株基 的英文怎麼說

中文拼音 [zhūjī]
株基 英文
thiocarbonyl
  • 株 : Ⅰ名詞1. （露在地面上樹木的根和莖） root and stem of a tree above the ground 2. （植株） individual plant; plant Ⅱ量詞（棵）
  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. While the fruits ripening process was delayed in leetrl antisense fruits. epinastic of leaves in leetrl antisense plants was only occasionally observed, which was not observed in leetr2 antisense plants ; ( 5 ) when treated by exogenous ethylene ( 25ul / l ), the abscission of antisense leetr2 petiole explants was delayed. moreover, leaf epinasty failed to be induced by ethylene treatment c, which suggested that these tissues were insensitive to ethylene

    （ 5 ）植株衰老和葉片脫落延遲，花瓣脫落也明顯的延遲，在轉反義leetr1基因番茄的果實成熟特性被明顯改變，表現在乙烯釋放高峰延遲，果實顏色出現變異，以及和成熟相關的酶活性的改變，然而，轉反義leetr2基因的果實的成熟特性與對照相比無明顯差別。
  3. There will be adventitious sprouts at the base of the rose plant.

    植株的基部會長出不定芽。
  4. High frequency of bud induction was found on ms medium supplemented with 6 - ba the optimum medium for adventitious bud induction was ms + l. 0mg / 1 naa + 0. 5mg / l 6 - ba, and ms + 1. 5mg / l naa + 0. 5mg / l iaa for bud rooting

    門）誘導毛狀根體細胞胚再生植株。通過正交實驗篩選出了毛狀根體細胞胚誘導的最佳培養基為： ms 05mg lnaa 0 sing kt 30gil蔗糖。
  5. The virulent strains had a polysaccharide capsule and formed smooth colonies on agar medium.

    有毒菌株具有多糖莢膜它在瓊脂培養基上形成光滑的菌落。
  6. It was suggested that eric - pcr could substitute for rapd in research related to the genetic identification and genetic diversity in auricularia and other edible and medicinal fungi : 2 to a certain extent, genetic differences among auricularia strains tested in this study did not have necessary relativity with their geographical origins respectively ; 3 in this study, genetic diversity in a. polytricha was higher than that in a. auricula : 4 in this study, a. fuscosuccinea had a higher homology to a. auricula than to a. polytricha ; 5 morphological characteristics validated the results from eric - pcr and provided a potential explanation for the higher similarity coefficient between a. auricular and a. fuscosuccinea ; 6 southern hybridization was employed by choosing a strain from a. auricula as a probe which hybridized with a. auricula and a. fuscosuccinea except a. polytricha, further confirming the veracity of the results from eric - pcr ; 7 in this study, isozyme analysis could not cluster the 7 strains from three auricularia species to different groups efficiently ; 8 2 strains from two auricularia species revealed high conservative degree and the restriction fragment patterns by 4 kinds of restricted enzymes showed no diversity

    本研究中，木耳屬2個種的2個菌株在its區域表現出較高的保守性， 4種限制型內切酶的酶切圖譜沒有顯示出多態性；增加內切酶種類及供試菌株數量，有可能獲得具有多態性的限制性內切酶酶切圖譜； 9本實驗中， its區域的真菌特異性引物與真核生物通用引物對于擴增效果無較大差異，擴增片段長度均為650bp左右； 10根據形態學實驗、 eric - pcr實驗以及southern雜交實驗的結果分析，紫木木耳屬種質資源的遺傳鑒定和遺傳多樣性評價耳極有可能是毛木耳種的一個變種; n .本研究中所用的gutc法是一種適用於木耳屬菌株基因組洲a快速提取的方法; 12 .傳統的形態學分類法和現代的分子生物學分類法，兩者的關系是相輔相成，互為驗證
  7. Now many laboratories have used avirulent strains of s. typhimurium to deliver h. pylori antigens as a way of stimulating an immune response to those determinants

    以鼠傷寒沙門氏菌標準株基因組dna作為模板，採用pcr的方法克隆了鼠傷寒沙門氏菌asd基因，經序列分析與文獻報道一致。
  8. The genetic relationship had been evaluated by similarity cofficient obtained from these profiles

    對rapd結果進行聚類分析，構建了各供試菌株基因型的親緣關系圖。
  9. Characterization of hemagglutinin gene of influenza a virus subtype h9n

    毒株基因組特性的研究
  10. The 496 bp fragment of the orf of p22 gene and a 561 bp fragment were amplified from the genomic dna of zs strains of toxoplasma gondii. both 496 bp and 561 bp fragments were successfully cloned into the plasmid pthiohisa, b, c and pbudce 4. 1 respectively. 2

    從弓形蟲zs株基因組中擴增出p22編碼基因的一長496bp ，另一長561bp的片段，並成功構建含p22編碼基因的原核質粒重組體pthiohisa ， b ， c / p22 ，及真核重組表達質粒pbudce4 . 1 / p22 。
  11. 2. ginlfyand ginndly gene were obtained from the leaf genomic dna of the male tree of ginkgo cultivar dafushou in the mid - april through pcr

    Dafushou ）雄株基因組dna為模板，通過pcr擴增，獲得兩個銀杏雄株leafy同源基因ginlfy和ginndly基因。
  12. Genetic subtype and epidemiological feature of hiv - 1 circulating strains in fujian province

    1流行毒株基因分型與流行特徵分析
  13. Nies - 90 microcystin producing algae strain genome library construction and one isolated gene analysis

    構建用於相關基因篩選的微囊藻產毒株基因組文庫
  14. Sequence analysis on measles viruses isolated in shanghai in

    上海地區2005年麻疹流行株基因特性分析
  15. After obvious cytopathogenic effects developed, virus - contained supematants were harvested, and the progeny viruses were screened for lacz - expressing viruses by a plaque assay using x - gal. single blue plaques were picked, and a recombinant prv stably expressing lacz gene ( designated as rprv - lacz ) was obtained after ten cycles of plague purification and pcr identification. the results showed that the lacz gene expression cassette was stably expressed in the recombinant rprv - lacz derived from bartha - k61 strain

    該載體與具有高度感染性的bartha - k61株基因組dna通過脂質體加plus法共轉染vero細胞，採用甲基纖維素固定病變， x - gal染色，經過10代藍斑純化獲得了一株穩定表達lacz基因的ge tk基因缺失突變株，命名為rprv - lacz 。
  16. The two end - points were localized on a 4. 3kb bamhl - ecor1 fragment of a cosmid 16c3 and a 1. 2kb sail fragment of a cosmid 17g7 respectively. the deletion junction was localized on a 2. 8kb bamhi fragment of the zx1 chromosome

    兩個端點分別定位在野生型菌株基因組文庫粘粒16c3的4 . 3kb的bamh1 - ecor1片段上和17g7的1 . 2kb的sal片段上，缺失界點定位在zx1染色體上的一個2 . 8kbbamh片段上。
  17. These results showed that the three isolates were infectious bursal disease virus. the full - length cdna of the genomic segment a of two viruses, one virulent field strain ibdv zj2000 and one attenuated strains ibdv jd1, were amplified in a single step procedure by long - accurate reverse - transcription polymerase chain reaction ( la - pcr ), cloned into pgem - t easy vector, and sequenced

    分別以傳染性法氏囊病病毒zj2000株（野毒株）和jd1株（弱毒株）基因組dsrna為模板，採用long - accuratert - pcr （ la - pcr ）一步法擴增並克隆了兩株病毒的基因組a節段全長cdna 。
  18. Sequences flanking tn5 - 1063a can be recovered from the genome of mutant by excision, self - ligation and transfer to e. coli. the total dna of mutant was excised with ecori, which cut the genome frequently but not cut the transposon. after sequencing the self - ligated transpon, dna fragment flanking tn5 was obtained. the result showed 042bm - x1 contains a tn5 insertion in the gene smc00190, which function was unknown and was demonstrated to be related to salt tolerance by this study, and the gene was named as rst - 0x1

    通過ecori酶切突變株基因組，得到完整的tn5 （含有在大腸桿菌中起始復制的oriv ）及其側翼的序列片段，該片段自連后轉化大腸桿菌，以tn5兩端已知的序列設計引物進行測序。 blast的分析測序結果表明， 042bm - x1和042bm - x2中tn5分別定位在苜蓿中華根瘤菌1021染色體上smc02682和smc00419基因內部，本實驗證明它們和042bm耐鹽相關，命名為rst - 0x1和rst - 0x2基因。
  19. Effect of cry3a promoter on expression by using resolution vector, the cry1ac and cry1c genes with cry3a promoter or it itself promoter were introduced into b. thuringiensis crystal negative strains. the expression of these strains is quit similar, however, the expression of cry 1 ac and crylc with different promoter in same cell has no complete inhibition

    Cry3a啟動子對基因表達的影響利用解離載體將帶cry3a啟動子的crylac10和crylc基因導入蘇雲金芽胞桿菌無晶體突變株，基因的表達和殺蟲活性與帶自身啟動子的基因的表達相近。
  20. Hcmv infection can result in a wide variety of clinical manifestations, but the mechanisms remain unclear yet. host factors such as celluar or humoral immune response might play an important role. on the other hand, genetic variability among different virus strains could influence clinical manifestations of hcmv infections

    Hcmv感染可引起不同的臨床表現，其發病機制不清，可能與宿主的體液和細胞免疫狀態有關，亦可能與不同臨床分離株基因及其編碼產物的多態性有關。
分享友人
分享到 Line

分享到臉書