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- Serratia marcescans nuclease 粘质沙雷氏菌核酸酶
- He also named the bacterium Serratia marcescens. 他把此菌命名为粘质沙雷氏菌。
- The methods of nuclease extraction from malt root were studied in this paper. 主要研究了麦芽根中核酸酶的提取方法。
- A small number of genes in the mother's egg set outside the nuclease. 母体卵子中的少数基因游离于核酸酶外。
- Cloning and Sequence Analysis of Serratia marcescens Chitinase chiB Gene[J]. 引用该论文 叶辉;程备久;朱苏文;甘德芳;冯春.
- The paper was published because Serratia marascens infections are very rare. 该论文被发表由于沙雷氏菌属的Marascens感染是非常罕见的。
- Objective The two incisions were contrasted in the difference of phacoemulsificafion for hard nucleas cataract. 目的比较硬核白内障超声乳化术两种切口的区别。
- But "this [zinc-finger nuclease] technology is probably going to stick around," he predicts. 但是“这种‘锌指核酸酶’技术可能会停留一段时间”,他预测。
- Nuclease extraction rate increased with the increasein ion strength and reached the highestlevelatI= 0.4M. 核酸酶的提取率随着离子强度的提高而提高,并在离子强度0.4M时达到最高。
- AAC(6’)-I is common among Serratia spp. but less frequent in other Enterobacteriaceae. AAC(6’)-I多见于沙雷菌属,但在其他肠杆菌科菌中较少发现。
- Further types of bacteria that were found include Bacillus, Serratia marcesens and Enterobacter aerogenes. 其他类型的细菌,发现包括芽孢杆菌,沙雷氏菌雷氏和产气肠杆菌。
- He used a" zinc finger nuclease " Protein (zinc finger protein), stripping to T-cell surface of the CCR5 gene. 他采用一种名为“锌指核酸酶”的蛋白质(即锌指蛋白),来剥离T细胞表层的CCR5基因。
- These serratia almost have the same culture and biochemical characteristics and produce dull yellow pigment. 其培养性状及生化特性基本一致,均可产生暗黄色色素。
- Secondly, the preparing conditions of magnetic cross-linked nuclease P1 aggregations was primarily studied. 其次,对制备磁性交联酶聚集体(CLEAs)的条件进行了初步探索。
- The zinc-finger design allows us to target a single gene, while the nuclease disrupts the gene. 我们可以通过对锌指的设计来靶向单个(特定的)基因,与此同时,核酸酶的存在将破坏该基因。”
- Objective:To evaluate the efficacy of Serratia marcescens in the malignant pleural effusions. 目的:评价粘质沙雷菌菌苗(S-311抗癌菌苗)治疗恶性胸腔积液的作用和毒性。
- Perhaps this protein is a candidate for the nuclease activity required for target RNA degradation. 作为降解靶标RNA所必需具有的核酸酶活性,它是一个候选蛋白。
- Firstly, nuclease P1 was embeded in polyacrylamide gel, and couple-linked to chitosan with glutaraldehyde. 首先,分别以聚丙烯酰胺包埋、壳聚糖偶联固定核酸酶P1。
- The unspecific reaction of Serratia marcescens could be eliminated by using the plate medium which has been added of 1% sucrose. 与粘质沙雷氏菌的交叉反应改用加1%25蔗糖的分离平板也可排除。