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starting code
相关语句
  启动代码
     Realization of Starting Code Based on the ARM 32 Bit Embedded Application System
     基于ARM核的嵌入式应用系统中的启动代码的编程
短句来源
     The starting code is a piece of assemble code for application software of the 32 Bit ARM core Embedded System, which maps the C-based application code from FLASH to SDRAM, thus improving the system's speed.
     启动代码是针对基于32位ARM核的嵌入式系统的应用软件所编写的一段汇编程序,通过它将C语言编写的应用程序从FLASH存储器映射到SDRAM存储器,提高了系统的运行速度。
短句来源
     The starting code also realizes initialization of stack, of interruption and of outside devices, greatly improving the efficiency of software's development and performance.
     启动代码实现了堆栈初始化、中断初始化、外围初始化等操作,大大提高了系统的开发效率及软件性能。
短句来源
     This paper introduces the realization steps of the starting code based on the ARM 32 Bit Embedded Application System with a specific example given. It also presents code debugging and realization.
     本文详细介绍了对基于ARM核的32 位嵌入式应用系统中启动代码的编程步骤,给出了一个具体的应用实例,并结合此例对代码的编译及调试过程进行了阐述。
短句来源
  “starting code”译为未确定词的双语例句
     After that, the process of porting Linux to the FFT-RM9200 is discussed, including building the cross complier, writing the starting code, modifying and configuring of the kernel and realizing the root system.
     之后本文详细介绍了系统实现的必要工作,包括交叉编译环境的建立、启动程序的实现、内核的裁剪与移植以及根文件系统的实现。
短句来源
     After that, the process of porting Linux to the S3C44B0 is discussed, including building the cross complier, writing the starting code, modifying and configuring of the kernel and realizing the root system.
     之后本文详细介绍了系统实现的必要工作,包括交叉编译环境的建立、启动程序的实现、内核的裁剪与移植以及根文件系统的实现。
短句来源
     We synthesized antisense, sense andmismatch Oh gode oxynuc leot ide s (ODNs ) accordingto starting code AUG and four codes downtream ofthe second exon of C-myc mRNA,and modified thesynthesised ODNs by thiophosphorylation.
     针对C-mycmRNA第二外显子起站码AUG及下游4个密码子设计合成了反斗、正义及错配寡核苷酸(ODNS),并对合成的ODNs进行了疏代磷酸化修饰。
短句来源
  相似匹配句对
     Starting with B.B.O.
     本文从B.B.O.
短句来源
     asynchronous starting;
     异步起动;
短句来源
     Huffman Code
     Huffman编码的一种实现方法
短句来源
     Code Green
     绿色标准
短句来源
     Effect of Predigest Treatment on Starting Height of Lock in Range in Current Code
     现行规范对“锁住区”起点高度简化处理的影响
短句来源
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  starting code
At this point, DINK is ready to accept user commands such as downloading and starting code or assembling user programs.
      
An ideal converter presents a transfer function as being the straight line from the starting code to the ending code.
      


The I 3 and K 3 plasmids from MDV strain GA genomic Bam HI library were digested with double enzyme so that a 2.8 kb Sal Ⅰ Bam HI fragment and a 1.1 kb Bam HI Eco RI fragment were obtained. A recombinant plasmid containing the gB gene of MDV was constructed by orientation cloning the two fragments into vector pUR222. In order to manipulate gene easily and expresstion effectively, a pair of primers with enzyme sites were designed. Partial gene of MDV gB was amplified by PCR, then inserted into dephosphorized...

The I 3 and K 3 plasmids from MDV strain GA genomic Bam HI library were digested with double enzyme so that a 2.8 kb Sal Ⅰ Bam HI fragment and a 1.1 kb Bam HI Eco RI fragment were obtained. A recombinant plasmid containing the gB gene of MDV was constructed by orientation cloning the two fragments into vector pUR222. In order to manipulate gene easily and expresstion effectively, a pair of primers with enzyme sites were designed. Partial gene of MDV gB was amplified by PCR, then inserted into dephosphorized vector plasmid in correct direction. As a result, a Eco RI site increased in front of start code of MDV gB gene. The gB gene excised with Eco RI from recombinant plasmid was cloned into deophosphorized BmNPV transfer vector pBF14. DNA sequencing demonstrated that the cloned gene and reading frame were all right. After co transfection of Bm cells with wild type BmNPV and recombinant transfer vector, recombinant viruses were selected by using combination of limit dilution dot hybridization and plaque techniques. Fluorescent antibody test indicated that on the surface of the plasma membrane and plasma of Bm cells infected with recombinant virus, a strong fluorescent reaction occurred.

将马立克氏病病毒(MDV)GA株基因文库中的BamHII3和K3克隆质粒分别用双酶切消化,获得2.8kb的BamHI-SalⅠ片段和1.1kb的BamHI-EcoRI片段,然后将这2个片段定向克隆于载体pUR222中,构建了含MDV糖蛋白B(gB)基因的重组质粒。为了基因操作方便和高效表达,设计了1对带有酶切位点的引物,用PCR扩增了MDVgB基因部分片段,并按正确方向插入去磷酸化的载体质粒中,得到起始密码子前带有EcoRI酶切位点的MDVgB基因克隆,再将该基因插入去磷酸化的家蚕核型多角体病毒(BmNPV)转移载体pBF14中,DNA序列分析确证了克隆基因及阅读柜架的正确性。以重组转移载体与野生型BmNPV共转染家蚕细胞,用有限稀释法点杂交结合空斑技术纯化重组病毒。用荧光抗体试验检查重组病毒感染的家蚕细胞,可见感染细胞的胞浆及胞膜出现强荧光反应

About 61 bp noncoding sequences before the start code ATG at the 5′end of two fusion gene HBsAg/LHRH (avian and mammalian type) were deleted by PCR. Then they were directly inserted into the pBluescript 11 KS + vector DNA. The DNA sequening revealed that the modification and cloning were correct. The modified fusion gene were cloned into pET 15b vector and induced with IPTG, they all expressed fusion protein HBsAg/LHRH which is about 25 000 in molecular weight by SDSPAGE. Fusion protein HBsAg/LHRH...

About 61 bp noncoding sequences before the start code ATG at the 5′end of two fusion gene HBsAg/LHRH (avian and mammalian type) were deleted by PCR. Then they were directly inserted into the pBluescript 11 KS + vector DNA. The DNA sequening revealed that the modification and cloning were correct. The modified fusion gene were cloned into pET 15b vector and induced with IPTG, they all expressed fusion protein HBsAg/LHRH which is about 25 000 in molecular weight by SDSPAGE. Fusion protein HBsAg/LHRH were identified with antiLHRH antibody by westernblot and identified with HBsAg·Ab by ELISA. Thinlayer chromatographtscanning indicated that the expressing quantity of fusion protein HBsAg/LHRH is about 10% of total cell protein.

应用聚合酶链反应(PCR)对畜型和禽型两个融合基因HBsAg/LHRH的5′端分别作了改造,切去了融合基因起始密码ATG前一段非编码序列61个碱基,将改造后的融合基因插入pBluescripe11KS+质粒中。琼脂糖凝胶电泳以及序列分析均表明改造和克隆成功。将改造后的融合基因克隆到含T7Promoter强启动子的表达载体pET15b中,经异丙基硫代半乳糖苷(IPTG)诱导,在E.coliDE3中表达,表达量占菌体总蛋白的10%,以兔抗LHRH抗体进行Western-blot检测,出现阳性反应带。用抗HBsAg抗体作ELISA检测,结果稀释1×10-6时仍为阳性反应。

We synthesized antisense, sense andmismatch Oh gode oxynuc leot ide s (ODNs ) accordingto starting code AUG and four codes downtream ofthe second exon of C-myc mRNA,and modified thesynthesised ODNs by thiophosphorylation. The inhibition of antisense ODNs (ASODN) of C-myc on thegrowth of human SMMC-7721 hepatoma cells wasobserved in culture. The results showed that: ① The ASODN had a significant inhibition of the growth ofhuman SMMC-7721 hepatoma cells,compared withsense and mismatch ODNS;② The effect...

We synthesized antisense, sense andmismatch Oh gode oxynuc leot ide s (ODNs ) accordingto starting code AUG and four codes downtream ofthe second exon of C-myc mRNA,and modified thesynthesised ODNs by thiophosphorylation. The inhibition of antisense ODNs (ASODN) of C-myc on thegrowth of human SMMC-7721 hepatoma cells wasobserved in culture. The results showed that: ① The ASODN had a significant inhibition of the growth ofhuman SMMC-7721 hepatoma cells,compared withsense and mismatch ODNS;② The effect of the inhibition increased with the increasing of the dosageof ASODN and changed with the time of ASODNI③ The measurements by Flow cytometry provedthat ASODN mainly blocked the G2 to S of the cycling of bepatoma cell. It was demonstrated that ASODN inhibited growth of human hepatoma cellswith sequence specificity and cycling specificity,andthe effect of the inhibition related to dosage and timeof ASODN.

针对C-mycmRNA第二外显子起站码AUG及下游4个密码子设计合成了反斗、正义及错配寡核苷酸(ODNS),并对合成的ODNs进行了疏代磷酸化修饰。在人肝癌细胞SMMC-7721培养体系中,对反义寡核苷酸(ASODN)抑制细胞增殖的作用进行了研究。发现①与正义和错配ODNs相比较,反义C-mycODN有明显抑制人肝癌细胞SMMC-7721生长的作用;②该生长抑制作用随ASODN剂量增加而增强,随ASODN作用时间而变化;③流式细胞计数仅测定证明反义C-mycODN主要阻断肝癌细胞增殖周期的G1到S期。结果提示:反斗C-mycODN在体外有序列特异性和细胞周期特异性抑制人肝癌细胞的生长作用,且该抑制作用与ASODN作用时间及剂量有关。

 
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