coding sequence 中文意思是什麼
coding sequence
解釋
編碼序列-
On the base of researching the theory of the scheme and analyzing the signal feature, it is obtained that the existence manners and character of distance information in the differential frequency signal. at the same time, a new conclusion is gained that the technology of frequency agility can decrease the constant error of system. it is also to say that frequency agility and frequency modulation fixed - distance fuze has the similar feature to random period frequency modulation fixed - distance fuze. according to the theory of address coding in the hopping - frequency communication, the paper presents the principle of selecting the frequency agility sequence which fit to the radio fuze and constructs the frequency agility sequence family based on the rs codes
在深入研究方案原理和分析信號特徵的基礎上，獲得了該體制引信差頻信號中，距離信息的存在形式和特點，得出了頻率捷變技術的引入降低了系統定距固定誤差這一新的結論，即頻率捷變調頻定距引信在定距性能上具有類似隨機周期調頻定距的特徵。本文引入跳頻通信地址編碼理論，結合無線電引信的具體特徵，提出了適用於無線電引信的頻率捷變序列的選擇原則，並構造了基於rs碼的寬間隔頻率捷變序列族。 -
Rlean meat percentage is one of the most important economic traints in pig breeding programs. myostatin is a negative regulator of skeletal muscle growth. null or low activity of myostatin, individual muscle of mutant amimals would show a large and widespread increase in skeletal mass. myostatin null animals have significantly larger diameter or more quantity of fiber skeletal muscle. the phenotype was termed double muscling. in order to probe the relation between myostatin and high lean meat rate and plump - hipped trait, we sythesized the c ' 80 amino acids coding sequence of porcine myostatin and costructed the cloning and expressing vector of it
肌生成抑制素（ myostatin ，即mstn ）是近幾年來（ mcpherrona . c等， 1997 ）發現的骨骼肌生長的負調控因子，它主要在骨骼肌中表達。其活性的喪失，會引起動物肌肉的過度發育，肌纖維直徑變大或肌纖維數增加，表現為雙肌癥狀。肌生成抑制素研究的突破將對豬、肉雞、肉牛等畜禽生產性能的提高具有特別重要的意義。 -
Mutations in wnk4 are missense mutations in the coding sequence near the coiled - coil domains
Wnk4基因突變是位於coiled - coil區域附近一段高度保守區域的錯義突變。 -
Cloning of the complete coding sequence of mouse oxytocin receptor gene and its eukaryotic expression
小鼠催產素受體基因編碼區全長的克隆和真核表達 -
We obtained the full length gene of hbfgf coding sequence with pcr, and adjusted the g + c content according the software dnasisv2. 5, and replaced the cys78 and cys96 with serines by site - directed mutagenesis. 2. sequence result suggested one of the recombinant is correctly synthezied and cloned
用pcr方法合成了hbfgf編碼區全長，其中前20個氨基酸的g + c含量按暨南大學碩士學位論文：大腸桿菌表達重組hbfgf結構和功能優化摘要照計算機軟體計算的結果進行了調整，第78和96位上的半瞇氨酸被突變為絲氨酸。 -
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。 -
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。 -
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。 -
Every class endues a binary code, then a set of svms are used to solve the multiple binary problems. the generalization performance of ecc - svm is analyzed, which is determined by code length, hamming distance, coding sequence and margins of svms
本文提出了基於糾錯編碼的svm多類分類演算法（ ecc - svm ） ，並分析了ecc - svm的推廣能力與編碼長度、碼間漢明距離、編碼順序以及分類間隙等之間的關系，給出了這種關系的數學描述。 -
A 12 bp sequence of the 5 " end from the polyhedrin protein gene of bmnpv was ligated to the 5 ' end of hbsag ( pres2 + s ) protein coding sequence by pcr. the fusion product coding for hbv surface antigen medium sized ( hbmp ) with 4 - additional aa of bmnpv polyhedrin protein was obtained
本研究通過pcr突變的方法，在hbsag （ pres2 + s ）前s2序列的5 』端融合了bmnpv多角體蛋白基因5 』端的12個堿基，獲得了融合乙肝表面抗原中蛋白基因（ hbmp ） 。 -
Results : a fragment of 896bp was got by rt - pcr, which contains the coding sequence of sh2 a gene
結果rt pcr擴增得到sh基因編碼序列， genbank登錄號為ay190323 ；連接到pcdna3 -
Fasl - ecd coding sequence is subcloned into pet - lla expressing vector, recombinant expression vector are named as pet - fasl - ecd. this plasmid is introduced into e. coli bl21. after induction with 1mmol / l iptg, the protein expression is analyzed and confirmed by coomassie - stained sds - page
用pcr和酶切鑒定的方法篩選出陽性重組子，將陽性重組子以ilnlnol幾iptg進行誘導表達，以sds一page分析fasl胞外區的表達。 -
The result accords to the classical analysis and the 3 ' - end coding sequence is a good model of molecular evolution and is suit to be used to establish the evolution relation map between family and genus in plants
此結果與植物經典分類相一致，說明epsps基因3 』端編碼區序列是一個很好的分子進化模型，適合於構建高等植物科之間、屬之間的進化關系圖。 -
Methods ; rt - pcr method was used to amplify the coding sequence of sh2a gene. eukaryotic recombined expression vector, pcdnas. 1 - sh2a was constructed and then transfected bel7402 cell and cos
細胞激酶活性測定相關試劑二、實驗方法通過rt pcr方法擴增shzacdna編碼序列，構建真核重組表達載體pcdna3 -
Ba - dfe mature peptide - coding sequence was cloned to the restriction site ncol and ndei of the expression vector pet - 15b, respectively, and highly expressed in e. coli bl21 ( de3 ) by the form of non - fusion and his - badfe fusion protein
Lmmol liptg誘導時，融合表達時產生分子量約為30kd 、帶有his標簽的ba dfe融合蛋白，非融合表達時則產生分子量為28kd的ba dfe 。 -
2. firstly, the vector pcambia2301g with two gus reporter genes was constructed. then one gus was substituted with the coding sequence of dsg 10 obtained by pcr, and pcambia2301g - dsg10 was constructed. finally the pcambla2301g - dsg10 was introduced into agrobacterium tumefaciens using the freeze - thaw method 3
2 、首先構建了中間載pcambia2301g ，再用它和dsg10構建了可在植物中高效表達dsg10的載體pcambia2301g - dsg10 ，並將該質粒導入根癌農桿菌（ agrobacteriumtumefaciens ） eha105中。 -
Methods : the mouse pem gene ( mpem ) cdna coding sequence was cloned into prokaryotic gst fusion protein expression plasmid pgex - 4t - 3. the recombinant plasmid was transformed to e. coli bl21 and the gst / mpem fusion protein was induced to express with iptg. the fusion protein was purified by affinity chromatography
方法： pcr擴增小鼠pemcdna編碼序列，將它克隆到含有gst的原核表達質粒載體pgex - 4t - 3上，轉化大腸桿菌bl21 ，誘導表達gst mpem融合蛋白，通過親和層析，獲得初步純化的產物，以羥胺切割驗證其一級結構。 -
A large scale dna sequencing of the random clone in the library was performed. est of glycerol - 3 - phosphate dehydrogenase gene was gained and the full - length cdna of glycerol - 3 - phosphate dehydrogenase gene then was achieved as following described. first the 3 " coding sequence and 3 ' utr glycerol - 3 - phosphate dehydrogenase gene was sequenced according to subclonin g the pgpdh - 3 plasmid
然後在對文庫隨機克隆進行測序的同時，運用生物信息學手段尋找到3 -磷酸甘油脫氫酶基因的序列表達標簽（ est ）序列，在這個基礎上對3 -磷酸甘油脫氫酶全長基因進行了克隆。 -
Furthermore, by inserting " anther box " element to the mutated area of two site - mutation promoters, another two promoters, ipmas and ipmal, were created. in order to study the chemical - inducible capacity of wild and modified pr - la promoters, a coding sequence of gus ( | 3 - glucuronidase ) gene was fused to their downstre am, and the chimeric genes were cloned into pbin ! 9 - based plant expression vector
為了檢測得到的啟動子驅動效率及誘導活性，將所得到的啟動子、定點突變啟動子和插入花藥盒的啟動子與gus基因連接，構建了6個植物表達載體，同時分別構建包含ipl barnase 、 ipml barnase 、 ipmal barnase嵌合基因的植物表達載體。 -
A program or other coding sequence that produces a result of specified type and format ( " a macro generator " ; " a microcode generator " )
產生某種指定類型和格式的結果的程序或另一種編碼序列（如「宏生成程序」 、 「微代碼生成程序」 ） 。
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