consensus sequence 中文意思是什麼
consensus sequence
解釋
共有序列-
At first, 1. 67 u g per well mcab all was coated on three wells of a plate, and then 1. 5 x 1011 phage virion was diluted and added, after incubating with the target, wash away unbound phage by tbst ( 0. 1 % tween - 20 ), the bound phage was eluted with ph 2. 2 tris - gly buffer and amplified, the specially bound phage was enriched by taking through addition binding / amplification cycles. ln the following cycles, the stringency of panning can be increased by raising the concentration of tbst or decreasing that of mcab all, collecting and titering the washing phage of last time and output phage in each round, the selective ratio and the false positive rate of each round were worked out, the gradually increasing of selective ratio and decreasing of positive rate shows that the panning was effective. after 4 rounds of panning, 11 phage clones were selected after competitive - ellsa, the dna samples of 8 positive clones and 1 negative clone were sequenced and all the foreign peptides inserted was also deduced, a clear consensus binding sequence emerged
在本實驗中，利用隨機12肽庫對抗豬瘟病毒（ classicalswinefeverviruscsfv ）糖蛋白me2的單抗a11進行表位篩選，經過四輪篩選以後，隨機挑取11個克隆作競爭- elisa檢測，結果表明，所挑11個克隆中，有9個克隆能對me2蛋白和a11反應產生抑制作用，抑制率最高可達64 ； dna測序以後經過dnastar軟體分析，發現它們的核心序列為anwralsl ，該核心序列與豬瘟病毒e2蛋白的28 - 35位氨基酸ttwkeysh具有同源性；夾心- elisa檢測和western - blotting試驗均證明所挑陽性克隆能被a11所識別；人工合成含核心序列的多肽經間接elisa試驗證實，也能被a11識別。 -
Based on cdna sequences of ( 3 - carotene ketolase ( cr / ff ) and p - carotene hydroxylase ( c / - fz ), a 1. 6 kb crtw genomic sequence with six introns, and a 3kb crtz genomic sequence with five introns were clone, respectively. all the exon - intron junctions conform closely to gu - ag consensus splicing rule
本論文工作成功地克隆兩個關鍵酶基因的基因組序列，發現crtw和crtz分別包括6個和5個內含子序列，所有這11個內含子的剪切位點都符合gu - ag規律。 -
But polyadenylation in bacteria needs no specific consensus sequence or there is no such sequence signals found. the sites of polyadenylation of bacterial mrna are diverse, including the 3 ' ends of primary transcripts, the sites of endonucleolytic processing in the 3 ' untranslatd and intercistronic regions, and sites within the coding regions of mrna degradation products
細菌mrna多聚腺苷酸化的位點多種多樣，包括初級轉錄產物的3 』末端， 3 』端非翻譯區和順反子間區的內切酶加工位點及mrna降解產物的編碼區內，其腺苷酸化相對無特異性、無選擇性。 -
In order to use the responding ability to the inducers of pr - la promoter, two fragments, ip1 ( 900 bp ) and ips ( 603 bp ) were cloned from tobacco genomic dna by polymerase chain reaction ( pcr ) with primers designed according to the sequence reported in genbank. sequence analysis of the amplified 900 bp fragment indicated that the cloned sequence had 99 % of homology to the known sequence. its transcription start site, tata box and consensus sequence " tgac " conserved in pr genes were identical to those of pr - la promoter
根據pr - 1a基因的報道序列，設計兩對引物，以煙草基因組為模板，通過pcr擴增得到900bp （ ipl ）和603bp （ ips ）兩個目標片段，序列測定表明克隆的啟動子與報道序列具有99的同源性，轉錄起始位點、 tatabox及保守序列tgac與報道序列均完全相同。 -
In the part i, the sequence of the cloned promoter osg6b " was first analyzed. osg6b " had a whole length of 1688 bp and 98 % homology to known sequence of promoter osg6b. its transcriptional start point, tata boxes and the consensus sequences " tgtgg " conserved usually in anther - specific promoters were identical to those of reported osg6b
第一部分：對已克隆的啟動子osg6b 』進行的序列分析表明， osg6b 』全長1688bp ，與報道的osg6b有98的同源性，兩者在轉錄起始位點、 tatabox及其它花藥特異性啟動子共有的保守序列tgtgg完全相同。 -
In this dissertation, the following experiments are conducted : firstly, cloning of hpab - gene, i ) the amino acids sequences of 23 animal - peptide antibiotics were analyzed by multiple sequences alignment method and a pair of degenerated primers were designed according to the consensus sequence derived from mature peptides of some beta peptide antibiotics
人源肽抗生素hpab -的基因克隆：對動物23種型肽抗生素的氨基酸序列進行對比，選擇部分相似性較高的序列，分析其成熟肽的結構特點，抽提型肽抗生素的一級結構特徵，並以此為基礎設計簡並引物。 -
To correlate microarray data with the promoter site consensus sequence for a specific transcription factor
找出微陣列資料與特定轉錄因子的促進子共識序列之間的相互關聯性。 -
The other 15 peptides were classified into 2 groups, each group sharing a different consensus sequence that might bind a different site of the target. one peptide of each group was chemically synthesized and added to the rdrp reaction system. we found that one peptide refrained the activity of rdrp
自2組結合膚中各選擇1個環膚分子用化學方法合成，將合成膚加入rdrp反應體系后，其中1個環膚分子對rdrp活性表現明顯的拮抗作用，加入細胞培養中可對den感染細胞產生明顯的保護作用。 -
At first, we present fault - tolerant mobile agent execution as a sequence of agreement problems ; then, we design a div consensus algorithm in order to solve the agreement problems ; at the same time, we give a pipelined mode for reliably forwarding the agent between stage s and si + i
其中，我們首先將移動agent的容錯執行問題轉換為一系列的協議協商問題；然後在consensus演算法的基礎之上通過改進給出了divconsensus演算法用以實現移動agent之間的協商策略從而最終保證移動agent執行的只一次屬性；同時我們還提出了一種用於實現移動agent在不同階段之間高效可靠傳輸的通道模式。
分享友人