厌氧菌培养
- 网络Anaerobic Culture
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啤酒厌氧菌培养基的选择
Choice of Beer Anaerobic Culture Medium
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通过收集临床标本并与厌氧菌培养进行比较,验证此体系的特异性、敏感性和临床应用可行性。
Collection of clinical specimens and compared with anaerobic culture , and detection simulated specimen verify the specificity , sensitivity and feasibility of clinical application of this system .
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人精浆、厌氧菌培养液在HSV-2诱导宫颈癌中的作用
Effect of Human Semen and Anaerobic Bacteria Culture Fluid on Induction of Cervical Carcinoma in mice
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方法:将新鲜消毒的中厚猪皮、尸体皮和经过-80℃降温,LN2冻存的猪皮、尸体皮各取6块行需氧菌和厌氧菌培养,而后做细菌学检测。
Methods : We took 6 pieces each of fresh and disinfected intermediate thickness pig-skin and corpse-skin and - 80 ℃ / LN 2 frozen stored pig-skin and corpse-skin for aerobic bacteria and anaerobic bacteria cultivation , then carried out bacteriology examination .
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方法:采集正畸过程中的龈沟液进行厌氧菌培养。
Method : The crevicular fluids were cultured in anaerobic condition .
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心脏手术后病人血及其引流血经需氧菌及厌氧菌培养均阴性。
Anaerobic and aerobic cultures of the shed mediastinal blood were negative .
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感染根管的厌氧菌培养结果分析
Analyses on the Results of Anaerobic Bacteria Culture in the Infected Root-Canals
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20颗用氢氧化钙药尖消毒为对照组,消毒前后分别作需氧菌和厌氧菌培养并比较其消毒效果。
20 with calcium hydroxide medicine points as control group .
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胎膜破裂前后羊水及脐血厌氧菌培养68例分析
Anaerobic culture of amniotic fluid and umbilical cord blood before
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方法:需氧菌和厌氧菌培养以及药物敏感试验。
Methods : Culture and drug sensitivity test of aerobic bacteria and anaerobic bacteria .
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子宫颈炎的厌氧菌培养结果分析
Result analysis of anaerobic bacterial culture in cervicitis
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正常人眼结膜囊的厌氧菌培养
Anaerobic Flora of the Normal Human Conjunctival Sac
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微波消毒根管前后的需氧菌和厌氧菌培养;
Fostering of aerobe and anaerobe before and after root canal sterilization with microwave .
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一种简易有效的厌氧菌培养装置
The Simple and Effective Anaerobic Culture Device
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厌氧菌培养及其抗生素敏感性试验
Anaerobic cultivation and drug sensitivity tests
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荧光抗体法及厌氧菌培养法检出类杆菌与梭状杆菌的质量控制
The Quality Control of Immunofluorescent Antibody Test and Anaerobic Culture in Study of Bacteroides and Fusobacterium
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腹部感染标本厌氧菌培养的细菌学特征。
Objective to elected the bacteriology characteristic of the anaerobic bacteria culture from abdominal infections specimens .
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为了解塞条引产的安全性,在放置塞条前后取宫颈管粘液作厌氧菌培养。
Before and after insertion of the tent , cervical mucus samples were collected and cultured for anaerobes .
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通过对36例儿童龋源性牙病的厌氧菌培养,将所获的94株菌进行了种属归类。
We used anaerobic culture to 36 cases of children 's dental diseases caused by decayed teeth and classified 94 anaerobic strains .
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102个烧伤创面的厌氧菌培养,阳性率为14.7%。
Anaerobic culture was performed for 102 swab specimens from the burn wounds and a positive rate of 14.7 % was obtained .
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检出细菌3173%(33/104),但27例需氧菌及厌氧菌培养均为阴性。
Bacteria were found in 31 73 % ( 33 / 104 ), but we failed to isolate bacteria by culture in 27 cases .
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作者自制的平皿厌氧菌培养装置,阳性检出率为74%,比常用的厌氧箱和厌氧罐阳性检出率高。
The positive ratio is 74 percent using the plate anaerobe culturing device made by author , higher than using common anaerobic box and anaerobic jar .
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方法采用厌氧菌培养技术,对5~7天的32名初乳喂养儿和24名人工喂养儿的粪便做双歧杆菌和肠杆菌定量培养。
Methods Using anaerobic incubation techniques , quantitative-stool culture of bifidobacteria and enterobacteria was performed on days 5 - 7 of 32 colostrum-fed newborns and 24 bottler fed newborns .
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采用液体培养基管、半固体琼脂培养基管、无菌干空针与无菌干空管等方法同时送检厌氧菌培养标本;
Three transport systems are introduced , the liquid and semisolid agar medium tubes and the sterilized dry aerobic syringe , comparing with that of the sterilized dry aerobic tube for culture of anaerobic bacteria .
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方法:采用厌氧菌连续培养技术,用菌液的吸光度(ABS)和菌落计数作指标,描述矿化液对变链菌生长繁殖的影响;
METHODS : Continuous anaerobic cultivating technique and describing its effects on propagate of Streptococcus mutans with absorbency ( ABS ) of bacterial liquid and take count of bacteria .
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巯基醋酸盐液体培养基主要用于厌氧菌的培养。
Fluid Thioglycollate Medium is primarily intended for the culture of anaerobic bacteria .
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产气荚膜梭菌和腐败梭菌在厌氧菌基础培养基中的生长特性
Characters Growth of Cl. perfringens and Cl. Septicum Cultivated in the Basic Medium of Anaerobic Bacteria
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对啤酒发酵中的厌氧菌的培养测定方法进行了探讨。
Culture and determination methods were give a discussion about anaerobic bacterium of the beer fementation .
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结果在厌氧菌液体培养基中加入低聚果糖前后双歧杆菌菌数分别为1.5亿/ml和3亿/ml;
Results The number of Bifidobacteria in the anaerobic liquid medium with and without oligofructose was 300 and 150 million / ml respectively .
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将工作菌液采用涂抹法接种于营养琼脂培养基和厌氧菌琼脂培养基,置厌氧条件35℃培养,用未接种的培养基做空白对照。
Inoculated the above working bacterial suspension into the nutrient agar medium and anaerobic bacterium agar medium with daubing method and incubated them under anaerobic condition at 35 ℃, and used the culture medium without inoculated as control .