gene basis 中文意思是什麼

gene basis 解釋
基因基礎
  • gene : n. 【生物學】基因。 dominant gene顯性基因。
  • basis : n. (pl. bases )1. 基礎;基底;臺座;【地質學;地理學】坡基。2. 根據,基準。3. 主要成份;主藥。4. 【數學】基。
  1. On the basis of expound the theory of building exterior - protected construction energy consumption and the gene of influence the building energy, set up mathematics model, this article discuss the mechanism of dispelling the heat of the buildings " thermal bridge and the complication that influence it, and then synthetic analysis and calculate the influence range of building thermal bridge in exterior - protected construction column thermal bridge to the building outer wall get the conclusion that when the construction column can satisfy the building stress - area, in bulgy construction column dispel less heating than out bulgy construction column. but if the pole stuck out more than 100mm, in bulgy or out bulgy make no difference

    本文在闡述建築圍護結構耗熱原理以及影響建築能耗因子的基礎上,採用數值模擬方法,探討了建築熱橋傳熱的基本機理和影響建築熱橋傳熱的因素,進而對建築熱橋在圍護結構傳熱中的影響范圍進行了綜合分析和計算,研究了構造柱熱橋型式對建築外墻能耗的影響,得出了構造柱在滿足建築受力面積要求的情況下,內凸構造柱較外凸構造柱略能減少散熱量的結論,但是凸出過大( 100mm )無論內凸還是外凸對建築耗熱都沒有大的差別。
  2. With the successful expression of exogenous gene in plant. the advantage of plant expression system become a highlight increasingly. based on the successful expression of hbmp - 3m gene into tobacco, we maked the study o f transferring hbmp - 3m gene into tomato and hbmp - 3 gene into tobacco, in order to obtain tomato transgenic plant with hbmp - 3m gene and tobacco transgenic plant with hbmp - 3 gene, to establish basis for getting step farther of leaning the expression of hbmp - 3m gene and hbmp - 3 gene in plant, the difference between the product of hbmp - 3m gene and hbmp - 3 gene in plant and the active of expressible product

    隨著植物基因工程的迅猛發展,一些疫苗、抗體、細胞因子等異源蛋白在植物中的成功表達,植物表達系統的優點日益受到關注。本研究室在成功地將hbmp - 3成熟肽基因轉入煙草並檢測有目的蛋白表達的基礎上,進行hbmp - 3成熟肽基因轉化番茄和hbmp - 3全長基因轉化煙草的研究,以期獲得轉hbmp - 3成熟肽基因番茄和轉hbmp - 3全長基因煙草植株,為進一步研究hbmp - 3成熟肽基因和全長基因在植物體內的表達及區別奠定基礎。
  3. Molecular basis of neural - specific gene expression

    神經特異性基因表達的分子基礎
  4. In order to benefit from this new technique without any dangers, on the basis of the arguable contents, the paper put forward a series of principals with the knowledge of systematical philosophy, mathematics and ecological. agriculture : welfare principal, invariable principal of gene, non - spread principal of gene, equal principal of substance and informed perfectible principal. and then we establish a model of evaluating the social effects of gmo

    為了從這種新技術成果中獲得好處,同時又不會帶來風險,本文以爭論的內容為基礎,從轉基因作物能比傳統農作物帶來更多的社會效益的角度出發,運用系統哲學、生態農業和數學的一些知識,提出了轉基因作物研究和推廣中遵循的一系列原則:福利原則、基因穩定性原則、基因不擴散原則、實質等同性原則、以及知情選擇原則,並進而建立起評價具體的轉基因作物的社會效益的模型。
  5. On the basis of the mentioned above and the real - time pcr principal, we have designed and optimized the primers and probes, set up the real - time qualitative pcr detection system. meanwhile, using the endogenous zein - maize and lectin - soybean as interior collate gene, epsps and cryia ( b ) as target genes, set up the real - time quantitative pcr detection system

    在此基礎上,根據熒光pcr原理,設計、優化引物和熒光探針,建立了熒光pcr定性檢測方法體系,並以玉米內源基因( zein ) 、大豆內源基因( lectin )作為內標基因,以epsps和cryia ( b )作為目的基因,建立了熒光pcr定量檢測方法體系。
  6. On the basis of reviewing on the research on organization dna and applications of gene, this paper define the organization culture gene, and demostrate on its distinguishing

    在回顧企業dna研究應用的基礎上,提出並界定了企業文化基因概念,對企業文化基因識別進行了實證研究。
  7. The result shows that a vvibdv strain was obtained, the above work lay a important role for further studying on the molecular biological mechanism of antigenic drift and virulence variation of ibdv, molecular epedimiology, it also provided the basis for recombinant and gene deleted vaccine of ibdv

    本實驗可以幫助我們進一步探討ibdv抗原性漂移和毒力變化的分子生物學機制,追溯ibdv的起源,理解病毒的傳播方式。同時也為研製開發基因重組疫苗和缺失疫苗打下一定的基礎。
  8. This paper proposes that analyzing the cause and effect of defining invention and discovery can not only provide some theoretic basis for gene patents, but also enrich and perfect the foundational theory of patent law

    通過對發明與發現區分的變遷分析,我們認為,在確定基因專利性時應淡化發明與發現的區分,採用專利「三性」標準為可行之道。
  9. Vp3 gene of hl isolate of goose parvovirus derived from recombinant piasmid pproex htb - vp3 was subcloned into ecorl site of psy538, and the reporter gene lacz with promoter pll was cloned into smai site of recombinant piasmid. both vp3 gene and lacz gene were cloned into noti site of psy681, recombinan fpv transfer vector containing vp3 gene of gpv was obtained. the result is basis of construction of recombinant fpv expressing vp3 gene of gpv and gpv genetic engineering vaccine

    本研究另從含有gpvh1分離株主要結構蛋白vp3基因的重組質粒pproexhtb - vp3中切取gpvh1株vp3基因片段,將其亞克隆于psy538的ecori位點,然後將帶有痘苗病毒啟動子p11的lacz報告基因平端克隆于上述重組子的smai位點,再用noti切下同時含有vp3基因和lacz報告基因的片段,再亞克隆于psy681的noti位點,構建出含有vp3基因的重組禽痘病毒轉移載體,為構建表達vp3基因的重組禽痘病毒從而制備gpv基因工程疫苗奠定了基礎。
  10. In this paper, phylogenetic relationship of 13 species involved in 6 genera of cruciferae wer e carried out through both the clones of homologous sequences with the primers designed on the basis of conserved regions of cyp86mf gene in cytochrome p450 gene superfamily and the differential analyses of them. meanwhile, complete sequences of some genes in cytochrome p450 gene superfamily were isolated and identified by smart pcr - race strategy, and expressed in e. colt. the results were as follows : ( 1 ) isolated by pcr from 11 species of cruciferae, eleven homologous gene segments that deduced amino acids were identities of over 80 % at nucleotide sequence level and similarities of over 70 % at amino acid sequence level

    本論文以已知的細胞色素p450基因超家族成員cyp86mf基因的保守區設計引物對十字花科重要蔬菜作物的6個屬13個物種進行了同源序列的分離克隆,通過核酸序列的差異比較分析,研究了該基因在不同物種中的進化關系;同時,通過保守引物的pcr擴增和race相結合的方法對十字花科植物不同物種的細胞色素p450基因家族成員基因全長進行了分離克隆、鑒定和原核表達的研究,獲得如下研究結果: ( 1 )通過pcr從十字花科植物不同物種中擴增到11個可以推導出完整氨基酸序列的同源片段。
  11. The other classfies the calculation of mbps into the solution of inequation based on heuristic knowledge of mbps of optimal directional coordination setting in complex multiloop network and comes into equivalence of 0 - 1 integral second layout problem. on the basis of the principle of gene optimal evolution, a new approach to determine mbps is first presented and decreases the computational complexity of mbps problem

    其二,利用復雜環網方向保護最優整定配合中最小斷點集( mbps )的啟發知識,將mbps的計算歸結為解不等式,進而等價為0 ? 1整數二次規劃問題,基於基因遺傳優化計算原理,首次提出了mbps問題的基因遺傳演算法,降低了問題的計算復雜性。
  12. The writer firstly introduces the gene and gene engineering in the first part, and on the basis, the writer will analyses social or ethical problems from five fields following the operation of the gene engineering

    該文首先在第一章中對基因和基因工程作了簡單介紹並粗線條地展現了基因工程的應用領域。在此基礎上,作者從五個方面重點探討了基因工程可能會給人類帶來的社會、倫理問題。
  13. On the basis of relationship of the peak phases of the genes rhythms in different light regimes, it can be concluded that : ( 1 ) circadian expression of the clock gene varied with the appearence of light, namely the light signal, but not the light regime

    通過比較中樞與外周、全黑暗與不同光照-黑暗交替制中基因表達的峰值相位,發現: clock的晝夜節律性表達特徵與光照是否存在(即光信號)相關,但不受ld光制影響。
  14. At last, ctab - dna and sds - dna methods are used in this experiment. on the basis of optimizing experiment procedure and pcr system of the materials, the initial reversion transcription system and orthologus gene cloning technique are established

    對這3種方法比較后,確定本實驗採用ctab - dna酶消化法和sds - dna酶消化法提取白樺雄花芽組織的總rna 。
  15. All these characters were parsimoniously analyzed using paup4. 0. mitochondrial dna cytochrome b gene was adopted to discuss the sequences variations among the populations of sinibrama species and used to reconstruct the phylogenetic relationships between the genus sinibrama and some related cultrinae genera. on the basis of the analytical result, the hypothesized relationship of cultrinae by previous authors were testified

    運用線粒體dna細胞色素b基因序列對華鯿屬及其相關類群進行了系統發育重建,以探討華鯿屬魚類不同地理居群的cytb序列變異及與其他相關類群的系統發育關系,並驗證前人的一些研究結果。
  16. As well as in eukaryocyte ( hepg2 and cos - 7 ), then detect their antigenity as a basis study and explore of the choice of immunogen for preventive and therapeutic vaccines of hepatitis b. methods : the gene fragments coding 152aa ( si ) and 124aa ( s2 ) of the carboxyl terminus of hbsag were amplified by pcr from plasmid pecob6 with a pair of primers containing different endonuclease sites and were cloned into multiple cloning sites of plasmid pbks ( + )

    為乙型肝炎的預防和治療性疫苗免疫原的選擇進行初步的研究和探討。方法:本研究利用聚合酶鏈反應( pcr ) ,通過設計帶有不同酶切位點的一對引物,從質粒pecob6特異性擴增hbsag蛋白羧基末端152個氨基酸( s1 )和124個氨基酸( s2 )的基因片段,分別將二者克隆到質粒pbks ( + )的多克隆位點,篩選重組克隆。
  17. 2 ) basis of upon studies, we have also designed and sythesized the mutation ii of the cmiv that been greatly changed in the 3 " of the gene comparing with nature cmiv : the ht gf3 ( the third loop region of htgf2 specifically binding to egfr receptor ) was fused to 3 " of gene of cmiv through a flexible linker. the gene of the mutation ii of cmiv was sequenced and clonged to the vector of ptxfus to fuse to the 3 " of gene of thioredoxin

    二、在以上研究的基礎上,對cmiv抗菌肽的c端進行較大的改造,即將與腫瘤細胞過度表達的表皮生長因子受體( egfr )具有高親和性的因子多肽tgf _ 3通過疏水柔性接頭連接在抗菌肽cmiv的c端,設計完整的基因,並在大腸桿菌中利用ptxfus表達載體與硫氧還蛋白進行可溶性融合蛋白表達。
  18. In this study, a new gene c / wew, encoding cholesterol oxidase, was isolated from rhodococcus equi. 4 - 2g2 found in china, which may be useful in clinical diagnosis healthy food and pest management in agriculture. in addition, the gene has been expressed successfully, the expression product has cholesterol oxidase activity, thus this work provided theoretical basis to the development of genetic engineering of cholesterol oxidase

    本研究從我國自行分離的馬紅球菌4 ? 2g2菌株中分離到一種編碼膽固醇氧化酶的新基因choew ,它將可應用於臨床檢測、保健食品和農業抗蟲等領域;同時利用原核表達載體成功的在大腸桿菌中表達了目的基因,表現出膽固醇氧化酶酶活,為膽固醇氧化酶的基因工程利用開發作了一定的理論實驗基礎研究。
  19. Linkage analysis localizes a gene solely on the basis of its location, without regard to its biochemical function. transmission disequilibrium test ( tdt ) is one of the methods being used. the basic thought of tdt is : if the marker locus is in the neighborhood of the disease locus, then a specific marker allele associated with the disease allele will have higher frequency among diseased individuals compared to normal individuals

    該檢驗統計量的基本思想是:若標識基因座在疾病基因座附近,那麼與疾病等位基因相關聯的標識等位基因將以更高的頻率出現在生病的個體中(相對正常體) ,這個關聯的標識等位基因相對于另一個標識等位基因的不平衡傳遞表明了標識基因座和疾病基因座之間存在連鎖。
  20. This text which is on the basis of the possibility and necessity of the combination, have expounded the realization way of the combination : 1, strengthen the cultivation of enterprising spirit and construction of the corporate image, create good encouragement atmosphere for ideological and political work ; 2, use the specific intension of " people first " of corporate culture, create " harmonious atmosphere " for ideological and political work " ; 3, through merger of the corporate culture and strength of leading, widen the field of ideological and political work ; 4. utilize the materialization means of corporate culture, enrich the means and content of ideological and political work ; 5, adhere to the political direction function of ideological and political work, guarantee the socialist orientation of corporate culture construction ; 6, draw support from the profound intension of the ideological and political work, enrich and promote the content and level of corporate culture construction ; 7, use moulding, guide fu nction of the ideological and political work, pregnant with the gene of corporate culture

    本文在探討兩者契合的可能性與必要性的基礎上,對兩者契合的實現方式與途徑進行了論述,具體為: 1 、加強企業精神的培育和企業形象的建設,為思想政治工作創造良好的激勵氛圍; 2 、運用企業文化「以人為本」的特定內涵,為思想政治工作創造「人和」氛圍; 3 、藉助企業文化的整合和導向力,拓寬思想政治工作領域; 4利用企業文化的物化手段,豐富思想政治工作的手段和內容; 5 、堅持思想政治工作的政治導向功能,保證企業文化建設的社會主義方向; 6 、藉助思想政治工作的深層次內涵,豐富和提升企業文化建設的內容與層次; 7 、運用思想政治工作的塑造、引導功能,孕育企業文化基因。為實現兩者更好地契合,還需要契合機制上的保證。
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