sequence analysis 中文意思是什麼

sequence analysis 解釋
序列分析
  • sequence : n 1 繼續；接續；連續。2 順序；程序；次第；關系；關聯。3 後果；結果；接著發生的事；後事；後文。4 ...
  • analysis : n. （pl. -ses ）1. 分解，分析；【數學】解析。2. 梗概，要略。3. 〈美國〉用精神分析法治療（＝ psychoanalysis）。
  1. The sequence analysis revealed that the as1 gene encodes a myb protein, which is a candidate transcription factor. in as1 and as2 mutants, the polarity formation in leaves is defective. cell differentiation along abaxial - adaxial, proximal - distal and media - lateral axes all shows an insufficient fashion

    通過掃描電鏡、干涉相差顯微鏡、組織切片、過量表達等手段研究了as1和as2的功能，包括觀察觀察突變體的組織、細胞結構及早期發育狀況，同時採用gus表達、 rt - pcr 、原位雜交、 northern等手段分析基因的表達情況。
  2. Polymorphism and sequence analysis of the exon 2 of bola - drb3 in cattle

    3基因第2外顯子多態性及其序列分析
  3. Authority and sequence - analysis on modern sequence change of village clansmen

    鄉村宗族秩序的現代化嬗變透析
  4. A small cryptical plasmid pefr was isolated from enterococcus faecium strain df101. the complete sequence analysis of the plasmid show that it consists of 3176 bps, which contains four putative orfs. orf1 encodes a putative protein and is highly similar to repa which functions in replication

    從屎腸球菌df101菌株中分離到隱秘的小質粒pefr ，全序列分析顯示質粒pefr由3176bp組成，編碼四個推定的orf ， orf1編碼的一個推定的蛋白和復制有關的repa有很高的相似性。
  5. Protein sequence analysis for cytochrome b5 family

    5家族蛋白序列分析
  6. Dna sequence analysis indicated that tn5gusa5 is prone to insert into low gc content regions ; guanine is a preferential base at the first place and cytosine at the last site of target sequence

    在質粒上tn5gusa5也傾向于插入低gc含量區；堿基g和c分別在靶序列的首位和末尾出現的幾率高。
  7. Cloning and sequence analysis of the cabps gene from echinococcus granulosus

    鈣結合蛋白基因的克隆和序列分析
  8. In this paper, first strand cdna of 3abc gene was synthesized using template rna extracted from cells infected with fmdv. the complete 3abc gene about isoobp was amplified by pcr and ligated into pgem - t easy vector. after transforming e. coli dh5 a, ampicillin resistant colonies were isolated and plasmid dna was prepared and analyzed by restriction analysis and pcr. presence of the full length 3abc gene was verified by nucleotide sequence analysis and the plasmid containing the expected sequence was named as pgem - 3abc. comparing the aquired sequence of 3abc with that of reference strains, the homology is more than 99 percent. the pgem - 3abc was digested with sal i and bgl ii and ligated into xho i and bgl ii - digested expression vector ptriex - 4 neo. lt was identified by restriction analysis and pcr and sequencing that this fragment had a 17bp deletion hi the nucleotide sequence 708bp of 3abc gene, which happened to form a terminator codon behind 3ab gene, but it contained the complete open reading frame ( orf ) of 3ab gene. positive clones were selected and induced with lmmol / l isopropyl - d - galactoside ( iptg ), bacteria were detected by sds - page and western blotting after properly treated. the results showed that the 3ab gene expressed successfully in e. coli and 33. 5ku fusion protein can be recognized by the positive bovine serum of fmdv. the amount of target protein is over 26 % of the total bacteria protein by gel thin layer scanning analysis

    擴增產物連接到pgem - teasy載體中，轉化大腸桿菌dh5菌株，篩選氨芐青霉素抗性菌落，提取質粒經酶切鑒定、 pcr分析以及確證性測序證明，所克隆的1500bp左右的片段含有完整的3abc基因，與國外參考序列相比，同源性在99以上。將重組質粒pgem - 3abc和表達載體ptriex - 4neo分別用sal和bgl與xho和bgl消化后，亞克隆3abc基因至原核表達載體ptriex - 4neo中，通過酶切鑒定、 pcr擴增以及序列分析，發現克隆到ptriex - 4neo載體上的片段於3abc基因708bp處出現了17bp的缺失，碰巧在3ab基因后形成一終止密碼子，但3ab基因的閱讀框架完整，選出含有3ab基因完整閱讀框架的陽性克隆，用iptg誘導表達，收集菌液進行sds - page電泳、 westernblotting分析，結果表明， 3ab基因在大腸桿菌中成功表達，其表達產物為分子量33 . 5ku的融合蛋白，並能被口蹄疫病毒陽性血清識別。經薄層掃描分析，表達量占總蛋白量的26以上。
  9. Isolation and sequence analysis of a - gliadin homologous gene from wheat

    醇溶蛋白基因同源序列的分離與序列分析
  10. Hemagglutinins inhibition ( hi ) testes showed that there were obvious variations among the isolates from different geographical areas. this result explained why the protection rates of current vaccine were different around the country. dna sequence analysis of h9 hemagglutinin genes showed that these viruses were closely related and possibly came from one source

    且在同一地域內，不同的異變體之間的差異較小，隨著時間的推移，其變異並不明顯；但在不同的區域內分離的毒株之間變異較為突出，這表明中國大陸h9n2亞型禽流感病毒不同分離株抗原性是與地域的改變而發生較為明顯的變異。
  11. Based on the structure and function analysis of hirudin, a potent thrombin inhibitor, and some platelet aggregation inhibitors, which contain the recognition sequence argglyasp as their functional motif, two chimeric antithrombotic molecules were designed by introducing rgd sequence to hirudin cterminus. these chimera genes were constructed by pcr and inserted into the expression vector pet21a, the constructs were confirmed by restriction enzyme digestion and dna sequence analysis. these recombinant plasmids were transformed into

    經限制酶消化和dna序列分析，證明兩種重組質粒與設計完全一致。由於rgd -水蛭素嵌合基因上游連接了金黃色葡萄球菌蛋白a spa的信號肽序列，在iptg誘導下兩種嵌合分子都獲得了分泌表達，表達產物主要集中在細胞周質空間。
  12. The sequence analysis of sox3 and sox4 hmg - box region in panthera tigris altaica

    4基因的保守區序列分析
  13. Since the important roles of eo protein in the viral infection. immunity and virus - host interaction. the homology of 21 csfv strains was investigated by sequence analysis of eo genes in this study, which will provide some evidence for epidemiological study. in addition, the eo gene of hog cholera lapinized vaccine ( hclv ) strain was expressed in the prokaryotic and eucaryotic systems, and the recombinant proteins were preliminarily analyzed by immunological method

    鑒于eo蛋白在病毒感染，誘導機體免疫及與宿主細胞相互關系中的作用，本研究克隆了2株豬瘟病毒eo基因並將其與其它毒株eo基因進行了序列分析，揭示了我國豬瘟病毒流行株之間的遺傳演化關系，為豬瘟病毒的流行病學研究提供依據。
  14. Cloning and sequence analysis of bos taurus hepatitis c virus core - binding protein 6 homologue gene

    牛丙型肝炎病毒核心蛋白結合蛋白6同源基因的克隆化研究
  15. Cloning and sequence analysis of apetala1 homologous gene in longan

    啟動子的克隆分析及表達載體的構建
  16. Molecular cloning and sequence analysis of lycopene - cyclase gene fragment from loquat

    基因的克隆及序列分析
  17. Cloning and sequence analysis of apetala1 homologous gene from cultivated and wild loquat

    盒基因的克隆和表達研究
  18. The sequence analysis indicated that eight of the nine analogues contained the conserved motifs of nbs - lrr of disease resistant genes, such as p - loop ( kinase la ), kinase 2, kinase 3a and trans - membrane domain. the sequence of amino acid of clone cr271 was highly homologic ( 61 % identify and 76 % similarity ) to blight resistance gene xal of rice to xanthomonas oryzae pv

    然後進行了序列的測定，通過全序列分析，結果表明：所獲得的8個抗病基因同源序列均含有nbs - lrr類抗病基因的保守序列，如p - loop （ kinase1a ） 、 kinase2 、 kinase3a以及跨膜結構域等。
  19. Cloning and sequence analysis of chi gene fragment from saussurea medusa maxim

    與以公布的chi序列orf完全一致。
  20. The phylogenetic relationship of cordyceps based on the its sequence analysis of rdna showed all of the species in this experiment have been divided into two groups by molecular systematic classification, group one including the species with perithecia wholly immersed, and group two including those with perithecia not or half immersed. it means the position of perithecia in the stroma is very important characteristic

    在埋生類群中，子囊殼斜埋生的種，即屬于新蟲草亞屬的沫蟬蟲草和雙頭蟲草，以及蟲草亞屬的下垂蟲草都被歸到一個類群之中，垂直埋生的類型被歸到另一類群中，在埋生類群中，除大團囊蟲草和c 。
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