插入區 的英文怎麼說

中文拼音 [chā]
插入區 英文
patch area
  • : 動詞1. (把細長或薄的東西放進、擠入、刺進或穿入; 插上; 插進) stick in; insert 2. (中間加進去; 加進中間去) interpose; insert
  • : Ⅰ動詞1 (進來或進去) enter 2 (參加) join; be admitted into; become a member of 3 (合乎) conf...
  • : 區名詞(姓氏) a surname
  • 插入 : insert; infix; run in; break in; patch; insertion; plug in; intercalate; intercalation; intromiss...
  1. Floral aberrance of cbf1 transgenic tobacco and analysis of its flanking sequences

    1基因煙草植株的花器官變異及其插入區側翼序列的分析
  2. The pcr product was inserted into expression plasmid pet - 32a ( + ) after restriction digest. then the recombinant plasmid was identified by endonuclease analysis, pcr ampliation and dna sequencing. the report showed that the recombinant plasmid had right open reading frame

    重組質粒經酶切鑒定, pcr鑒定和測序,結果證實豬肺炎支原體黏附因子p97基因的抗原決定簇r1定向了質粒pet - 32a ( + ) ,且閱讀框架正確。
  3. The results showed that the f fragment, 728bp in length, could be a new gene with a little homology to the genes coding for polyketide synthetase or fatty - acid synthetase and the b fragment, about 4kb in length, is inferred to have repeat sequences around tn5 insertion site, in which there is homology to the wa 314 right arm of the high - pathogeniciry island of yersinia enterocolitica. to reveal any pathogenicity of enterobacter cloacae b8 and its mutated strains b8b and b8f to animals, the experiment with mice was carried out

    結果顯示, f片段長度為728bp ,與現有生物數據庫的blast比較分析,發現該序列僅有局部短於1oobp的域與polyketide合成酶基因或與脂肪酸合成酶基因有低的同源性,推測為一新基因; b片段長約4kb ,序列拼接結果推測靠近tn5位點部位有重復序列,對b片段tn5遠端的部分序列進行blast比較,發現它與小腸結腸炎耶爾森氏菌的強毒力島有一定的同源性。
  4. 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也傾向于低gc含量;堿基g和c分別在靶序列的首位和末尾出現的幾率高。
  5. Some tendency of tn5gusa5 transposition were found that all preferred sites of tn5gusa5 in xcc 8004 genomic dna are in at - rich regions ; target sequences of tn5gusa5 have some features that the probabilities of guanine and cytosine are high respectively at the head and tail base of target sequence ; the level of gene transcription does not influence insertion density of tn5gusa5 significantly

    結果表明, tn5gusa5位點有一定的規律性: tn5gusa5在xcc8004基因組上傾向于低gc含量( 50左右的密度最高)段;位點的靶序列有一定的特異性,在靶序列的首位鳥嘌呤出現的幾率高,而在靶序列的末位胞嘧啶出現幾率高; tn5gusa5的密度與該段基因的轉錄水平無明顯關系。
  6. Culture of mg7 hybridoma cells and detection of antigen - binding affinity of mg7 mab by elisa 2. construction and identification of mg7 recombinant phage antibody library mrna was isolated from cultured mg7 hybridoma cells and converted into cdna ; the variable fragments of heavy and light chain were separately amplified and assembled into scfvs with a specially constructed dna linker by pcr. the scfvs dma was ligated into the phagmid vector pcantabse and the ligated sample was transfered into competent e. co / / tg1 to generate a bacterial form of mg7recombinant phage antibody library ; volume and recombinant ratio of the library were evaluated by means of bacterial colony counts and restriction analysis ( ecor i and hind iii )

    Mg _ 7重組噬菌體抗體庫的構建及鑒定從培養的mg _ 7雜交瘤細胞中提取並分離mrna ,反轉錄成cdna ;利用pcr分別擴增mg _ 7單抗的重鏈及輕鏈可變基因,並通過? dna連接子將二者連接起來形成mg _ 7單鏈抗體基因;將mg _ 7單鏈抗體基因pcantab5e ;將連接產物轉化感受態tg1大腸桿菌,制備細菌形式的mg _ 7重組噬菌體抗體庫;通過菌落計數和限制性酶切分析( ecor和hind )評估mg _ 7重組噬菌體抗體庫的容量和重組率。
  7. Right click in the blank area of the sql editor window where you want to insert the new sql

    在「 sql編輯器」窗口空白域中要新sql的位置右擊。
  8. Click and type is also useful for inserting other items, such as graphics and tables, in a blank area of a document

    「即點即輸」功能同樣適用於在文檔的空白圖形和表格等項目。
  9. Notice that inserting data to an xml column is no different from inserting into any clob column

    注意數據到xml列中與數據到任何clob列中沒有別。
  10. To search proteins that associate with the mouse mint protein and regulate notch signaling in nuclei, and to study the function and mechanism of mint - mediated transcription repression, yeast two - hybrid assay was used to screen proteins that interact with a fragment of mint ( f5, amino acids 2226 - 2959 ). from 4x106 yeast clones transformed with the bait plasmid and a cdna library of 9 dpc mouse embryo, fifty - one were positive for nutritional screening and p - galactosidase assay. restriction digestion identified 10 independent positive clones and these were analyzed by dna sequencing these clones represent 3 correctly fused cdna fragments, which are mint, alpha a - crystallin - binding protein i ( alphaa - crybpl ), and nuclear receptor co - repressor 1 ( n - corl ), respectively

    鑒于mwt基因編碼較長,共有10799個堿基,故此我們將mint分為六段,分別命名為fi一f6 ,本研究以其中的f5 ( 222e959 )和f6 ( 296s576 )片段為研究對象,將h者分別pgb盯7載體中,結果顯示: mintfs可與核受體輔助抑制因子1階cori ) , o晶狀體蛋白結合蛋白1hlphatcrybp及mw加互作用,而f6可與igm的重鏈恆定、泛素結合酶2l6和一個未知功能的新的蛋白基因進行結合。
  11. However, the cloned promoter had 18 substitution at 18 sites, 22 deletions at 18 sites and 3 insertion at 3 sites between sites 0 - - - 1273 bp which was reported to control temporal - spatial specific expression, and 3 substitution at 3 sites, 6 deletions at 6 sites between - 1095 bp and - 1273 bp, the key functional sequence area, in comparing with known osg6b

    但是與報道的osg6b比較,在決定時空特異性的0 - 1273bp功能域內,有18處出現18堿基替換, 18處出現22堿基缺失, 3處出現3堿基;在核心功能序列域( - 1095bp - 1273bp )內,有3處出現3堿基替換, 6處出現6堿基缺失。
  12. Inserted page breaks are marked with a specific gridline pattern for easy identification

    為便於分,的手動分頁符用特定的網格圖案標記。
  13. It was interested that there was an extra six nucleosides insertion between 1647 - 1652nt ( according to the genomic sequence of la sota strain ), and the sequence were cccccc in f48e9 strain, and tcccac in zj1 strain. in order to test if insertion of this six nucleosides is related with the virulence of nd, two primers were designed to amplify the same fragment of another ten ndv strains. the result of sequence comparison of 16 strains showed that the six nucleoside was absent in lentogenic strain. this suggested that the six nucleosides insertion might have relationship with the ndv virulence. compared with all known sequence of ndv. there was a special sequence ( 5 ' tctctctcctctctcctcc3 " ) in the genomic cdna of ndv f48e9 strain

    通過rt - pcr方法擴增獲得了另外10個背景清楚毒株的np - p基因間隔片段,將這些序列與f48e9 、 lasota 、 clone30 、 b1 、 zj1和v4的相應序列進行了比較,結果在參比的16個ndv毒株中在該段中除了有多個點突變外,個別毒株有堿基和缺失,所有以lasota株為代表的弱毒株均無6堿基的,而以f48e9株為首的強毒株均有此6堿基的,但有一個中等毒力的毒株dp沒有6堿基的,不過它的基因序列和lasota的幾乎相同,對于所克隆到的基因的代表性還有待確定。
  14. The factors affecting the spatial effects of the deep foundation pit are researched in detail with the mutual deformation analysis method. these factors include the plane dimensions of pit, ring beam, middle beams, corner braces, embedded depth and brace stiffness. the results are compared with those of two - dimensional analysis, and their differences and adaptability are clarified

    此外,本文還利用共同變形分析方法,對影響深基坑空間效應的諸多因素(包括基坑的平面尺寸效應、圈樑和腰梁效應、角撐效應、樁身深度和支撐剛度等)進行了深探討,並與目前常用的平面分析方法做了比較,指出了兩者的別及其適用性。
  15. In order to analyze the influence of airplane noise on indoor sound environment in the vicinity of beijing international airport, different of buildings, such as villages, schools, offices, commercial building are choose as monitoring objects, the characteristic of sound insulation for building around beijing international airport are monitored and analyzed

    摘要為較好的分析飛機噪聲對機場周圍居民室內聲環境的影響,研究選擇不同類型的民居房、學校(多層建築) 、基層機關辦公用房、商品房等為測試對象,對北京國際機場周邊地建築物隔聲特性(損失)進行監測與分析,結果表明:現有民居、學校、機關辦公室的隔聲特性較差,商品房的隔聲效果較好。
  16. Compared with bombyx. mori, the exon regions of alpha - amylase gene of bombyx mandarina have 13 transitions, 4 transversions and a 12bp insertions, while the intron regions have 362 transitions, 343 transversions, a 94bp insertions and a 56bp deletions. the whole alpha - amylase gene ( including the 5 ' - and 3 ' - utrs ) of bombyx mandarina has 380 transitions, 350 transversions, 113bp insertions and 57bp deletions

    野桑蠶相對於家蠶來說,在-澱粉酶基因外顯子域發生了13次轉換、 4次顛換、 12bp,在內含子域發生了362次轉換、 343次顛換、 94bp和56bp缺失,全基因(包括utr )共發生mmrttoopmi mgzx ffatt了380次轉換、 350顛換、 113hp人和57hp缺失。
  17. Graphics inserting : pasting the pattern, grading or techniques graphics in the areas be set

    圖形:設定圖形用以粘貼板圖排料圖或工藝圖形
  18. Based on a 3. 1kb pst i fragment of genomic dna of a wild s. avermitilis, a 1. 5 kb apramycin resistance fragment was inserted into sph i site of avec gene in the 3. 1 kb fragment, then a recombinant plasmid pc05 was obtained by introducing above inactivated avec fragment into mcs region of phjl401. competent cells of et12567 were transformed by recombinant plasmid pid03 and pc05 respectively

    以含有avec基因的3 . 1kb基因組dnapsti片段為基礎,將1 . 5kb的安普黴素抗性基因片段到avec基因中的sphi酶切位點,再將此失活的avec基因片段連接到具有接合轉移功能(含有orit基因)的鏈黴菌-大腸桿菌穿梭質粒phjl401的多克隆位點,由此得到重組質粒pc05 。
  19. E3d r - tree takes into account the features of moving object data and takes advantage of new cost parameters. in particular, least - cost - first search algorithm is used in the insertion algorithm to find the overall best way to insert a new record in e3d r - tree. the proof of the vidility of the algorithm is given

    在e3dr - tree中,結合移動對象數據特徵引空白域作為新的代價參數,同時,在演算法中利用最小代價優先搜索演算法確定全局最優路徑,並給出演算法正確性證明。
  20. This suggests that the integration complexity of the intervening region ( which is more complex in ( 2 ) than in ( 1 ) ) affects the complexity of crossing integrations

    這表明插入區域的整合復雜度(句2比句1復雜)影響了交叉整合的復雜度。
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