coding gene造句
例句与造句
- the genetic location of grp94 is clarified, whose coding gene is on 12q24
grp94的遗传学定位清楚，编码基因位于染色体12q24 - in chapter ii, the structural characteristics of protein-coding genes are studied
论文第二章讨论了蛋白质编码区基因的结构特征。 - m . genitalium's genome is a single, circular chromosome that is 580, 076 letters long, and contains 485 protein-coding genes
尿道支原体的基因是一个单链圆形的染色体，有58万零76个字符长，包含了485个蛋白编码基因。 - protein-coding genes make up just one of those parts ? and often a small one at that, accounting for less than 2 percent of the total dna in each human cell
蛋白质编码基因，只不过是那些组成当中的极小部份罢了，?不到人类细胞全部dna的2%。 - broadly, the science of functional genomics has developed widely accepted techniques to characterize protein-coding genes, rna genes, and regulatory regions
广泛地，遗传作用的科学得到广泛地发展，形成了表现蛋白质编码因子rna因子和调整区域普遍公认的技术。 - It's difficult to find coding gene in a sentence. 用coding gene造句挺难的
- although introns constitute 95 percent or more of the average protein-coding gene in humans, most molecular biologists have considered them to be evolutionary leftovers, or junk
其实在人类的蛋白质基因中，平均95%以上的序列是插入子，大多数的分子生物学家认为它们是演化的残馀物或是垃圾。 - the start reading framae and stop codons, base composition in protein-coding genes and the codon usage of amino acids in scolopendra multilane were compared with the three other myriapods
本研究在蛋白质编码基因起始阅读框和终止密码子、蛋白质编码区的碱基组中文摘要成、氨基酸及密码子的利用等方面把少棘蜈蚣与另三种多足类进行了比较。 - as a typical protein-coding gene, the second positions were least variable, first positions were more variable, and third positions were the most variable . although codon usage is effected by a / t bias, the amino acid composition is not varied with this bias
密码子以a、t结尾频率高，第三位是g的密码子使用较少，反映出cytb基因在密码子的使用上具有偏向性，同果蝇和蜜蜂相一致。 - scolopendra multilan is a common species belonging to scolopendromorpha, chilopoda . the sequence of scolopendra multilan mtdna determined is 11700 bp in length, about 70 % of the complete sequence . the sequenced portion contains 2 rrna genes, 1 a + t-rich region, 8 protein-coding genes and 18 trna genes
本文对少棘蜈蚣的线粒体基因组进行了研究，已经测定的序列长11700bp，约为全长序列的70，包含了2个rrna基因、1个at富含区、8个蛋白基因、18个trna基因。 - objective : construct high-level expression system of echistatin in e . coli methods : obtain amino-acid sequence of echistatin from genebank database . considering the bias of usage of 61 available aminoacid codons in e . coli, design the coding sequence of echistatin, synthesize the dna sequence chemically, get single copy coding gene and repeated two copy coding gene of echistatin . insert the sequence into expression vector pbv220, and more, we construct fusion expression clone of echistatin with pcr, identify the recombinant vector by dna sequencing
目的构建蛇毒锯鳞蝰素(echistatin)的原核高效表达体系方法由genebank数据库检索蛇毒锯鳞蝰素(echistatin)的氨基酸序列，结合大肠杆菌蛋白质合成体系对氨基酸密码子使用的偏爱性，设计了echistatin编码基因，体外人工合成编码基因dna片段，通过适当的限制性内切酶位点插入表达载体pbv220，分别构建了echistatin的单拷贝表达克隆、双拷贝串联表达克隆；进一步通过pcr技术构建echistatin的融合表达基因克隆。 - objective : construct high-level expression system of echistatin in e . coli methods : obtain amino-acid sequence of echistatin from genebank database . considering the bias of usage of 61 available aminoacid codons in e . coli, design the coding sequence of echistatin, synthesize the dna sequence chemically, get single copy coding gene and repeated two copy coding gene of echistatin . insert the sequence into expression vector pbv220, and more, we construct fusion expression clone of echistatin with pcr, identify the recombinant vector by dna sequencing
目的构建蛇毒锯鳞蝰素(echistatin)的原核高效表达体系方法由genebank数据库检索蛇毒锯鳞蝰素(echistatin)的氨基酸序列，结合大肠杆菌蛋白质合成体系对氨基酸密码子使用的偏爱性，设计了echistatin编码基因，体外人工合成编码基因dna片段，通过适当的限制性内切酶位点插入表达载体pbv220，分别构建了echistatin的单拷贝表达克隆、双拷贝串联表达克隆；进一步通过pcr技术构建echistatin的融合表达基因克隆。 - results : designed and synthesized the coding gene of echistatin . and constructe its single copy expression vector, identify the vector by dna sequencing . but it could not express echistatin in e . coli . designed and synthesized the modified coding dna of echistatin, and constructe its two copy expression vector, identify the vector by dna sequencing, but it could not express echistatin in e . coli
结果设计并合成了echistatin编码基因dna序列，构建了echistatin单拷贝表达载体，经dna测序鉴定正确后，sds-page及western-blotting结果表明：echistatin在上述菌株中未获得高效表达。