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timing sequence相关的网络例句

查询词典 timing sequence

与 timing sequence 相关的网络例句 [注:此内容来源于网络,仅供参考]

The common denominator of both is 20. 1 applied the Fibonacci sequence to the number 20 and carried the sequence out to 26 places.

两者的共同数字是20.1应用在数目为20的斐波纳契序列上,把序列携带到26处空间。

Niu_jiantao的正确 The Fibonacci sequence 1,1,2,3,5,8,13,21……starts with two 1s,and each term afterwards is the sum of its two predecessors,which one of the ten digits is the last to appear in the units position of a number in the Fibonacci sequence?

Fibonacci数列1,1,2,3,5,8,13,21……以两个1开头,此后每一个数都是前两个数的和。那么在Fibonacci数列中,10个阿拉伯数字中的那一个是在个位数上最后出现的?

It is proved that a generalized Ishikawa type iteration sequence convergences to the unique common fixed point of its more generalized quasi-contractive mapping sequence respect to p.

证明了广义Ish ikawa型迭代序列收敛于关于p的更广义拟压缩映射序列的唯一公共不动点。

METHODS: After AIF△1-120 gene was successfully cloned, the shorter truncated human AIF gene (AIF△1-400) was constructed by deleting the Nterminal mitochondrial localization sequence, the coding sequence of flavine adenine dinucleotide binding domain and nicotinamide adenine dinucleotide binding domain of AIF protein.The truncated human AIF gene (AIF△1-400) was inserted into the pIRES2EGFP and pcDNA3 eukaryotic expression vectors, and the coexpression vectors were then transfected into HeLa cells with LipofectAMINE.

在AIF△1-120基因克隆成功的基础上进一步改造,构建截去AIF基因线粒体定位信号,FAD结合结构域和NADH结合结构域(1-400位氨基酸)编码序列的AIF△1-400基因,将其克隆入pcDNA3和pIRES2EGFP真核表达载体,用脂质体法转染HeLa细胞,通过荧光显微镜观察,MTT检测等方法检测该基因在转染细胞中的表达及其对肿瘤细胞的促凋亡活性。

METHODS: After AIF△1-120 gene was successfully cloned, the shorter truncated human AIF gene (AIF△1-400) was constructed by deleting the Nterminal mitochondrial localization sequence, the coding sequence of flavine adenine dinucleotide binding domain and nicotinamide adenine dinucleotide binding domain of AIF protein.

在AIF△1-120基因克隆成功的基础上进一步改造,构建截去AIF基因线粒体定位信号,FAD结合结构域和NADH结合结构域(1-400位氨基酸)编码序列的AIF△1-400基因,将其克隆入pcDNA3和pIRES2EGFP真核表达载体,用脂质体法转染HeLa细胞,通过荧光显微镜观察,MTT检测等方法检测该基因在转染细胞中的表达及其对肿瘤细胞的促凋亡活性。

RESULTS suc2 gene fragment of about 1.5 kb was amplified and cloned. DNA sequencing confirmed that , compared with the published sequence, the cloned suc2 gene had correct sequ ence except for one point mutation, but that did not alter the amino acid sequence o f t he encoded peptide. By transformation of yeast cells with a constructed gene dis ruption vector, four yeast clones were obtained which showed correct auxotrophy. PCR and DNA sequencing indicated that these yeast clones had the expected genot ype.

结果用 PCR从酵母基因组DNA中扩增出大小约1.5 kb的suc2基因片段,序列测定表明除585位有一点突变外,所得suc2基因与文献报道相同,构建的定位突变载体导入酵母细胞后,得到4株营养型符合的突变体,PCR表明这些突变体中均有suc2基因的同源重组,取其中1株的PCR产物进行序列测定证实了同源重组的发生。

First is the method of recognition and reconstruction of the m sequence, then how to display the frequence of the sequence is also concerned .

本文首先介绍了m序列的特性和已调伪码解调的方法。

The functionality of the random.choice function is given a sequence, return a random element of that sequence.

函数random.choice的用处就是根据指定序列,随机返回该序列中的一个元素。

The initialized sequence header may be passed to any function that takes a point sequence on input.

被初始化的头部可以传递给其他任何包含输入点序列的函数。

Study and Simulation of Real-Time Detecting Method for Fundamental Positive Sequence, Negative Sequence and Harmonic components Based on Apace Vector.

基于空间矢量的基波正序、负序分量及谐波分量的实时检测方法。

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