進行行列 的英文怎麼說
中文拼音 [jìnhánghángliè]
進行行列
英文
procession-
It ' s meaningful to study the function of rab proteins in ciliates and further to explicit the mechanism of vesicular trafficking. the rob gene was amplified from macronuclear dna of euplotes octocarinatus. the size of gene was 783 bp long with an orf of 624 bp encoding eorabl protein and containing three in - frame tga codes
本研究利用pcr技術從游仆蟲( euplotesoctocarinatus )大核dna中擴增出rab基因,並對該基因進行序列分析,該基因全長為783bp ,兩端為端粒序列,編碼框為624bp ,編碼207個氨基酸,開放讀框中有3個tga ,在此編碼半胱氨酸。Using enterobacter cloacae b8, the mutated strains b8b and b8f, and the recombinant clones pb and pf, we try to sequence the antagonistic - related genes of enterobacter cloacae b8 by subcloning and genome primering system. the acquired sequences were analyzed with blast program to find any homology to sequences deposited in genebank
以廣譜拮抗菌陰溝腸桿菌b8菌株和拮抗活性缺失菌株b8b 、 b8f及從b8b和b8f二菌株克隆獲得的重組質粒pb 、 pf為基礎,對陰溝腸桿菌b8菌株拮抗相關的b和f基因片段進行序列分析。The multi - projection histograms are proposed to segment the code in the line and row, and it also solves interference and conglutination problems, achieves accurate location of the number
運用多投影直方圖分割法對鋼材區的編號進行行、列分割,並解決了干擾、字元粘連等問題,實現了編號的精確定位分割。Carrying out a series of inquiring activities with mimosa pudica
利用含羞草進行系列生物探究活動To place items in an arrangement in accordance with the order of the natural numbers
按照自然數的順序將數據項進行排列。With the rapid development of the scientific technology and the acceleration of the steps of urbanization and industrialization, the environment disruption to the natural sources done by human beings gets more and more serious. since the twentieth century, the environment problems have become more and more obvious, and the environmental crimes as well as the environmental public nuisances have happened continually, all of which have greatly threatened the human lives, the security of property, and even the social and economic development
本文以犯罪學為視角,通過描述的方法對反國際環境犯罪的法律對策、社會對策的現狀進行了列舉,然後運用列舉、對比、概括等研究方法對打擊和預防國際環境犯罪的立法現狀、執法現狀和非法律層面的合作現狀進行了評析,並提出其中存在的問題和解決的建議。By transformation with the genes. plant disease biocontrol bacteria bacillus subtil is aplls and b. megaterium ap25 were isolated from wheat field soils collected from south australia and tai an. enzyme activity analysis on chitin agar and abp media showed that b. subtilis aplls secreted chitinase and b. megaterium ap25 secreted endoglucanase, respectively
測序后在genebank上進行序列比較,該基因片段同編號為2634966的枯草芽孢桿菌全序列的2599451到2812870 (功能未知)有85的同源性,但同已發表的13種幾丁質酶的基因(包括枯草芽孢桿菌幾丁質酶基因)的同源性很低,只有30 。Pcr method was used to identify candidate ms 188. sequence analysis indicated that a point mutation occurred in the second exon of the atmyb103 gene in male sterile mutant with caa ( gln ) replaced by a stop codon taa
利用pcr的方法從突變體中擴增atmyb103基因並進行序列分析,結果表明突變體中atmyb103基因第二個外顯子上發生了點突變,由原來編碼谷氨酰胺的caa密碼子突變為終止密碼子taa 。The results of sequencing showed that jl94 isolate complete gene 6 was 1356bp and had a complete open reading frame which encoded 397 amino acides
對克隆的vp6基因進行序列測定,測序結果顯示jl94vp6基因全長1356bp ,含有完整的開放閱讀框架,編碼397個氨基酸。Further analysis showed that there are regulatory elements, including tata box and caat box, etc. pc - igs fragments were cloned and sequenced from five strains of arthrospira ( a. platensis fachb341, a. platensis fachb439, a. platensis ouqds6, a. maxima ouqdsm and a. platensis fachb791 ) and two strains of spirulina ( s. subsalsa fachb351 and spirulina fachb440 ). the cloned fragment includes 494 bp of cpcb, 252 bp of cpcaand 111 bp of pc - igs sequence
在節旋藻和螺旋藻分子系統學研究中,克隆了節旋藻和螺旋藻的藻藍蛋白操縱子中的pc - igs序列並進行序列測定和分子系統學分析,結果如下:所克隆的長度為857bp的片段包含有494bp的cpcb基因, 111bp的pc - igs序列和252bp的cpca基因。The c - phycocyanin ( cpc ) operon of blue - green alga ( or cyanobacteria ) arthrospira platensis fachb341 was cloned, sequenced and characterized by using chromoseme walking method. the sequence includes cpcb gene ( 519 bp ), cpca gene ( 489 bp ), cpch gene ( 357 bp ), and upstream sequence of cpcb ( 427 bp ) and upstream sequence of cpch genes ( 184 bp ), 111 bp of phycocyanin intergenetic spacer ( pc - igs ). upstream sequence of cpcb gene was ligated into promoter - probe vector pegfp - 1 and transformed into three systems : e. coli, synechocystis pcc 6803 and a. platensis fachb341 by supersonic and electrophoresis methods
根據genbank中報道的節旋藻藻藍蛋白基因序列設計引物,首先克隆了鈍頂節旋藻( arthrospiraplatensisfachb341 )藻藍蛋白操縱子中亞基基因、亞基基因部分序列及二者之間的間隔區序列( pc - igs )並進行序列測定,然後根據此測序結果設計引物,通過染色體步移法克隆得到藻藍蛋白操縱子長度為2086bp的基因片段,其中包括藻藍蛋白亞基基因( cpcb , 519bp ) ,亞基基因( cpca , 489bp ) ,連接蛋白h基因( cpch , 357bp ) ,亞基基因上游啟動子序列( 427bp )以及各基因之間的間隔區( pc - igs , 111bp ; cpch與cpca間隔區, 184bp ) 。According to a 1997 gallup poll, 55 % of scientists ascribe to a completely atheistic evolution, with a total rejection of any deistic involvement
根據1997年蓋洛普民意測驗, 55 %的科學家歸屬于完全無神論進化行列,完全拒絕任何自然神論的的演化。The morphological diagnostic characters for many mature and early instar larvae are still lacking in china. partial sequences of the mitochondrial cytochrome oxydase i and ii and a transfor rna ( co i co ii and trna ) gene of the adults and larvae from caddisflies were. lepidostomaflavum, l. fui, l. arcuatum, paraphlegopteryx morsei, apsilochorema unculatum and apsilochorema hwangi, and the larval and adult stages of these species were sequenced and associated
採用dnastarpackage中的editseq軟體進行序列編輯、 orf查找;採用clustalx軟體進行序列比對( alignment ) ;比對結果輸入mega2 . 1軟體計算各樣品間的遺傳距離,並基於kjmura2 - parameter模型,用鄰接法( neighbor - jojning , nj )構建系統發生樹,通過自展( bootstrap1000次)檢驗獲得系統樹分支的置信度。This arithmetic cast off serial addition idea, but entirely enumerate every pair of addends on a bit. and it also calculate two possible receiving carry value on each bit. so the addition can be operated through automatic selection, and complete collateral addition and carry operation
這種演算法擺脫了以往的串列加法運算思想,將每一位上兩個加數對的所有可能進行全列舉,同時考慮每一位上接受進位值的兩種可能,使得加法運算在自動進行選擇的過程中完成并行的加法和進位。In partridge, chukka, duck, chicken, quail, or others ? 3
在genedoc2 . 3上進行序列比較和同源性分析。Object for serialization and deserialization
對象進行序列化和反序列化。In this paper, through treating lines reciprocal transformation to a matrix, cogradiently reach the eigenvalue and eigenvector of a matrix, to solve the question treat a eigenvalue under without parameters, and given some advanced theorems
摘要通過對矩陣進行行列互逆變換,同步求出矩陣特徵值及特徵向量,解決了不帶參數求特徵值問題,並給出一些新定理。The cloning cdna fragment was extracted from positive clones and sequenced. the results showed that the cdna fragment was 816bp in size, encoding a protein which included 272 amino acids. the sequence homology analysis was carried out via the software blast 2. 0 network service in the four large databases - genbank, embl, ddbj, pdb, which had recorded 1 337 978 nucleotide and protein sequences. the results of the analysis indicated that the nucleotide homologous rates between the rubber tree etr and 15 recorded etrl of other plants ( mango, passion fruit, persia plum, strawberry, grape. . etc ) were 75 % - 80 % ; the protein homologous rates between the rubber tree etrl and these recorded etrl genes were 90 % - 95 %. from the results mentioned above, we could confirm that the cdna of rubber tree etrl had been cloned
從陽性克隆子中提取克隆片段,經序列測定分析,結果表明,克隆片段的cdna大小為816bp ,編碼的蛋白質包含272個氨基酸。基因序列通過blast2 . 0networkservice軟體對genbank , embl , ddbj , pdb四個大型數據庫中記錄的1337978條核酸和蛋白質序列進行序列相似性檢索,結果表明與芒果、一西番蓮、波斯梅、草毒、葡萄、西洋梨等15種已報道的植物的etrl基因cdnag的同源率為75 88 ;蛋白質氨基酸序列的同源率為90 95 ,表明本研究確實克隆到了橡膠樹etri基因的cdna序列。 4The back - exchange process is actually complex and deserving of analysis in a sequence - specific manner
返交換實際上很復雜,需要進行序列特異性的分析。In order to investigate the genomic organization of the single - nucleocapid nucleopolyhedrovirus of helicoverpa armigera, the ecori - n fragment located at 54. 8 - 59. 3 kbp of the viral genome was sequenced. the fragment contained 3762 bp helicase gene potentially encoding a protein with a molecular mass of 146 kda
對棉鈴蟲單核衣殼核多角體病毒( helicoverpaarmigerdsingle - nucleocapsidnucleopolyhedrovirus , hasnpv )基因組中ecori ? n片段進行序列分析,獲得了完整的解螺旋酶基因( hel ) ,其開放閱讀框大小為3762bp ,編碼一個分子量為146kda的蛋白質。分享友人