隆基 的英文怎麼說

中文拼音 [lōngjī]
隆基 英文
longyi
  • 隆 : 隆Ⅰ形容詞1 （盛大） grand2 （興盛） prosperous; flourishing; thriving 3 （深厚; 程度深） deep; in...
  1. Cloning and sequencing of acc oxidase gene from sugarcane

    氧化酶基因片段的克隆與序列分析
  2. Cloning and expression of a new acyl - homoserine lactone hydrolase gene

    一種新的乙酰高絲氨酸內酯水解酶基因的克隆和表達
  3. Methods and applications of inserting a stop codon into a cloned gene with pcr

    在已克隆基因末端添加終止密碼的方法與應用
  4. Using pij903 bearing tsr gene as a vector, the two furthermost fragments of the cluster, 4. okb and 1. 5kb in size respectively, were inserted into it

    Scp2 *的應用有兩個主要的限制，一是必須有被克隆基因簇的完整而詳細的遺傳學信息，二是要求它在被克隆基因簇的來源菌株中不能復制。
  5. Genet features and ramet population features in the rhizomatous grass species psammochloa villosa

    根莖禾草沙鞭的克隆基株及分株種群特徵
  6. The shareholder includes shenyang longji real estate agency chairman guo man uk, alliance net president left puts down shenyang household management then

    股東包括沈陽隆基房地產公司董事長郭滿英，沈陽家政聯盟網總裁左繼平。
  7. On role humanization of li long - ji in quot; chang sheng dian quot

    中李隆基形象的人性化
  8. Then, the plasmid was transformed into jm109. the full length pstvd cdna recombinant plasmid was further identified by restriction mapping analysis and the nucleotide sequence of cdna cloned in pmd 18 - t vector was analyzed with ab1 377 dna sequence. test showed that the cdna of this chinese pstvd isolate was the same as pstvd - kf - 6 mild " type " isolate which originated from naturally infected potatoes in field of cornell university potato breeding program

    利用rt - pgr技術，設計一對引物，對田間採集的經鑒定含pstvd的陽性樣品進行全序列擴增，並將所得產物純化回收，連接到pmd18t - vector中，並轉化至大腸桿菌jm109中，挑選白斑進行雙酶切（ saci / ecorv ）鑒定證明插入片段為359bp大小，進行序列測定，所得克隆基因為pstvd全序列負鏈，大小為359bp 。
  9. Luo longji and nationalism

    羅隆基與國家主義
  10. Shaher took her form and manipulated rictor so shaher could find the location of the sacred spear, longicolnis

    賈哈爾藉助她的形貌迷惑了雷克托爾，通過這個途徑獲悉了聖槍隆基努斯確切的所在。
  11. Longji company is dedicated to research and development of the horticultural suppliers for a long time, specializing in producing pack containers and greenhouse related materials and equipments

    隆基公司長期致力於園藝資材的研製與開發，專業製造育苗容器及溫室配套資材。
  12. This proof following enterprise already through the authentication, and has set up a file in the dongguan 114 nets industry and commerce enterprise database, inquires the more detailed enterprise material, please dial the dongguan enterprise information desk 96060 ( artificially ) 9686810114 billion ( to be automatic ), this enterprise numbers for 43680

    茲證明東莞市隆基塑膠電子有限公司已通過認證，並已在東莞114網工商企業數據庫中備案，查詢更詳細的企業資料，請撥東莞企業查詢臺96060 （人工） 9686810114 （自動） ，該企業編號為43680 。
  13. Pcr products were inserted into pbv - 220 with double digestion of restriction enduonuclease. the expression vectors of pbv - a pbv - b and pbv - c were constructed by orientaional cloning. through sds - page, bioactivity and function analysis of expressed protein, the function of phaa, phab and phac was confirmed

    菌株的亞克隆基因組片段中，分離出phaa 、 phab和phac三個基因片段，定向克隆至原核表達載體pbv220上，構建了三個原核生物表達載體pbv - a 、 pbv - b和pbv - c ，通過對表達載體誘導表達，表達蛋白產物的sds - page分析、生物活性與功能分析，確定了基因phaa 、 phab和phac的生物學功能。
  14. The shotgun method was only used with b. subtilis hn503. the optimun conditions for total dna extraction, enzyme digest, ligation and transformation were studied the results showed that the most important factor was transformation efficiency. since the concentration of ligation products was low in common

    在已知基因序列的條件下用pcr和rt一cr克隆基因時，對pcr和rt一pcr的反應條件、產物的回收、回收產物的酶切、酶連和轉化等條件進行了一系列的比較研究。
  15. For the first time, the complete long env gene of the jaagsiekte sheep retrovirus ( jsrv ) has been colpned from provimses in china in sheep genome and sequeneed, the gene is 1836 nucleotides long. there are 12 nucleotides mutations compared with type i and type ii jsrv counterparts the sequences of the virus was 87 % to 88 % identical to the described three jsrv env sequences

    將pcr產物純化，並與puem - t載體相連，轉化大腸桿菌，經pcr ，酶切鑒定及序列測定，得知所得env片段與型jsrv同源性為88 ，與型jsrv同源性為87 ，證明所克隆基因為外源性目的基因，至此，我們在國內首次獲得了env陽性克隆。
  16. Basic geological features and future of uranium ore in the anyuan hot dome in jiangxi

    江西安遠熱隆基本地質特徵及其鈾礦遠景
  17. In order to isolate these genes, we established a set of molecular markers for the first - pass mapping of arabidopsis genes

    為了從突變體中克隆基因，我們建立了一套分子標記（共24個）用於突變基因的初定位。
  18. Mdj - 01 strain was compared with senzhang strain in biological characters and complete genome sequence. all helped to ascertain the cause for tick - borne encephalitis erupted in china northern eastern in late years, to study on the complete cdna of tbev, genome structure and function, diagnose, prevalence and therapy. the 12 subtype - special amino acids but 486 amino acids were n ' t reported, and were important to identify tbev strain isolated newly with which subtype

    本試驗對mdj - 01株和森張株進行了生物學性狀和基因組全序列的比較，這將有助於闡明近年來tbe在我國東北再次發生流行的原因，同時為tbev全長cdna克隆、基因組結構與功能、診斷、防治等研究打下基礎。
  19. Momp gene is amplified by using pcr technologyfrom dna of l2 trachoma chlamydia. the pcr products are recombined with vectors of pmd18 - t. more over, the recombinant plasmids are colonged. the dna sequence analysis shows the insert fragment is momp dna

    本實驗採用pcr技術，從l _ 2型沙眼衣原體dna中擴增出momp基因，與pmd18 - t載體重組行t a克隆，並進行dna序列分析，證明所克隆基因為mompdna序列。
  20. These strategies involved marker - assistant selection, map - based cloning, gene silencing and dna chip technology

    這些新策略的實施，將運用分子標記及其輔助育種、基因圖譜克隆、基因沉默以及基因晶元技術等dna操作技術。
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