植株行列 的英文怎麼說

中文拼音 [zhízhūhángliè]
植株行列 英文
plant row
  • 植 : Ⅰ動詞1. （栽種） plant; grow; cultivate 2. （樹立） establish; set up Ⅱ名詞（姓氏） a surname
  • 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）
  • 行 : 行Ⅰ名詞1 （行列） line; row 2 （排行） seniority among brothers and sisters:你行幾? 我行三。where...
  • 列 : Ⅰ動1 （排列） arrange; form a line; line up 2 （安排到某類事物之中） list; enter in a list Ⅱ名詞1...
  • 植株 : plant n concentration
  • 行列 : ranks
  1. These confirmed the successful transformation of the a78 - 3 and a78 - 4 on selection medium containing basta. microarray on membranes were fabricated from a set of 384 pinus taeda genes ( cdnas ) related to lignin synthesis, adaptation or primary metabolism for examination of gene expression in the sublines. the results showed : ( 1 ) the correlation coefficients between the transgenic sublines a78 - 3 and a78 - 4 and the untransformed control a95 : 88 : 22 were 0. 8028 - 0. 9028, while those of a78 - 5 are 0. 8897 - 0. 9302

    選擇384個與木質素生物合成及植物生理代謝和環境適應性有關的基因或cdna片段構建尼龍晶元膜，並對轉基因細胞亞系a78 - 3 、 a78 - 4和a78 - 5和對照亞系a95 ： 88 ： 22等培養再生植株進行基因表達的微陣列檢測，結果表明： （ 1 ）三個亞系與對照之間的pearson相關系數分別為0 . 8607 、 0 . 7975和0 . 9630 。
  2. Based on the sequence analysis, the temporal - spatial speciality of osg6b " was then analyzed with transgenic tobacco plants

    在序列分析的基礎上，對os96b 』在轉基因植株中的時空特異性進行了分析。
  3. The co - cultivation had been carried out for 2 ~ 3 days. after that, the transformants were obtained by transferring explants to selection medium containing 75mg / l kanamycin and rooting medium contain - - ing 75mg / l, 100mg / l kanamycin. and its rooted frequency was 82. 5 %

    為75mg幾、 100mg l的培養基上進行生根篩選，生根率為82 5 。轉入外源基因的轉化體將會在這一系列篩選過程中發芽、生根，獲得轉基因植株。
  4. In shaded environment the microenvironment, plant morphological characteristics, leaf anatomical structure and physiological metabolism, endogenesis hormone and photosynthesis of turfgrass vary significantly in order to maintain energy equilibrium and grow well

    摘要蔭蔽環境下，草坪草的微生境、植株形態特徵、葉片解剖結構以及內源激素、光合等一系列生理代謝過程都發生了顯著變化，以保證在弱光下仍能維持生長所需的能量平衡，進行正常的生命活動。
  5. The genomics dna of the transformants was extracted and assayed by pcr with nptii primer camv35 / cp primer and the results indicated that the chloroplast shsp gene has been integrated into the genomics of the tomato. then the transgenic tomato were exposed to low temperature ( in winter, on natural condition, the top temperature was 15 ? and the lowest temperature was 5 and a set of physiology parameters were measured after 6 weeks. the results were shown as follows : 1 ) effect on growth height of the transgenic tomato and the control plants after 6 weeks at low temperature showed that the transformants had been grown faster than the control. in addition, the leaves of the control plants appeared to be much reder than the transgenic tomato, and the change were obvious followed by far from the treated time at low temperature, which suggested that the constituently expression of the chloroplast shsp had some protective fountions to the tomato at low temperature

    提取轉基因番茄基因組dna ，分別以npt和35s cp引物對其進行pcr分析，結果表明葉綠體shsp基因已整合進番茄基因組中；對轉基因番茄進行低溫處理（冬季，自然條件下（無加熱的溫室） ，白天最高溫度15 ，夜間最低溫度5 ） ，生長6周后，檢測轉基因番茄的系列生理指標，主要結果如下： 1 ）生長勢：測量轉基因番茄與對照（未轉基因番茄）的株高，結果顯示轉基因植株生長明顯快于對照，且從外觀上看到對照葉片發紅程度遠大於轉基因植株，隨著低溫時間延長，對比更加明顯，說明葉綠體shsp的組成性表達在低溫下對番茄具有一定的保護作用。
  6. The method of ctab was specifically improved for the extraction of genomic dna and total rnas from brassica oleracea l. and brassica napus l. 2. arclboler gene was amplified by pcr with template genomic dna and cdna from roots, leaves, petals, stigmas and ovaries during bud stage in brassica oleracea l. ( 200110197 ) and brassica napus l. ( y578 - 2 )

    以甘藍（ 200110197 ）和油菜（ y578 - 2 ）自交不親和系的植株為材料，提取幼苗中的gdna及花蕾期的柱頭、子房、花瓣、葉片、根的mrna ，並對mrna進行反轉錄合成cdna ，然後分別以gdna與cdna為模板擴增arc1蛋白編碼序列。
  7. To explore the feasibility of ib edible vaccine, we have transformed si gene of ibv into potato and researched the immunogenicity of it ' s expression product. the findings are as follows : 1. a pair of primers for ibv si gene were designed and synthesized according to the published nucleotide sequence of ibv si gene and multiclone sites of expression vector pbi121

    為了探索ibv可食性疫苗的可行性，我們進行了轉基因馬鈴薯表達ibv免疫原基因及其表達產物免疫原性的研究，取得以下結果： 1根據周繼勇等報道的ibv - zj971毒株s1基因核苷酸序列和pbi121植物表達載體的多克隆位點，設計併合成引物，以含s1pbs質粒為模板擴增s1基因，將擴增片段定向克隆到pbi121質粒的35s啟動子下游。
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