sequence construct 中文意思是什麼
sequence construct
解釋
順序構造-
Distinct layers of ejected material on the volcanoes' slopes are allowing geologists to construct the chronological sequence of their formation.
噴發出來的物質層次分明地留在火山斜坡上，使地質學家們可以確定它們形成的年代順序。 -
Deduced amino acid sequence of s1, s2, pvin were also highly homologous each other ( 98 %, 99 % in each case ). the stilbene synthase genes were excised from the plasmids by bamh i and sac i digestion and intergrated into a binary vector, pbi121 and pev2, from which the p - glucuronidase ( gus ) gene sequence had been removed by the same digestion to prepare a 35s promoter - stilbene synthase 2 - nopaline synthase polyadenylation site construct and a tfp2 promoter - stilbene synthase 1 - nopaline synthase polyadenylation site construct. the recombinant plasmids were called pbs2, pev2s 1. respectively
用bamhi和saci同時酶切ps2 （ s2表示來自雷司令的芪合酶基因） 、 ps1 （ s1表示來自粉紅玫瑰的芪合酶基因）以及pbi121 、 pev2 ，使得s2 、 s1分別插入替代pbi121 、 pev2中的gus基因，構建成植物表達載體pbs2 、 pev2s1 ， pbs2中含camv35s組成型啟動子，使s2基因能在番茄植株的各個部位表達； pev2s1則含有果實特異性啟動子tfp2 ，使s1基因只在番茄果實中表達。 -
In summary, we constructed and characterized a bac library of silky, a unique chinese native breed of chicken. the library has high genome coverage ( 13 - fold ), chimerism ( 6 % ) and overlapped bacs, which made it a valuable resource to complete chicken physical map, study functional genes and construct bac contigs. we analyzed the whole genomic sequence and snps of tyrp1 and found that silky tyrp1 is different with other breeds both in microsatellite and transcription regulation site
中國農業人學博卜學位論文摘要本研究構建了中國特有雞種絲羽鳥骨雞基因組bac文庫並進行了文庫質量鑒定，它所具有的13倍高基因組覆蓋率、 6 %的嵌合率和部分重疊的克隆使其成為完善雞的基因組圖譜、研究基因功能和構建bac重疊群的優質資源。 -
By blasting the homologous sequences in genbank databases, the sequence of grass carp gh cdna from pituitary is 98 % homologous compared with the previously cloned gh cdna of grass carp. the cgh cdna fragment was inserted into pgex - 4t - l to construct the expression plasmid. the recombinant plasmid was digested by bamh i and ecor i to identify whether the cgh cdna fragment was inserted into the plasmid, the pgcgh was transformed into e. coli bl21 competent cells
將得到的序列在genbank和embl數據庫中進行了同源比較，結果顯示：本研究克隆到的草魚gh基因與genbank中登記的x60474草魚gh基因有12個堿基的差異，編碼的氨基酸有3個氨基酸殘基的差異，同源性為98 ，影響蛋白質高級結構的保守二硫鍵為2個。 -
In programming languages, a language construct within a procedure designating an end of an execution sequence in the procedure
在編程語言中，過程內標明過程內執行序列結束的語言結構。 -
Firstly, the pretreatment of character to be recognized is researched, stressed discussing the subdivisional process of character, and a kind of fast shape preserving morphological thinning algorithm is used. in the following, how to construct the structure model on the basis of characteristic point ) sub - stroke and their interrelation is discussed, and a kind of method that describe sub - stroke through the feature of the sequence of curvature is brought forward. finally, the paper adopts the recognising model of printing number that base on repository, and describes the constructing method of repository
文中首先對待識別字元的預處理進行了研究，著重探討了字元的細化過程，採用了一種基於數學形態學的保形的快速細化演算法；接著探討了如何以特徵點和子筆段及其相互關系為基礎構造結構模型，提出了一種以曲率序列性質描述子筆段的方法：最後採用了以知識庫為基礎的印刷體數字識別模型，並詳細地描述了知識庫的構造方法。 -
Objective : construct high - level expression system of echistatin in e. coli methods : obtain amino - acid sequence of echistatin from genebank database. considering the bias of usage of 61 available aminoacid codons in e. coli, design the coding sequence of echistatin, synthesize the dna sequence chemically, get single copy coding gene and repeated two copy coding gene of echistatin. insert the sequence into expression vector pbv220, and more, we construct fusion expression clone of echistatin with pcr, identify the recombinant vector by dna sequencing
目的構建蛇毒鋸鱗蝰素（ echistatin ）的原核高效表達體系方法由genebank數據庫檢索蛇毒鋸鱗蝰素（ echistatin ）的氨基酸序列，結合大腸桿菌蛋白質合成體系對氨基酸密碼子使用的偏愛性，設計了echistatin編碼基因，體外人工合成編碼基因dna片段，通過適當的限制性內切酶位點插入表達載體pbv220 ，分別構建了echistatin的單拷貝表達克隆、雙拷貝串聯表達克隆；進一步通過pcr技術構建echistatin的融合表達基因克隆。 -
The simplest way to construct milestones is to take the timing information from the work breakdown structure and sequence diagram
設置里程標最簡單的方法是從工作細分結構和任務排序表中提取時間信息。 -
Then. with the help of some good results of differential equations theory, some sufficient conditions for all solutions of the equations to be oscillatory are obtained. the way is to proof by contradiction and construct sequence
1 ）的振動性，首先，利用積分變換，給出了幾個引理，將此類差分方程轉化為相應的微分方程或微分不等式，得出了新變量的一些重要性質；然後用反證法和構造序列的方法，充分利用微分方程理論中的一些重要結論，得到此類差分方程解振動的若干充分條件 -
Gfp gene was also fused behind the signal peptide sequence to construct plasmid p3301ubisiggfp and transformed to tobacco. the results of fluorescent detection showed gfp localization in the apoplast
Elisa結果顯示，馬鈴薯蛋白酶抑制劑基因的信號肽序列使crylac基因在轉基因煙草中的表達量顯著提高。 -
In this study, we designed a pair of primers based on the sequence of the upstream and downstream of chicken il - 2 gene. about 600 bp chicken il - 2 cdna fragment was cloned from cona - stimulated chicken splenocytes by reverse transcription - polymerase chain reaction ( rt - pcr ) and was subcloned into puc18 vector. recombinant clone was demonstrated by restriction enzyme digestion and dna sequencing. next, we construct recombinant plasmid pproex ? t - il - 2. the cdna of chicken il - 2 gene was subcloned into bamh i / hind iii sites of vector. the recombinant plasmid pproex ? t - il - 2 was transformed into e. coli dh5a and the bacteria was induced with iptg. it was demonstrated by sds - page and western blot that a 18kda protein which was equal to chicken il - 2 protein in molecular weight was expressed in e. coli dh5a. the expression level was up to 30 % of the total bacterial proteins. the purified protein was used to prepare the antibody against chicken il - 2 protein
經酶切鑒定及dna序列測定，該基因為雞il - 2基因，其序列與sundick等報道的完全一致。在此基礎上，我們把雞il - 2基因亞克隆到大腸桿菌原核表達載體pproex ~ （ tm ） ht中，構建重組表達質粒並進行確證性序列測定，重組質粒測序結果表明將編碼雞il - 2成熟蛋白的基因正確地插入到原核表達載體pproex ~ （ tm ） ht的目的位點。重組質粒轉化受體菌dh5後用iptg於37進行誘導培養， sds - page和westernblot分析顯示，表達的雞il - 2融合蛋白分子量約為18kda ，表達的融合蛋白經薄層掃描發現目的蛋白表達量約占菌體蛋白的30 。 -
The main task of traditional methods is to construct iterative points and that of parameter control methods is to find a sequence of parameters
傳統演算法的關鍵是構造迭代點，而參數控制演算法的關鍵是構造參數序列。 -
By intro - ducing a penalty function as the following, for every e > 0, we construct a sequence of unconstrained minimization problems to approximate the constrained minimization problem. the solutions of such a sequence of unconstrained minimization problems all exist, and they converge to the solution of the constrained minimization problem in a certain sense
這列無約束極小化問題（ p _ ）的解都是存在的，並且在某種意義下收斂至原始約束極小化問題（ p ）的解，不僅如此，它們的性能指標也收斂至原始問題（ p ）解的性能指標。 -
Because of its fully sequenced genome and the most complete, contiguous nucleotide sequence of centromeric dna in plants, arabidopsis was chose as the base to construct plant artificial chromosome. we identified two candidate yac clones, cic8h8 and cic6f6, which are both proved to have the 178 bp arabidopsis centromeric repeat sequences
我們通過pcr和序列分析，選擇了含有擬南芥著絲粒區178bp串連重復序列的yac克隆作為構建人工染色體的基礎，同時也克隆了擬南芥的端粒和ars等序列。 -
Based on traditional derivative theories of commercial banks to operate internationally, retrospect of international development of overseas banks ’ international operation, combined with international operation history and current situation of our country ’ s state - owned banks, this paper puts forward strategies for international operation, that is, conducting a perfect market access study of targeted country, advancing ladder likely in term of territory, following the prescribed order in terms of organizing means, improving in proper sequence in terms of product strategy, this paper puts forward to construct internal risk control system and strengthen home country ’ s regulation on overseas institutions, advance process of commercial banks ’ international operation
隨著我國加入wto 「后過渡期」的日益臨近，佔有我國金融絕對比重的國有商業銀行必然要面對與國際金融市場融合的新形勢，實施國際化經營。本文在闡述商業銀行跨國經營的傳統成因理論的基礎上，回顧海外銀行業國際化發展的歷史，結合我國國有商業銀行當前現狀，提出了國際化經營策略，即做好東道國市場準入研究，在地域上梯次推進，組織方式上按部就班，產品策略上循序漸進，以期解決在哪裡經 -
The respective outgroups acyrthosium pisum and lygus heperus knight are the new gene informations for the international biology gene bank. here we got the issrdna sequence data of the aphidiodea, which were firstly aligned by clustal w and then used to construct phylogenetic tree by mega 2. 1. the result of cervaphinae revealed that : ? he sequence included 797bp in length
本研究以越南、北京地區的蚜總科內代表蚜蟲為主要研究對象，在依據外部形態分類鑒定的基礎上，應用dna序列測定技術于蚜總科昆蟲系統學研究，通過pcr擴增獲得蚜蟲18srdna基因序列，應用clustalw程序進行同源對比，採用mega2 -
We construct a iterative system with known nonlinear and time - delay stimulation basing on the original system model, and prove that the solution sequence of the iterative system uniformly converge to the optimal solution of the original system
首先根據狀態變量含有時滯的非線性系統的模型構造一個含已知非線性和時滯激勵的線性迭代系統，並證明該迭代系統的解序列一致收斂于原非線性時滯系統的解。 -
Western blot analysis showed that rhpk - 5 ( recombinant human plasminogen kringle 5, rhpk - 5 ) protein was recognized by mab same as native hpk - 5. the result suggested that we obtained correct gene sequence of hpk - 5 and got the purified rhpk - 5. section ii : construction of pbv220 / hpk - 5 vector for obtaining high - level hpk - 5 expression system, the hpk - 5 gene was recombined with plasmid pbv220 to construct the vector of pbv / hpk - 5
Coli ）作為宿主，經sds - page分析，篩選表達量最高的菌株作為發酵用工程菌株；用western - blot方法鑒定hpk - 5因子的免疫學活性；用搖瓶發酵的方法，研究發酵培養基的體積（溶解氧） 、組成成份及誘導起始時間和誘導持續時間對目的蛋白表達量的影響，優化hpk - 5基因工程菌的表達條件。 -
To allow secretion of the crylac protein into the intercellular space, potato proteinase inhibitor ii ( pinll ) signal peptide sequence was n - terminally fused to the crylac coding region to construct plasmid p3301ubisigac
運用pcr技術克隆了馬鈴薯蛋白酶抑制劑基因的信號肽序列，並將其分別連到crylac 、 gfp基因的5 』端，構建植物轉化載體p3301ubisigac和p3301ubisiggfp 。 -
This thesis presents the implementation of a high - speed frequency hopping system in dds + pll structure. a dsp is used to generate quasi - stochastic sequence and control the output frequency to construct required hopping maps
用dds pll的結構來實現頻率跳變，採用dsp作為偽碼發生器，控制輸出頻率，得到相應的跳頻圖案。
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