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   标记编码 的翻译结果: 查询用时:0.367秒
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标记编码
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  “标记编码”译为未确定词的双语例句
     With the rule of the protocol encoding, the process of the realization of the BACnet protocol is carefully discussed by the sequence of BACnet tag encoding, data type encoding, application layer user data encoding, application layer and the other layers under it control information encoding.
     根据BACnet标准协议栈编码的主要规则,按照BACnet标记编码,数据类型编码,应用层用户数据部分编码,应用层及其下各层控制信息部分编码的顺序,详细讲述了BACnet标准的具体实现工作。
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     So distance-marking method is proposed in the dissertation, which is a variable-to-fixed-length code scheme. Not only compression ratio of the method is high, but also communication protocol is simple and decompression hardware overhead is low.
     针对这个问题,本文提出了变长—定长的距离标记编码压缩方法,这种方法不仅数据压缩效率高,而且通讯协议简单,解压电路硬件开销小。
短句来源
     DNA encoding a heat-stable enterotoxin of Escherichia coli was label ledby two-step nicktranslation with Bio-11 -dUTP residues. The biotinylated DNA probe was highly specific for the detection of Enterotoxigenic Escherichia coli when reacted with protein-and RNA-free DNA in a colony hybridization assay.
     采用二步法缺口翻译反应,用Bio-11-dUTP标记编码大肠杆菌耐热肠毒素的DNA片段作为杂交探针,通过菌落杂交试验,在严格去蛋白和RNA的条件下,表明生物素标记的DNA探针对产肠毒素性大肠杆菌的检测具有高度特异性.
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  相似匹配句对
     GISH analysis demonstrated that two E.
     标记E.
短句来源
     A Research on the Performance of the Regional Code Label Switching Network
     区域编码标记交换网络性能的研究
短句来源
     DEAD MAN'S MARK(Ⅰ)
     死者的标记(上)
短句来源
     3. entropy coding.
     熵编码
短句来源
     1 encoding for RAS and call signalling messages.
     1编码;
短句来源
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  mark encoding
Biphase mark encoding is used as an appropriate compromise between the conflicting demands of high channel efficiency and low systematic jitter.
      
With standard two-channel biphase mark encoding, there is a fundamental ambiguity in the phase of the recovered clock.
      
  label coding
This training algorithm is completely supervised because each category is associated with a unique label coding for it.
      


DNA encoding a heat-stable enterotoxin of Escherichia coli was label ledby two-step nicktranslation with Bio-11 -dUTP residues. The biotinylated DNA probe was highly specific for the detection of Enterotoxigenic Escherichia coli when reacted with protein-and RNA-free DNA in a colony hybridization assay. As little as 1.25pg of target DNA can be visualized using dot blot hybridization procedure in conjunction with streptavidin and biotinylated alkaline phosphatase. The DNA hybridization assay with biotinylated...

DNA encoding a heat-stable enterotoxin of Escherichia coli was label ledby two-step nicktranslation with Bio-11 -dUTP residues. The biotinylated DNA probe was highly specific for the detection of Enterotoxigenic Escherichia coli when reacted with protein-and RNA-free DNA in a colony hybridization assay. As little as 1.25pg of target DNA can be visualized using dot blot hybridization procedure in conjunction with streptavidin and biotinylated alkaline phosphatase. The DNA hybridization assay with biotinylated DNA probe is efficient for detection of Enterotoxigenic Escherichia coli.

采用二步法缺口翻译反应,用Bio-11-dUTP标记编码大肠杆菌耐热肠毒素的DNA片段作为杂交探针,通过菌落杂交试验,在严格去蛋白和RNA的条件下,表明生物素标记的DNA探针对产肠毒素性大肠杆菌的检测具有高度特异性.用链亲和素和生物素-碱性磷酸酶系统,通过点杂交试验可以检测出1.25pg的靶序列DNA.

DNA fragment encoding a heat-stable enterotoxin of Escherichin coli was labelled with Bio-11-dUTP and used as a gene probe. Three kinds of food, meat, egg and milk were artificially contaminated with enterotoxigenic Escherichia coli, which were diluted in varying ratios and inoculated on LB agar with nitrocellulose filter membrane. After incubation for 6-10 h at 37℃and strict deletion treatment of protein and RNA, the colony hybridization was performed for detecting and counting the contaminated enterotoxigenic...

DNA fragment encoding a heat-stable enterotoxin of Escherichin coli was labelled with Bio-11-dUTP and used as a gene probe. Three kinds of food, meat, egg and milk were artificially contaminated with enterotoxigenic Escherichia coli, which were diluted in varying ratios and inoculated on LB agar with nitrocellulose filter membrane. After incubation for 6-10 h at 37℃and strict deletion treatment of protein and RNA, the colony hybridization was performed for detecting and counting the contaminated enterotoxigenic E. coli with the biotinylated DNA probe. The results indicated that the probe is highly specific and its sensitivity is 100 cells/g.

将人工污染产ST大肠杆菌的鲜猪肉、鸡蛋和牛乳稀释液接种到铺在LB琼脂表面的硝酸纤维素膜上,经37℃6~10h培养和严格的去蛋白和RNA处理后,用生物素标记的编码大肠杆菌耐热肠毒素的DNA片段作为基因探针,检测了污染食品中的产ST大肠杆菌.本法具有高度特异性,其敏感性为100个细菌/g.

 
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