glucuronidase造句
例句与造句
- Distribution of - glucuronidase activity in macaca mulatta tissues
葡糖醛酸酶在恒河猴组织中的分 - Fig . 2 the changes of myocardial beta - glucuronidase of rats after 4000 - 4500m running on treadmill . * p < 0 . 05 compared with control group
图2运动后大鼠心肌组织葡萄糖醛酸酶活力的动态变化。运动后即刻组酶活力显著增高，运动后3小时组和运动后24小时组酶活力进一步增高。 - To investigate the molecular basis of the stresses - induced gene regulation , the acbadh promoter - / ? - glucuronidase chimeric gene constructs containing six deletions were introduce into tobacco by agrobacterium - mediated transformation
对启动子进行6禾缺夫构建，瞬时转化烟草叶片表明， 6种构建都有活性。 - Microbiology of food and animal feeding stuffs - horizontal method for the enumeration of - glucuronidase - positive escherichia coli - colony - count technique at 44 c using 5 - bromo - 4 - chloro - 3 - indolyl - d - glucuronide
食品和动物饲料的微生物学.葡糖苷酸酶阳性大肠杆菌计数的水平方法. 44下用5溴- 4氯3吲哚- - d葡糖苷酸的菌落记数技术 - In transgenic tobacco plants , the analysis of transient expression by monitoring 3 - glucuronidase activity revealed that a chimeric gene construct containing a 1 . 2 kb pdf1 . 2 promoter fused to a gus reporter gene was induced by meja
( 1 )从拟南芥基因组中扩增出长度约为1200bp的pdf1 . 2启动子，与gus构建的融合基因在烟草中的表达受meja诱导。 - It's difficult to find glucuronidase in a sentence. 用glucuronidase造句挺难的
- Microbiology of food and animal feeding stuffs - horizontal method for the enumeration of - glucuronidase - positive escherichia coli - colony - count technique at 44 c using membranes and 5 - bromo - 4 - chloro - 3 - indolyl - d - glucuronide
食品和动物饲料的微生物学.葡糖苷酸酶阳性大肠杆菌计数的水平方法. 44下用隔膜和5溴- 4氯3吲哚- - d葡糖苷酸的菌落记数技术 - Microbiology of food and animal feeding stuffs - horizontal method for the enumeration of b - glucuronidase - positive escherichia coli - part 2 : colony - count technique at 44 oc using 5 - bromo - 4 - chloro - 3 - indolyl b - d - glucuronate
食品和动物饲料的微生物学. b -葡糖苷酸-阳性大肠杆菌计数的水平方法.第2部分: 44时使用5 -溴代- 4 -氯- 3 -吲哚b - d -葡糖苷酸的计群技术 - Microbiology of food and animal feeding stuffs - horizontal method for the enumeration of beta - glucuronidase positive escherichia coli using 5 - bromo - 4 - chloro - 3 - indolyl beta - d - glucuronide by colony count technique at 44 oc - routine method
食物和动物饲料的微生物学. 44时通过菌落计数法用5 -溴- 4 -氯- 3 -吲哚- d -葡糖苷酸对-葡糖苷酸酶阳性大肠杆菌计数的水平法.常规法 - Microbiology of food and animal feeding stuffs - horizontal method for the enumeration of b ? ta - glucuronidase positive escherichia coli - part 1 : colony - count technique at 44 o c using membranes and 5 - bromo - 4 - chloro - 3 - indolyl beta - d - glucoronide
食品和动物饲料的微生物学. -葡糖苷酸酶阳性大肠杆菌计数的水平方法.第1部分: 44时用薄膜材料和5 -溴代- 4氯- 3 -吲哚基- d -葡糖苷酸的菌落计数技术 - Agobacterium tumefaciens strain a311 carrying the plant tranfer vector pb1121 , which contains the neomycin phosphotransferasell gene ( nptll ) and p - glucuronidase reporter gene ( gus ) both under the control of the camv 35s promoter , was used in the establishment of the genetic tranformation of white clover
选用苗龄4 5天的带柄子叶作为外植体，先将外植体预培2天，再与根癌农杆菌a311共培养3 4天后，转入附加有40mg l ~ ( - 1 )卡那霉素和400mg - We clone a 1 . 3kb promoter sequence of the homologous gene in arabidopsis by pcr . this promoter is shown to direct the specific expression of the reporter gene , b - glucuronidase ( gus ) , in trichomes of arabidopsis . promoter deletion analysis reveal that the region from - 300 - - 1 bp is sufficient to direct trichome - specific expression
对其进行缺失突变，构建5个缺失表达载体转基因拟南芥，叶片gus定量测定分析表明- 300bp ? - 1bp序列就可以指导gus基因在表皮毛细胞中特异表达，说明这段序列可能含有指导此启动子在拟南芥表皮毛细胞进行特异表达的核心序列。 - Furthermore , by inserting " anther box " element to the mutated area of two site - mutation promoters , another two promoters , ipmas and ipmal , were created . in order to study the chemical - inducible capacity of wild and modified pr - la promoters , a coding sequence of gus ( | 3 - glucuronidase ) gene was fused to their downstre am , and the chimeric genes were cloned into pbin ! 9 - based plant expression vector
为了检测得到的启动子驱动效率及诱导活性，将所得到的启动子、定点突变启动子和插入花药盒的启动子与gus基因连接，构建了6个植物表达载体，同时分别构建包含ipl barnase 、 ipml barnase 、 ipmal barnase嵌合基因的植物表达载体。 - Histochemical assays in transgenic tobacco carrying b - glucuronidase ( gus ) gene fused to dgp1 showed that gus activity was found to be highly inducible by drought treatment and specifically restricted to guard cells . no gus activity was detected in roots , stems or flowers after treatment . further quantitative analysis showed that gus activity in the epidermal strips was apparently induced by dehydration and increased dramatically with the prolongation of treatment time
转基因烟草的组织化学定位表明， dgp1驱动的gus基因在受到干旱诱导的情况下，在保卫细胞中特异性表达，而在未经干旱处理植株的保卫细胞和干旱处理的根、茎和花中均不表达；对转基因烟草gus活性的定量分析表明， gus活性明显地受干旱诱导，并且随着处理时间的延长而增强，其中干旱诱导8hr后gus的活性是诱导前的179倍。
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