誘導物質 的英文怎麼說

中文拼音 [yòudǎowùzhí]
誘導物質 英文
induced substance
  • 誘 : 動詞1. （誘導） guide; lead; induce 2. （使用手段引人隨從自己的意願） lure; seduce; entice
  • 導 : 動詞1. （引導） lead; guide 2. （傳導） transmit; conduct 3. （開導） instruct; teach; give guidance to
  • 物 : 名詞1 （東西） thing; matter; object 2 （指自己以外的人或與己相對的環境） other people; the outsi...
  • 質 : Ⅰ名詞1 （性質; 本質） nature; character; essence 2 （質量） quality 3 （物質） matter; substance;...
  • 誘導 : guide; lead; induce; guidance; induction
  • 物質 : matter; substance; material
  1. Our previous studies showed existence of apoplast cam in the plant cell and cam had many extracellular functions. so it supposed cam may be one of important extracellular polypeptides and trigger the intracellular signal transduction by binding the receptor. in this study, radiolabelled ligand is used to investigate the binding characteristic of cam and a. thaliana protoplasts. and chemical crosslinking is employed to explore binding proteins in the membrane. at first, ( 35 ) ~ s - cam was produced using ( 35 ) ~ s - labeled amino acid mixture in e. coli. sds - page and autoradiograph indicated high - purified, high - specific radioactivity ( 35 ) ~ s - cam was obtained. electrophoresis of ( 35 ) ~ s - cam is the same as that of unlabeled cam with ca ~ ( 2 + ) or egta ; a quatitive of protoplasts was prepared by enzymolysis

    首先，用~ （ 35 ） s標記的氨基酸混合物喂養工程菌成功地制備了~ （ 35 ） s標記的擬南芥鈣調素（ ~ （ 35 ） s - cam ） ， ~ （ 35 ） s - cam純度高、放射活度高、 ca ~ （ 2 + ）與egta存在時的電泳行為與未標記cam相同，可作為一種高靈敏性的探針用於進行受體學分析實驗；用擬南芥種子誘導愈傷，通過酶解制備了大量原生質體。
  2. And ha molecules were synthesized in vitro utilizing excessive active udp - glca and udp - glcnac sugar nucleotide precursors in the presence of a divalent mg2 + or mn2 + ion

    經轉化大腸桿菌dh5a和iptg誘導表達，提取原生質膜在體外利用活性前驅物合成了透明質酸。以s
  3. Section two the evaluation of biocompatibility of the acellular dermal matrix by the method of cell culture. the new born rat ' s epdermic cells were cultured with the acellular dermal matrix together as experiment group, while the epdermic cell were cultured simply as control. 24 hours later, under the invert microscope, the epidermic cells anchored well and transparent flat cells were observed in both groups. 7 days later, both cultured cells were taked out and fixed in 95 % ethanol, stained with hematoxylin and were observed under light microscope. many cleaved cells were observed in both groups. during cell culture, no pathogenic microganism was observed. so we considered the acellular dermal matrix was aseptic and had good biocompatibility. section three subdermal implantation of the acellular dermal matrix. 24 rats were used in the experiments. a piece of acellular dermal matrix ( 1. 5 x 1. 5cm2 ) was implanted beneath the dorsum skin flaps of each rat, 1 week, 2 weeks, 3 weeks and 4 weeks after implantation, 6 pieces of acellular dermal matrix were harvested and the size of implanted acellular dermal matrix were measured, the sections were used for he staining and observed under light microscope. the result were as folio wing : 1 - 2 weeks after implantation, the acellular dermal matrix began to adhere to the tissue around and turned red gradually ; 3 - 4weeks after implantation, the acellular dermal matrix adhered closely to the tissue around and could be recognized easily, 1 - 3 weeks after implantation, the size of implanted acellular dermal matrix had no statistical difference ( p > 0. 05 ). 4 weeks after implantation implanted acellular dermal matrix contracted ( p < 0. 05 ). under light microscope, l - 2weeks after implantation, the fibroblast cells infiltrated the acellular dermal matrix and a small amount endothelial cells of vessel and lympho - histiocytic cells infiltrated the acellular dermal matrix. 3 - 4 weeks after implantation, infiltrating blood vessels were evident. so we think that the acellular dermal matrix had low immunological reactions and could induce the infiltration of fibroblast macrophage cell and the endothelial cells of vessel

    結果如下：皮下包埋卜周者，無細胞真皮基質漸與周圍組織粘附，顏色由蒼白轉紅；皮下包埋3周者，無細胞真皮基質與周圍組織緊密枯附，盾晰葉辯；術后卜周，包埋的基質面積變化較包埋前無統計學差異o川0引，術后4周包埋的無細胞真皮基質面積較包埋前縮小j刃刀5 ） 。光鏡下術后卜周，宿主的淋巳組織細胞、成纖維細胞浸入生長，釉附在膠原纖維上，少量血管內皮細胞浸入基質；術后34周，無細胞真皮基質內較多的血管形成，故可認為無細胞真皮基質免疫原性低，能誘導宿主的成纖維細胞、巨噬細胞浸入生長，為一種新型的真皮替代物。第四部分無細胞真皮基質與自體斷層皮片復合移棺的研究， sd大鼠10隻，在其背部卜方造成全厚皮膚缺損的創面
  4. Florigen ( flowering hormone ) a hypothetical plant hormone that has been postulated to account for the transfer of the photoperiod stimulus from the leaves to the apex where flowering is induced

    成花激素：一種假定的植物激素，該假設用來解釋來自於葉中，在莖端誘導成花的光周期刺激物質的轉運。
  5. 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。
  6. This environmentally induced division of labor benefits the whole genet greatly, and th us is another adaptive strategies of clonal plants to grow successfully in heterogeneous environments

    這種環境誘導的克隆內分工行為有利於整個基株對資源交互斑塊性環境的利用，是克隆植物對異質性環境的生態適應對策。
  7. Following the development of the study in extracellular matrix ( ecm ), people find that the ecm is composed of glucoprotein and glycosaminoglycans, and it ' s components induct the cell differentiation in tissues and organs, in turn, it can modulate the function of these

    隨著人們對生物體細胞外基質認識的深入，明確了它是由不同含量的糖蛋白以及糖胺聚糖組成的按一定比例和結構建成的復雜的有機的統一整體。它的各組成成份，分別誘導分化組織、器官內的不同細胞，通過調節各細胞的生長、分化進而調整組織、器官功能。
  8. 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。
  9. Conclusions : prokaryotic and eukaryocytic expression plasmids of the shortened hepatitis b surface antigen were successfully constracted, and the target proteins expressed by iptg induced in escherichia coli. as well as in eukaryocyte ( hepg2 and cos - 7 ), then their antigenity were detected

    結論：截短的乙型肝炎表面抗原分子的原核和真核表達』重組質粒成功被構建及分別在人腸桿菌efl得到誘導表達和存貞核細胞ifj表達，並檢測劍其表達產物的抗原特性。
  10. At the room temperature, fluorescence intensities of these chemosensors in acetonitrile without transition metal ions were found to be very weak, due to the process of the efficient intramolecular photoinduced electron transfer ( pet )

    在室溫下對其光物理性質的研究中發現，在沒有加入過渡金屬離子時，由於體系內存在有效的光誘導電子轉移過程使得熒光團的熒光被淬滅。
  11. Corticosteroids : corticosteroids most commonly have been reported to cause drug - induced myopathy

    皮質類固醇激素是目前報道較多的能引起藥物誘導性肌病的藥物。
  12. These bacteria are transmitted through the cytoplasm of eggs and have evolved various mechanisms for manipulating reproduction of their hosts, including cytoplasimic incompatibility ( ci ), parthenogenesis, feminization, male killing, fecundity or fertility modifying etc. wolbachia are common and widespread bacteria infecting 17 % insect population, 17 crustacean species, mites and many nematodes

    這些共生菌通過母系遺傳參與調控寄主的多種生殖活動，包括細胞質不親和現象、誘導孤雌生殖現象、雌性化、雄性致死以及調節寄主生殖力等。 wolbachia的分佈十分廣泛，目前已經發現在超過17的昆蟲種群以及17種甲殼綱動物、蟎蟲、線蟲體內發現了它的存在。
  13. Induction of metamorphosis of the southern bay scallop argopecten irradians concentricus larvae by chemical cues

    化學物質對墨西哥灣扇貝幼蟲變態的誘導
  14. 97 % identities in amino acids respectively. the e. coli strain dh5 transformed recombinant plasmid phn was induced with 0. 6 mmol / m iptg for n gene expression. the expressed product was identified by sds - page and westem - blot test, a fusion protein about 47ku as we expected was found

    將含有重組質粒phn的菌株dh5在37條件下培養，以濃度為0 . 6mmol / liptg誘導，重組質粒n基因phn融合蛋白獲得了表達：經sds - page ， western - blot試驗，確定其表達的融合蛋白產物大小為預期的47ku 。
  15. They contained an antisense constructed for the spruce gene encoding ccr ( cinnamoyl alcohol dehydrogenase ), an enzyme of monolignol synthesis. the antisense rna method is a technique for reducing the expression of a resident target gene. the transgenic sublines were produced by particle bombardment at the dept of forest genetics, swedish university of agricultural sciences

    本項目研究的目的就是採用瑞典農業大學構建的反義ccr基因轉導的挪威雲杉細胞愈傷組織，通過誘導產生再生植株，並檢測證實該基因是否表達及其它相關基因的表達狀況，為培育出低木質素的轉基因挪威雲杉新品種奠定物質和理論基礎。
  16. The carbofuran - degrading experiment of cds - 1 was carried out in lab scale, the results showed that the highest degrading efficiency was obtained with ph, temperature being 7. 0, 30c respectively ; the change of aeration had no influece on degrading rate ; the increasing inocula could accelerate carbofuran degrading progress ; the degrading capability of cds - 1 was n ' t inhibited by high carbofuran concentration ; the addition of low concentration of nutrients had no distinct effect on the degrading rate while high concentration had inhibiting effect the distribution of degrading enzyme was also primarily studied, the results showed that degrading - related enzyme was endocellular and degrading progress was not cometabolism

    Cds - 1的降解酶（系）是誘導酶（系） ，存在明顯的誘導期；胞內、胞外酶實驗表明呋喃丹降解酶（系）存在於細胞內。添加低濃度外源營養物質對cds - 1的降解性能無明顯影響，說明cds - 1降解呋喃丹的過程不屬于共代謝過程，可以在無外源營養物質存在的條件下降解呋喃丹。添加高濃度外源營養物質會對該菌降解性能產生抑制。
  17. 2 ) measured the survival curves for the cells overexpressing mutant alleles of gpil7p and chosed the proper cu2 + concentration in the medium for inducing

    2 ）測定過表達了突變gpi17p細胞的存活曲線，並確定了培養介質中誘導物銅離子的適宜濃度。
  18. Procaryotic expression vector recombinant was transformed into competent bl21, induced and expressed by iptg revulsant, explored the best inducing time and the best concentration of revulsant

    將原核表達載體的重組質粒轉化大腸桿菌bl21 （ de3 ） ，用iptg誘導物進行誘導表達，探索最佳誘導時間和誘導物的使用濃度。
  19. From the result of electrophoresis, it known that the different components of the enzyme system were expressed cooperatively. in order to study the essence of cellualase induction of different carbon sources, the extracellular, plasm - membrane - bound and intracellular cellulases were made to transform different soluble inducers, and the productions were analyzed by gc chromatogram. the results supported the assumption that cellobiose acted as the direct inducer or the metabolic analogue, b - gentiobiose from cellobiose acted as the true inducer through different metabolism ways in different strains

    制備細胞膜外、細胞膜、細胞內纖維素酶，用定位於這三部位的纖維素酶分別轉化底物，然後進行氣相色譜定性分析，從而探討了不同碳源之間的誘導本質，結果認為不可溶的胞外纖維素以纖維二糖為橋梁，遵循不同的代謝途徑，直接或間接地誘導了兩株不同真菌纖維素酶的合成。
  20. The novel finding that some pem capsules can introduce spontaneous deposition of various substances provides a brand - new way of encapsulation

    新近發現的聚電解質微膠囊自身所具有的誘導物質自發沉積性質為物質的包埋開創了一條嶄新的思路。
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