蠶體重 的英文怎麼說

中文拼音 [cántǐzhòng]
蠶體重 英文
body weight of larva
  • 蠶 : 名詞（能吐絲作繭的昆蟲, 通常專指家蠶） silkworm
  • 體 : 體構詞成分。
  • 重 : 重Ⅰ名詞（重量; 分量） weight Ⅱ動詞（重視） lay [place put] stress on; place value upon; attach im...
  • 體重 : （body） weight
  1. The paper directed against the history and present of china silk industry, by analysing the principal contradiction of restricting industrial advance from the point of view in productive forces and production relations, and by comparing to the brasil silk inductry where its productive forces is quickly advanced, thus, author suggested that we must again construct the advantage of china silk industry, by transtforming a industrial mode, and by building a modern production and technique system in mulberry field, and by building a industry - like technique system for enterprise raise silk worm, and by firstly advancing a number new silkworm region in the cental and west district et cetea aspects

    本文針對中國蠶絲產業的歷史和現狀，從生產力和生產關系的角度分析了制約產業發展的基本矛盾，並通過和近期蠶絲生產力發展較快的巴西進行比較，提出應從產業模式改造、建立現代化桑園生產技術體系和工業化養蠶技術體系、發展一批以中西部地區為主的新蠶區等方面，重新營造中國蠶絲產業的優勢。
  2. Abstract : the paper directed against the history and present of china silk industry, by analysing the principal contradiction of restricting industrial advance from the point of view in productive forces and production relations, and by comparing to the brasil silk inductry where its productive forces is quickly advanced, thus, author suggested that we must again construct the advantage of china silk industry, by transtforming a industrial mode, and by building a modern production and technique system in mulberry field, and by building a industry - like technique system for enterprise raise silk worm, and by firstly advancing a number new silkworm region in the cental and west district et cetea aspects

    文摘:本文針對中國蠶絲產業的歷史和現狀，從生產力和生產關系的角度分析了制約產業發展的基本矛盾，並通過和近期蠶絲生產力發展較快的巴西進行比較，提出應從產業模式改造、建立現代化桑園生產技術體系和工業化養蠶技術體系、發展一批以中西部地區為主的新蠶區等方面，重新營造中國蠶絲產業的優勢。
  3. The 53kd and 37kd proteins ( named vp53 and vp37, respectively ) encoded by the 5 ' - terminal genes of rna2 of broad bean wilt virus 2 ( bbwv - 2 ) are c - co - terminally overlapping proteins results from two potential translation sites in rna2

    蠶豆萎蔫病毒2 （ bbwv - 2 ） rna2編碼的前體蛋白能切割加工產生一種c ?端重疊的功能未知的蛋白，分子量分別為53kd和37kd ，因而將其命名為vp53 vp37 。
  4. The pbacph - egf plasmid dna was used to co - transfect bmn cell with the modified bombyx mori baculovirus bm - bacpak dna, which was first linearized by aocl. after two rounds of plaque isolation, the recombinant virus ( named bmbacph - egf ) was further verified with pcr and dot hybridization. the recombinant bmbacph - egf virus was used to infect bmn culture cells at a moi of 10

    重組轉移載體dna與經bsu36i酶切線性化的修飾型病毒bm - bacpakdna共轉染家蠶bmn細胞，兩輪空斑篩選和純化，獲得重組病毒rbmbacph - egf ，經pcr擴增、 dna點雜交等方法鑒定證實重組病毒中已正確插入ph - egf融合基因。
  5. As an insect expressing system, silkworm has long been thought highly of. however, because the relation between insects and mammals is in evolution is so distant, we do not have the exact idea if the introns of the mammalian gene can be spliced correctly in insect cells and what influence the intron imposed upon the gene expressed in the insect cells

    家蠶作為一種昆蟲表達體系受到人們的重視，但是由於昆蟲與高等哺乳動物在進化上相距較遠，高等哺乳動物基因的內含子能否在昆蟲細胞中正確剪切，內含子對此基因在昆蟲細胞中表達影響如何，目前有許多的爭論。
  6. No trace of any newly expressed protein band was noticed in supernant as well as in the cells by sds - page, except the verification of the substitution of beta - galactosidase gene ( the lose of galactosidase protein band ), which is a selective marker of the wild - type virus. elisa test results suggested the expression of egf in cells, but not in culture supernant. the quantitative calculation suggested the expressed egf was about 6 - 7 u g ( as egf standard ) per flask ( 2 > < 106 cells ) in the cellular extract

    將重組病毒rbmbacph - egf以10moi感染bmn細胞， 72小時后收集培養細胞和上清；培養上清和經超聲波處理的細胞樣品elisa檢測發現胞內樣品中存在能與egf抗體免疫反應的產物，粗略估計表達量約6 7 g 2 10 ~ 6個細胞（相當于egf標準品） ；重組病毒rbmbacph - egf穿刺接種5齡家蠶幼蟲，每隔24h收集蠶血淋巴，經elisa檢測發現第4天表達量最高，根據egf標準曲線計算蠶血淋巴的表達量約32 g ml ； elisa定性實驗還發現正常蠶血也存在與egf抗體間交叉反應的物質。
  7. The chemical components of silkworm pupa crust were analyzed, and its microstructure was characterized by using scanning electron microscope. the existing realtion of among chitin 、 protein and inorganic salt in silkworm pupa crust has been observed. the results show that the major protion of silkworm pupa chitin is in pupa crust, and it accounts for about one forth of crust weight, the out surface of pupa crust is regular polygon net vein characteristics. chitin takes honeycomb shape in chitin - protein complex and conjugated with protein. the inner space of chitin - protein complex net was filled with inorganic salts. thus the theory basis was provided for working out the process route of isolation pupa chitin

    對桑蠶蛹皮的成分、結構進行了化學及掃描電鏡分析，確定其含有的主要成分及含甲殼素的數量，並對其中的甲殼素、蛋白質和無機鹽三者之間的存在方式進行了觀察.研究結果表明，蛹體中的甲殼素與灰分主要含在蛹皮中，甲殼素占整個蛹體成分的2 . 71 % ，占蛹皮重量的25 . 5 % ，蛹皮外表面呈規整的多邊形網狀結構，蛹皮中蛋白質與蜂窩狀的甲殼素相結合，呈層狀分佈，顆粒狀的無機鹽填充在甲殼素/蛋白質復合物構成的蜂窩狀的空隙中.這為制定提取蛹甲殼素的工藝路線提供了理論依據
  8. This dissertaion, on the basis of the other studies, on the one hand, researched and analysed the chromosomes and mitoses of the cell line - bmn, which is widely used in the silkworm baculovirus expression system as an engineering cell. on the other hand, the dissertation attempted to explore establishment of the new silkworm embryoni cell line by primary culture

    同時，家蠶體外細胞培養研究的進行，不僅可以為家蠶細胞生物學的基礎理論研究提供良好的研究系統，而且在家蠶資源的開發與利用方面也具有重大的意義。本研究在借鑒前人研究的基礎上，一方面對現在廣泛應用於家蠶桿狀病毒表達系統的工程細胞? bmn細胞的染色體和有絲分裂進行了研究與分析。
  9. Then bm cell line was co - transfected with parental bm - npv dna and the transfer plasmid pvl - nk, the recombinant virus was then obtained subsequently with routine procedure. nattokinase was expressed in silkworm larva by injection with the recombinant virus

    將nk基因克隆至轉移載體pvl - 1393中後用常規方法獲得重組病毒，感染家蠶后納豆激酶獲得正確表達。
  10. Fusion gene by pcr was inserted into bombyx mori baculovirus transfer vector pbacpak. 8 and contransfected with lineared dna of bm - bacpak6 virus into bmn cells. the homologous recombination occurred inside the cells, and the recombinant virus bacpak - 6aa - hgm - csf was expressed, as identified by pcr and southern hybridization. the bmn cells and the fifth instars were infected by the recombinant virus bacpak - 6aa - hgm - csf

    本研究首先通過pcr將家蠶桿狀病毒多角體蛋白起始密碼子后的18個堿基引入到hgm - csf基因的5 』端之前，然後將融合基因重組與家蠶桿狀病毒轉移載體pbacpak8中，獲得重組轉移載體pbacpak8 - 6aa - hgm - csf ，並與線性化bm - bacpak6dna共轉染家蠶細胞株，獲得重組病毒bacpak - 6aa - hgm - csf 。
  11. The bmn cells and fifth instars were infected by the recombinant virus bacpak - angiostatin. the bioactivity of the protein product was determined by human umbilical vein endothelial cells ( ecv304 ) growth assay in vitro and inhibition of vascular growth assay in cam in vivo. angiostatin showed significantly inhibitory effect on endothelial cells

    重組病毒以moi = 10感染家蠶細胞（ 2 10 ~ 6個細胞/ 5ml ）和家蠶5齡幼蟲，表達產物用體外培養的人臍靜脈血管內皮細胞（ ecv304 ）及體內雞胚尿囊膜（ cam ）新生血管實驗檢測其抑制活性： （一）血管抑素可明顯抑制體外培養的內皮細胞增殖。
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