR SOP-T-367的微生物学放大2灌注裂齿轮毒素毒素NETF-GEN-DNA，定性微生物学扩增激发诊断 /实时PCR / DNA SOP / DNA SOP / DNA SOP / DNA SOP / DNA SOP / DNA SOP / DNA SOP-T-T-367 2梭状芽胞杆菌量化量子 /量子量化量子量，定量量化微生物学量化微生物学量化量子学量化量化量化量化， SOP-T-367 2Clostridium perfringens Enterotoxin gene DNA, quantitative microbiology amplification of pathogen diagnostics / quantitative PCR SOP-T-367 2 Clostridium perfringens toxin net-gen-DNA, qualitative microbiology amplification excitement diagnosis / Real Time PCR / DNA SOP-T-367 2 Clostridium perfringens toxin nete-gen-DNA, quantitative激发诊断 /定量PCR SOP-T-367的微生物学放大2灌注裂齿轮毒素毒素NETF-GEN-DNA，定性微生物学扩增激发诊断 /实时PCR / DNA SOP / DNA SOP / DNA SOP / DNA SOP / DNA SOP / DNA SOP / DNA SOP-T-T-367 2梭状芽胞杆菌量化量子 /量子量化量子量，定量量化微生物学量化微生物学量化量子学量化量化量化量化， SOP-T-367 2
第12章：聚合酶链反应（PCR）概述
Amplification of DNA for: • Sequencing • Genotyping • Cloning • Pathogen detection Advantages • Increased dynamic range of detection • No post-PCR processing • Higher sensitivity and specificity • Closed system reduces the risk of contamination • An increase in reporter fluorescent signal is directly proportional to the number of amplicons generated • Shorter turnaround time • No post-PCR processing
分子生物学和基因工程课程
1.1 Extraction et purification de l'ADN ............................................................................. 49 1.2 Fragmentation ............................................................................................................... 49 1.3 Séparation analytique .................................................................................................... 50 1.4 Visualisation ................................................................................................................. 50 1.5 Quantification ............................................................................................................... 51 1.6 Hybridization and microarrays ............................................................................................... 52 1.7 Amplification (PCR and its applications) ......................................................................................................................................................................................................................................................................................................................................................................................................................................................... ............................................................................................................... 58 Chapter I.sources and preparation of DNA to clone ....................................................... 58
α-突触核蛋白种子扩增测定法检测到疾病后期常染色体显性阿尔茨海默氏病中的路易体共介术，并依赖于路易病理学负担
授予/奖励号：U19AG032438;国家老化研究所；阿尔茨海默氏症协会，赠款/奖励号：SG-20-690363-DIAN LATAM；德国神经退行性疾病中心；劳尔·卡雷（Raul Carrea）神经研究所；痴呆症的研发赠款；日本医学研发机构；韩国痴呆研究中心，赠款/奖励号：HU21C0066；西班牙卫生研究院卡洛斯三世；加拿大卫生研究所；加拿大神经退行性和衰老联盟，大脑加拿大基金会； BMBF-德国研究和教育部，赠款/奖励号：（FKZ，FKZ161L0214B，FKZ161L0214CCLINSPECT-M）；德国研究基金会在慕尼黑系统神经病学框架内的德国卓越策略（Synergy），赠款/奖励号：exc2145Synergy -ID390857198
开发CDK2选择性的小分子抑制剂...
Primary resistance: About 15% of patients treated with CDK4/6 inhibitor (CDK4/6i) + aromatase inhibitor, and up to 30% of those treated with CDK4/6i + fulvestrant, will develop recurrent disease within 6 months Acquired resistance: Almost all patients will eventually develop progressive disease Multiple pathways are implicated in resistance CCNE1 amplification and cyclin E1 overexpression are
病毒学申请表
Adenovirus Qualitative/Semi-Quantitative* CT/GC Combo NAAT ( Nucleic Acid Amplification) Adenovirus Types 40 & 41 Trichomonas NAAT Astrovirus Retrovirology (HIV-1, HIV-2) BK Virus Quantitative - For Prognosis/Monitoring of Positive Patients Bordetella pertussis HIV-1 RNA Quantitative NAAT( Nucleic Acid Amplification ) For监测/预后弯曲杆菌sp。冠状病毒229E *冠状病毒NL63 *血清学 - 抗体/抗原测试冠状病毒OC43 *冠状病毒HKU1 *巨细胞病毒（CMV）定性 - 用于诊断H. pylori抗原CMV数量的诊断 - 用于预测/肠胃肠病患者的诊断（用于预测的肠胃）（促进）的静态（促进）（促进）的预测型（促进）（均为预测）艰难的毒素A＆B（无棉签）爱泼斯坦 - 巴尔病毒（EBV）定性 - 用于诊断细菌学培养EBV定量 - 用于预后/监测阳性患者人类疱疹病毒6（HHV -6）定性 - 用于诊断血液体液的抑制性HHV -6尿液素毒性 - 用于诊断性HHV -6的抑制作用，以进行预后炎 -