例句與造句

1. Expression of human papillomavirus type 16 l1 structure gene in sf9 cells and its products assembling into virus - like particles
   1在昆蟲細胞中的表達及其生物學活性
2. Now , the structure gene sequence and 3 ' - end gene sequence have been logged on genbank . the accession number is ay044918
   目前，此過敏蛋白tb22kda的結構基因與3 ’端基因序列已在genbank登錄，登錄號為ay044918 。
3. The promoter and structure genes of x phage lysis genes were amplified by pcr , respectively . the plasmid mvps was constructed for integrating the vhb gene and the lysis genes into the chromosome of e . colihms174 by ligating the lysis genes to mini - tn5
   利用pcr擴增得到噬菌體裂解基因的啟動子和結構基因( srrz ) ，連接在轉座子minitn5上，構建成為質粒mvps ，用于將vhb基因和srrz基因共同插入到e . colihms174的染色體上。
4. Technical features : adopt new technology fabrics seven results , with mature ceramic production technology , powder buwen various raw materials to be transparent , according to the natural stone structure genes , generating component fabrics , rich layers . natural stone texture stronger products
   技術特點:采用全新七級布料科技成果，結合成熟的陶瓷生產工藝技術，以各種粉料布紋加以透明原料，根據(jù)天然石材的構造基因工程，生成通體布料、層次豐富、天然石材質感更強產品
5. According to the amino acid sequence resulted from our previous research about tb22kda protein and the related literatures about gene sequence of allergenic protein in common buckwheat , we designed primers and got the structure gene successfully . by 3 ' - race method combined with nested pcr , the 3 ' - end nuclear acid sequence was also obtained ; in additon , for the 5 ' - end sequence , we selected a specific conserved nuclear acid sequence as the 5 ' primer and part of structure gene sequence as the 3 " primer , and till now , partial 5 ' - end sequence has been amplified as well
   本研究根據(jù)先前分離純化所得天然tb22kda蛋白經(jīng)maldi - tof - ms (質譜法)測得的氨基酸序列和文獻報道的過敏蛋白核苷酸序列設計引物，擴增克隆了該過敏蛋白結構基因的編碼序列；根據(jù)測得的序列設計特異性引物，并利用3 ’ - race方法結合巢式pcr擴增得到基因的3 ’末端；依據(jù)同源性比較的結果選用一段保守序列為5 ’引物，并根據(jù)結構基因內部序列設計3 ’特異性引物，進一步獲得了該基因5 ’端的部分序列。
6. It's difficult to find structured gene in a sentence. 用structured gene造句挺難的
7. We paid our main attention to cloning tb22kda gene from tartary buckwheat , expressing the structure gene and getting the purified recombinant protein , and these provide foundation for father study on the relationship between structure and function of the allergenic protein tb22kda , the orientation of the corresponding epitope and the exploration of allergenic reaction mechanism
   本研究的目的在于分離克隆苦蕎中的主要過敏蛋白( tb22kda )基因，并表達純化出其結構基因編碼的蛋白。從而為進一步研究過敏蛋白tb22kda的結構與功能，尋找其中的抗原決定簇，探討過敏原與其相應抗體相互作用機理提供依據(jù)。
8. A new e . coli promoter - probe vector phn1005 was constructed by using a red - shift enhanced gfpmut3 as reporter gene and showed the following characters : 1 , bamhi at the 5 " end of gfpmut3 structure gene could be used to clone promoter - active fragment and the strength of promoter could be quantitatively assayed . 2 , a rrnbtlt2 terminator from rrna gene at the 3 " end of gfpmut3 could permit clone strong promoter . 3 , another rrnbt1t2 terminator was inserted upstream bamhi to prevent reading through of promoters from puc19
   進一步以紅移且熒光強度提高21倍的gfpmut3為報告基因，構建了大腸桿菌啟動子探針載體phn1005 ，該載體上gfpmut3結構基因5 ’端的bamhi位點可用來克隆具有啟動子活性的dna片段并定量分析插入的啟動子強度；其3 ’端含rrnat1t2終止子，可允許克隆強啟動子；在bamhi上游同樣插入rrnat1t2終止子以防止載體puc19上的啟動子的轉錄通讀； gfpmut3結構基因上游還插入一段內含子序列使正反六種讀碼框的翻譯均可被終止，可保證gfpmut3以正確的讀碼框翻譯。