例句與造句

1. the genetic location of grp94 is clarified, whose coding gene is on 12q24
   grp94的遺傳學定位清楚，編碼基因位于染色體12q24
2. in chapter ii, the structural characteristics of protein-coding genes are studied
   論文第二章討論了蛋白質編碼區基因的結構特征。
3. m . genitalium's genome is a single, circular chromosome that is 580, 076 letters long, and contains 485 protein-coding genes
   尿道支原體的基因是一個單鏈圓形的染色體，有58萬零76個字符長，包含了485個蛋白編碼基因。
4. 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
   蛋白質編碼基因，只不過是那些組成當中的極小部份罷了，?不到人類細胞全部dna的2%。
5. broadly, the science of functional genomics has developed widely accepted techniques to characterize protein-coding genes, rna genes, and regulatory regions
   廣泛地，遺傳作用的科學得到廣泛地發展，形成了表現蛋白質編碼因子rna因子和調整區域普遍公認的技術。
6. It's difficult to find coding gene in a sentence. 用coding gene造句挺難的
7. 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
   其實在人類的蛋白質基因中，平均95%以上的序列是插入子，大多數的分子生物學家認為它們是演化的殘馀物或是垃圾。
8. 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
   本研究在蛋白質編碼基因起始閱讀框和終止密碼子、蛋白質編碼區的堿基組中文摘要成、氨基酸及密碼子的利用等方面把少棘蜈蚣與另三種多足類進行了比較。
9. 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
   密碼子以a、t結尾頻率高，第三位是g的密碼子使用較少，反映出cytb基因在密碼子的使用上具有偏向性，同果蠅和蜜蜂相一致。
10. 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
    本文對少棘蜈蚣的線粒體基因組進行了研究，已經測定的序列長11700bp，約為全長序列的70，包含了2個rrna基因、1個at富含區、8個蛋白基因、18個trna基因。
11. 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
    目的構建蛇毒鋸鱗蝰素(echistatin)的原核高效表達體系方法由genebank數據庫檢索蛇毒鋸鱗蝰素(echistatin)的氨基酸序列，結合大腸桿菌蛋白質合成體系對氨基酸密碼子使用的偏愛性，設計了echistatin編碼基因，體外人工合成編碼基因dna片段，通過適當的限制性內切酶位點插入表達載體pbv220，分別構建了echistatin的單拷貝表達克隆、雙拷貝串聯表達克隆；進一步通過pcr技術構建echistatin的融合表達基因克隆。
12. 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
    目的構建蛇毒鋸鱗蝰素(echistatin)的原核高效表達體系方法由genebank數據庫檢索蛇毒鋸鱗蝰素(echistatin)的氨基酸序列，結合大腸桿菌蛋白質合成體系對氨基酸密碼子使用的偏愛性，設計了echistatin編碼基因，體外人工合成編碼基因dna片段，通過適當的限制性內切酶位點插入表達載體pbv220，分別構建了echistatin的單拷貝表達克隆、雙拷貝串聯表達克隆；進一步通過pcr技術構建echistatin的融合表達基因克隆。
13. 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
    結果設計并合成了echistatin編碼基因dna序列，構建了echistatin單拷貝表達載體，經dna測序鑒定正確后，sds-page及western-blotting結果表明：echistatin在上述菌株中未獲得高效表達。