識別序列 的英文怎麼說

中文拼音 [zhìbiéxùliè]
識別序列 英文
eyecatcher
  • 識 : 識Ⅰ動詞[書面語] （記） remember; commit to memory Ⅱ名詞1. [書面語] （記號） mark; sign 2. （姓氏） a surname
  • 別 : 別動詞[方言] （改變） change （sb. 's opinion）
  • 列 : Ⅰ動1 （排列） arrange; form a line; line up 2 （安排到某類事物之中） list; enter in a list Ⅱ名詞1...
  • 識別 : 1 （辯別; 辯認） discriminate; distinguish; discern; tell the difference; spot 2 [計算機] identif...
  1. Recently, ldl apheresis has been applied in clinic and achieves a satisactory effect. in this dissertation, the tripeptide, serine - aspartic - glutamic acid ( sde ), which existes in the cooh - terminal end of the seven repeats in the ligand binding domain of the ldl receptor and plays an important role in identifying ldl, was synthetized and immobilized onto the polyacrylamide ( paam ) beads as a bionic adsorbent for selective removal of ldl from plasma

    本論文以絲氨酰-天冬氨酰-谷氨酸（ sde ）負電性三肽（此三肽廣泛存在於ldl受體配體結合域7個重復序列的羧基末端，對ldl受體特異性識別ldl起著重要作用）作為配體固定到聚丙烯酰胺微球載體上製成仿生性ldl親和吸附劑，考察其對人血漿中ldl及hdl的吸附功效。
  2. Capsid proteins are involved in recognition and infection of the host and can be used to identify the virus by serological means or amino acid sequencing

    衣殼蛋白與寄主的識別和感染有關，還可以通過血清學的方法或氨基酸序列來識別病毒。
  3. 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。
  4. The characteristics of tm - 22 expression presented in transgenic tobacco : 1 ). virus specificity in either homozygote or heterozygote ; 2 ) tm - 22 gene integrated in tobacco genomic dna with single copy and in inheritance and segregation to progenies on the mendel role ; 3 ). transgenic line with tm - 22 promoter ( ptm47 ) showed infected symptoms with cell death distinguished to one with 35s promoter ( ptm49 ) after inoculation with tomv - 2a

    其次，通過氨基酸序列和結構的比較，確定tm - 2 ~ 2基因的編碼蛋白與tomv病毒在抗病反應中相互識別的特異氨基酸及其功能；然後，應用重組dna技術，互換tm - 2 ~ 2基因和tm - 2基因的對應結構域，構建嵌合基因，獲得嵌合蛋白表達的轉化體，驗證tm - 2 ~ 2編碼蛋白中變異氨基酸的作用。
  5. The holoenzyme recognizes specific nucleotide sequences on the dna duplex(promoters).

    全酶還能識別DNA雙鏈分子上的特定核苷酸序列（起動基因）。
  6. The holoenzyme recognizes specific nucleotide sequences on the dna duplex ( promoters )

    全酶還能識別dna雙鏈分子上的特定核苷酸序列（起動基因） 。
  7. Notch interaction with its ligands induces the cleavage of its intracellular domain ( ic ), and the notch ic translocates to the nucleus and binds to rbp - j, the mammalian homolog of su ( h ), to transactivate transcription of target genes such as e ( spl ) ( enhancer of split ), hesl ( hairy and enhancer of split ) and hes5 four notch receptors and their ligands are differentially and redundantly expressed in a variety of vertebrate tissues

    它通過其識別序列（ cogtgggaa ）結合於受調控基因的啟動子區，在轉錄激活因子的驅動下調節細胞分化和個體發育相關基因的表達。在沒有n 。 tch胞內段的情況下， rbpj可與包含sm盯（ silencingmediatorforretlnoldandthyroidhormonereceptor ）和組蛋白去乙酞化酶的轉錄輔助抑制復合物結合，當notch信號被激活時； rbpj可與n 。
  8. The two single - pass transmembrane proteins, delta and serrate, have been identified as notch ligands. the transcription factor suppressor of hairless [ su ( h ) ] is the major downstream effector of notch signaling pathway. rbp - j, the mammalian homolog of su ( h ), recognizes the core sequence ( c / tgtgggaa ) of dna

    Rbp - j是果蠅促神經發生基因su （ h ） （ suppressorofhairless ）在哺乳動物的同源物，它通過其識別序列（ c tgtgggaa ）結合於受調控基因的啟動子區，在轉錄激活因子的驅動下調節細胞分化和個體發育相關基因的表達。
  9. 2 the experimental principle and method of beam - foil spectroscopy are presented, and the application of the isoelectronic sequence in the analyses of spectra is described, cowan program for the theoretical calculations is introduced

    2介紹了束箔光譜學的實驗原理和方法，說明了等電子序列及其在譜線識別中的應用，介紹了用於理論計算的cowan程序。
  10. The nucleotide acids in both conserved sequences are mutative, even the length of the spacer is variable, and they both brought troubles in determining escherichia coli promoter with computer

    由於保守序列中的堿基是可變的，而且間隔堿基的長度也是可變，這給大腸桿菌啟動子的計算機識別帶來了難度。
  11. As indicated above, several m1gs that cleaved hcmv ul54 mrna segments in vitro were successfully designed and constructed. our studies demonstrates the utility of this ribozyme m1gs for antiviral application

    我們的研究成功地利用引導序列，將核酶rnasep催化亞單位m1rna構建為序列識別的核酶m1gs ，證實了核酶在抗病毒方面的應用價值。
  12. The detailed works are as follows : the finding patterns problems in the time - series data sequence are described, and a new trend logic expression method is introduced, and its algorithm and experiment result of algorithm are given ; time - scries data are disposed, and using the arctg. slope of line as the sample of pattern recognition, so ignoring the aberrance of pattern in the classified. in addition, a new time - series pattern finding algorithm based on higher - order neural network is put forward

    同時給出了本文的具體的工作，主要是：對在時序數據序列中發現模式問題進行了描述，並介紹了一種新的趨勢邏輯表示方法，給出了其演算法及演算法的實驗結果；對時序數據進行處理，提出了利用線段的斜率反正切值作為模式識別的樣本，從而在分類時忽略模式的畸變；另外，還提出了一個新的基於高階神經網路的時序模式發現演算法。
  13. The calculation results show that the method designed is quite satisfactory. the models can reproduce the annual precipitation sequence and monthly precipitation sequence. and then the regional aridity index can be estimated statistically, in addition, they can reproduce the characteristic of history precipitation series

    這兩類模型分別用於生成模擬年降雨量序列和月降雨量序列作為地區乾旱指標序列，從而對所研究地區乾旱特徵量的統計特性進行估計，並對已發生的地區乾旱的重現期進行識別。
  14. In this paper, several mathematical definitions of self - similarity are given, and some of their properties are described. the method of justifying a self - similar process and getting its autocorrelation coefficient ( or self - similar parameter ) are also discussed. achievements which are achieved by scientific research of predecessors are summarized

    本文給出了自相似的幾種常見定義，描述了該隨機過程在數學和物理上的一些特徵，並討論了如何識別一個序列是否是自相似或長相關的以及如何定量分析其相關性強弱的問題。
  15. Based on the detailed research on the sedimentary rocks of northwest ordos basin in their textures, structures, vertical sequences and logging response, six kinds of sedimentary facies can be recognized in this work, i. e., alluvial fan, stream, fan delta, braided delta, delta, lake, barrier beach and carbonate platform, respectively, and more detailed classification of sedimentary subfacies and microfacies for each sedimentary facies are also made in the work

    本文通過對鄂爾多斯盆地西北部沉積巖沉積結構、沉積構造、垂向序列及測井響應的深入研究，識別出沖積扇、河流、扇三角洲、辮狀河三角洲、曲流河三角洲、湖泊、障壁海岸及碳酸鹽臺地等8種沉積相類型。在此基礎上，對每一種沉積相又進行了詳細的沉積亞相和微相的劃分。
  16. The method of bispectrum can extract characteristic of seismic series bispectrum and detect fracture zones by decreasing dimensions

    雙譜法通過採用模式識別的方法對地震序列的雙譜提取特徵，通過降維實現裂縫發育帶的檢測。
  17. Many glycoproteins of lower and higher eucaryotes are attached to the plasma membrane by means of a glycosylphosphatidylinositol ( gpi ). gpi - anchored proteins are synthesized on membrane - bound ribosomes. upon translocation of the pro - protein across the endoplasmic reticulum membrane, gpi : protein transamidase ( gp1t ) recognize and removes the carboxy terminal gpi signal sequence and attaches a gpi molecule to the newly exposed carboxy terminal amino acid

    Gpi化前體蛋白在依附於膜的核糖體上合成，當其易位穿過內質網（ er ）膜后，被gpi ：蛋白質轉酰胺基酶（ gpit ）識別， gpit在移走其羧基端gpi信號序列的同時將gpi分子連接至新生成的氨基酸位點上。
  18. According to the theoretical parameters and analysis of clustering identification of noises, and based on the theory of spread frequency communication and bpsk, the remote reading meter system through medium - voltage power line is realized

    根據理論參數及噪聲分類識別分析，以直接序列擴頻通信為理論基礎，採用bpsk調制解調，設計了基於中壓電力線的遠程抄表系統。
  19. It provides a core data model and a very rich set of functions and primitives for flexible query

    然而，知識管理的大多數有用之處在於操縱rdf語句的抽象模型，而不是個別序列化文件。
  20. There is no characteristic in the amino acid sequence 63 - 152 and it is the piece that we want to delete to identify the function of the segment. ie180 gene mutants deleted the 64 - 151 amino acid was amplified by muti - pcr and were cloned by pmdist - vector. the clone plasmids were named pjmp1p3p2. the segment corresponding to the sequence of 1 - 1079 amino acid of the genbank sequence amplified by pcr, its clone plasmids was named pjmp1p2. the segment corresponding to the sequence of 454 - 1079 of genbank sequence amplified by pcr and its clone plasmids is named pjmp6p2 - three clone plasmids and pcdna3 were digested by restriction enzyme bamhi and hind, the gene segment of p1p2, p1p3p2, p6p2 were recycled

    本試驗應用dnamis及prosis軟體分別對genbank中登記號為no352564的ie180序列進行了蛋白質序列分析，結果表明其1 - 34段氨基酸序列具有典型helix - turn - helix特徵序列，並且富含酸性氨基酸d及e ，是典型的dna識別序列；富含絲氨酸序列的152 - 409氨基酸序列是一個與激活有關的、潛在的磷酸化位點； 454 - 696氨基酸區域是dna結合域； 64 - 151氨基酸片段沒有明顯的序列特徵；從中可看出ie180蛋白的1 - 1080氨基酸段具有典型的轉錄激活因子結構特徵。
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