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AmpliSensor—聚合酶链反应定量检测肺结核患者外周血结 …
引用本文:谭耀驹,李一耕.AmpliSensor—聚合酶链反应定量检测肺结核患者外周血结 …[J].中华结核和呼吸杂志,1999,22(8):481-483.
作者姓名:谭耀驹  李一耕
作者单位:广州市胸科医院肺部疾病研究所
摘    要:目的 探讨AmpliSensor-聚合酶链反应定量检测外周血中结核分支杆菌DNA在肺结核的应用价值。方法 采用QlAamp和AcuPure法提取,制备全血中模板TB-DNA,应用AmpliSensor-PCR定量检测,并与IS6110-单管巢式聚合酶链反应(SN-PCR)作比较。结果200例肺结核患者的血液标本中,两种方法测得结核分支杆菌DNA的阳性率分别为60.5%、63.5%。85例非结核肺病

关 键 词:聚合酶链反应  肺结核  结核分支杆菌  DNA

Quantitative detection of Mycobacterium tuberculosis DNA in peripheral blood from patients with pulmonary tuberculosis by AmpliSensor PCR technique
TAN Yaoju,LI Yigeng,ZHANG Yanbin,et al Pulmonary Disease Institute,Guangzhou Chest Hospital,Guangzhou.Quantitative detection of Mycobacterium tuberculosis DNA in peripheral blood from patients with pulmonary tuberculosis by AmpliSensor PCR technique[J].Chinese Journal of Tuberculosis and Respiratory Diseases,1999,22(8):481-483.
Authors:TAN Yaoju  LI Yigeng  ZHANG Yanbin  Pulmonary Disease Institute  Guangzhou Chest Hospital  Guangzhou
Institution:Pulmonary Disease Institute, Guangzhou Chest Hospital, Guangzhou 510095.
Abstract:Objective To evaluate the clinical value of the quantitative detection of Mycobacterium tuberculosis DNA by Amplisensor PCR in peripheral blood from patients with pulmonary tuberculosis Methods The model of Mycobacterium tuberculosis DNA in blood was made by QIAamp and AcuPure methods, quantitative detection of Mycobacterium tuberculosis DNA by AmpliSensor PCR technique and the results were compared with IS6110 single tube nested PCR (SN PCR) Results The peripheral blood from 200 patients with pulmonary tuberculosis were detected respectively by using AmpliSensor PCR and IS6110 SN PCR methods The positive rates of Mycobacterium tuberculosis DNA were 60 5% and 63 5% respectively, and that from 85 patients with non pulmonary tubeculosis were 4 7%, 8 2% Conclusions AmpliSensor PCR method showed higher sensitivity and specificity in detecting the Mycobacterium tubeculosis DNA from peripheral blood The variation of the TB DNA may be useful in evaluating the prognosis of the patients
Keywords:Polymerase chain reaction    Tuberculosis  pulmonary    Mycobacterium tuberculosisgate the double time of CAOV3 for 2  77 and  1  94  times  respectively    After treated by HCPT or topotecan  SKOV3 generated DNA Ladder    Positive rates of TUNE
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