編碼序列 的英文怎麼說

中文拼音 [biānmǎxùliè]
編碼序列 英文
code sequence
  • 編 : Ⅰ動詞1 （編織） weave; plait; braid 2 （組織; 排列） make a list; arrange in a list; organize; gr...
  • 碼 : Ⅰ名詞（表示數目的符號或用具） a sign or object indicating number; code Ⅱ量詞1 （指一件事或一類的...
  • 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...
  • 編碼 : encoded; code; coded; encrypt; codogram; coding編碼表 encode table; 編碼程序 builder; 編碼尺 code...
  1. 8 % ), which is similar to the mt protein of ostrea edulis while different from that of drosophila and mammalian ( no aromatic amino acid and histidine ). comparison of the deduced amino acid sequence of housefly mt with other species " mt showed that its identity with drosophila was highest, attain 65 % ; the different metallothioneins, within a part species of invertebrate, were 35 % - 41 % isologous ; its identi ty wi th the mt - ii of green monkey was 41 % and that with the human mt - ii was 35 %

    由擴增片段的編碼序列所推導的家蠅mt與其它生物mt比較顯示：家蠅mt氨基酸序列與果蠅（ drosophilamelanogaster ） mtn氨基酸序列的同源性最高，達到65 ；與部分無脊椎動物mt氨基酸序列的同源性在35 - 41的范圍內；與部分植物mt氨基酸序列的同源性比較結果為：同源性最高的為孢子植物墨角藻（ fucusvesiculosus ） （ 51 ） ，而最低的為種子植物鼠耳芥（ arabidopsisthalianal ） （ 35 ） ；與哺乳動物綠猴mt -的同源性達到41 ，與人類mt -的同源性為35 。
  2. The nj map and simplest principle map based on 3 ' end coding sequences are identical to the two maps based on the complete coding sequences. this shows that 3 " end coding sequences of epsp can replace the complete coding sequences to analyze the molecular evolution

    用epsps基因全長編碼區的dna序列構建的nj圖，最簡約樹與用其3 』端編碼區dna序列構建的樹形圖相同，表明完全可以用epsps基因3 』端編碼區dna序列代替基因全長編碼序列作進化分析。
  3. The sequence of quinolone resistant determing regions ( qrdr ) of gyrase subuint a of salmonella analysis indicated that the gyra gene of strain sll - 3 share 95. 8 % respectively identities with the sequence that griggs reported which showed a high homology between the strains

    對1株耐藥菌株的染色體pcr擴增產物進行了測序，與griggs等在genbank中注冊的沙門氏菌gyra基因qrdr的編碼序列進行比較，同源率為95 . 8 。
  4. The introns are cut out by processing enzymes in the nucleus and the exons(coding sequences)ligated together.

    核內的加工酶切下內含子，同時外顯子（編碼序列）連接在一起。
  5. Intron a noncoding dna sequence that occurs between coding sequences ( exons ) in many eukaryote genes

    內含子：是大多數真核生物基因中位於編碼序列（外顯子）之間的不編碼的dna序列。
  6. The statistical analyses of base elements for e. coli coding sequences

    大腸桿菌編碼序列堿基片段的統計分析
  7. The - glc squence of tea plant consists of 1475 bp, including 189bp 3 ' utr, 233bp 5 ' utr and 1050bp open reading frame. the deduced amino acids ( aa ) sequence is a 350aa - glc precursor which consists of an 82aa transit peptide and a 257aa mature protein

    結果表明，該序列的3 』 -端和5 』端的非編碼序列長度分別為189bp和233bp ，開放閱讀框為1050bp ，編碼350氨基酸，其轉運肽長度為82個氨基酸，成熟蛋白由257個氨基酸組成。
  8. Then, a piece of degenerate primer was designed according to the conserved amino acids of glycine betaine abc transporter system glycine betaine - binding protein as a reversed primer. combined with the opuaa - up, a 2. 3 kb fragment was obtained through pcr. blast result showed a fragment which contained the partial opuaa, the whole opuab and partial opuac sequences were obtained

    再次，根據甘氨酸甜菜堿atp轉運系統底物結合蛋白的氨基酸保守序列設計下游簡並引物，與atp結合蛋白的上游簡並引物組合，經pcr擴增獲得2 . 1kb的條帶，測序后通過blast比較，結果顯示獲得atp結合蛋白基因的部分序列、通透酶的全部編碼序列和部分甘氨酸甜菜堿結合蛋白基因的核苷酸序列。
  9. Or as an equivalent sequence of multiple codes

    ）表示，但也可表示為等價的多編碼序列（
  10. Cloning of e. coli favorite human interferon - encoding sequence

    干擾素基因編碼序列的克隆
  11. And writes the xml document to a file using the specified

    、 xml命名空間和編碼序列化指定的
  12. Designing primer to compose the sequence of mouse doc - 1r cdna

    設計引物經全序列測定獲得小鼠doc - 1rcdna編碼序列。
  13. Thus, the sequence of codes in a gene says a good deal about how an organism functions

    因此，基因編碼序列對生物體的運作，有很大的影響。
  14. A kind of coding sequence of pseudo - prime and its general formula is given

    摘要本文研究了一組偽素數編碼序列，給出求解該序列的通項公式。
  15. Objects with xml schema data type definitions for. net framework types that are serialized using soap encoding

    對象，該. net framework類型是用soap編碼序列化的。
  16. Frequency code is not uniformity distribution and keeps to a probability distribution function defined by the spectral characteristics of the target of interest. the phase code is equally duality pseudo - random sequence and used to reduced the sidelobes of the signal correlation function. and the mismatch - phase sequence is corresponding with the frequency sequence one by one

    而頻率編碼為不均勻分佈，由所觀測目標的頻譜信息提取出概率密度函數決定頻率編碼序列的分佈；相位編碼為二元的偽隨機序列，採取均勻的二相編碼，消減同頻脈沖帶來的過高的相關函數的旁瓣；而失配相位為與頻率編碼相一一對應于各子脈沖中。
  17. It was suggested that exogenous dna fragments ( mainly non - coding sequence ) had new mutagenetic mechanism as well as insertional mutagenesis. in t1 and t2, a number of mutants were obtained

    對這種現象的分析表明，外源全dna片段（主要是非編碼序列）對轉化受體除了插入誘變的作用外，還可能存在一種新的誘變機制。
  18. The work of this dissertation is focused on research of some key technics in signal design and processing of mcpc signal. the main content of the dissertation is summarized as follows : it gives a detailed description of the form of the mcpc waveform and its mathematical model, and analyses the formation and properties of phase coded sequence. it discusses the effect of signal parameters on autocorrelation, power spectra and ambiguity function in forms of single pulse and pulse train and compares different kinds of single pulse signals and pulse train signals

    本文圍繞著多載波相位編碼信號在信號設計與信號處理的若干關鍵問題進行了研究，主要做了以下工作:描述了多載波相位編碼信號（ multicarrierphasecoded ，簡稱mcpc ）的信號形式，給出了其數學模型，對其中相位編碼序列的構成方式與特性進行了分析;從單脈沖和脈沖串兩種信號形式入手，對多載頻相位編碼信號的參數在自相關函數、功率譜密度和模糊方程上的影響作了詳細地討論，對不同調制方式的單脈沖和脈沖串信號進行了比較。
  19. Methods : a set of oligonucleotide primers were designed and used to amplify the vh and vl gene from anti - hbsag fab antibodies screened from phage antibody library. the products were cloned into puc19 vector and their sequences were analysed. the vh and vl gene fragments were tethered by a peptide linker and a leader sequence coding region, with the leader sequence added at 5 " terminus of each gene ( l - vh - linker - vl ) and designated as l - scfv

    方法以從噬菌體抗體庫中篩選獲得的抗hbsag的fab抗體基因為模板，分別擴增出其輕、重鏈可變區（ v _ l 、 v _ h ）基因，通過重組pcr方法將輕、重鏈可變區基因用連接肽（ gly _ 4ser ） _ 3的編碼序列連接，並引入前導肽編碼序列，構建具有l - v _ h - linker - v _ l結構的單鏈抗體基因。
  20. Conversely, the relation between the amount of nonprotein - coding dna sequences and organism complexity is more consistent

    相對的，非蛋白質編碼序列和生物復雜程度的關聯，反而相當一致。
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