sequence n. 1.繼續(xù);接續(xù);連續(xù)。 2.順序;程序;次第;關(guān)系;關(guān)聯(lián)。 3.后果;結(jié)果;接著發(fā)生的事;后事;后文。 4.【數(shù)學(xué)】數(shù)列;序列;數(shù)貫。 5.【無、計(jì)】指令序列;定序。 6.【計(jì)算機(jī)】順序機(jī)〔將信息項(xiàng)目排成順序的機(jī)器〕。 7.【音樂】用不同音調(diào)反復(fù)演奏一組樂句。 8.【天主教】宣講福音前唱的圣歌。 9.【牌戲】順。 10.【電影】(描述同一主題的)連續(xù)鏡頭;片斷,插曲;場(chǎng)景。 a logical sequence 條理;邏輯順序。 a causal [physical] sequence 因果關(guān)系。 the natural sequence to [for] folly 愚笨行為的必然結(jié)果。 in rapid sequence 一個(gè)接著一個(gè);緊接著。 in regular sequence 挨次;按次序;逐一;有條不紊地。 in sequence 挨次;順次;逐一。 sequence of tenses 【語法】時(shí)態(tài)的配合[接續(xù),呼應(yīng)]。
The recombinant transfer vector pbacpak - hbmp was constructed by insertion of the hbmp coding sequences into the multiple cloning site of transfer vector pbacpak . 8 . bmn cell line was co - transfected with pbacpak - hbmp plasmid and linearized baculovirus bacpak6 dna by dosper agent 將克隆到的hbmp基因通過適當(dāng)?shù)拿盖胁迦氲睫D(zhuǎn)移載體質(zhì)粒pbac - pak8的多克隆位點(diǎn)中,獲得重組轉(zhuǎn)移載體質(zhì)粒pbacpak - hbmp 。
Based on the single cycle detector , the finite cycle detector is proposed for the detection of phase - coded signals . the finite cycle detector has a good performance under unknown the spreading code sequence , initial phase , spreading code timing epoch 針對(duì)相位編碼信號(hào)的檢測(cè),提出了基于單循環(huán)檢測(cè)器的有限多循環(huán)檢測(cè)器,可在沒有編碼序列、初相、編碼序列初始時(shí)間等信息的情況下,取得理想的檢測(cè)效果。
On the basis of the composition of a file , the sequence of significant code sequences or based on particular behavior patterns , the heuristics can determine with a high probability whether it is dealing with a harmful or virulent file 在文件的基層結(jié)構(gòu)(不知道怎么翻譯- _ - | | ) ,有意義代碼的順序或者基于特殊的行為特征(還是不知道怎么翻譯- _ - | | ) ,有很高的幾率可以啟發(fā)出文件是否是一個(gè)有害的或者含有病毒的文件。
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 本文提出了基于糾錯(cuò)編碼的svm多類分類算法( ecc - svm ) ,并分析了ecc - svm的推廣能力與編碼長(zhǎng)度、碼間漢明距離、編碼順序以及分類間隙等之間的關(guān)系,給出了這種關(guān)系的數(shù)學(xué)描述。
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(jìn)行誘導(dǎo)表達(dá),以sds一page分析fasl胞外區(qū)的表達(dá)。
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(gè)堿基,獲得了融合乙肝表面抗原中蛋白基因( hbmp ) 。
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(zhǎng)編碼區(qū)的dna序列構(gòu)建的nj圖,最簡(jiǎn)約樹與用其3 ’端編碼區(qū)dna序列構(gòu)建的樹形圖相同,表明完全可以用epsps基因3 ’端編碼區(qū)dna序列代替基因全長(zhǎng)編碼序列作進(jìn)化分析。
Hla - g1 , which is a newly defined non - classical hla class i molecule , plays an important role in mediating immunotolerance and protecting embryo and even some kinds of tumors from nk cells attacking . the full - length coding sequences containing cdna of hla - g1 were cloned from placenta , monocytes and liver cancer tissue of chinese donors . sequence analysis reveals that it is a highly conserved human gene with only two amino acid mutation sites compared to foreign nationality . its truncated form was overexpressed in 從中國(guó)人外周血單個(gè)核細(xì)胞胎盤組織和肝癌組織等樣品中克隆了包含完整hla - g1讀框的cdna與國(guó)外同行獲得的該基因及其蛋白質(zhì)序列比較分析表明,該基因雖然有著細(xì)微的種族特異性,但高度保守并獲得了它的截?cái)嘈椭亟M蛋白,根據(jù)蛋白一級(jí)結(jié)構(gòu)和同源比較方法,模建了它及其與特異性受體kir2dl4形成復(fù)合體的空間結(jié)構(gòu)模擬,預(yù)測(cè)了它們之間相互作用的特征。
The coding sequence of the two full - length cdnas were cloned by pcr , and inserted into expression vector pmet a between the downstream of a secreting signal peptide and the upstream of 6x histidine in the same reading frame with the coding sequence . the secreting recombinant expression vectors pmet a b / abp2304 and pmet a a / abp780 were constructed and transformed into pmad16 with lici transformation 利用pcr技術(shù)將上述兩個(gè)全長(zhǎng)cdna的編碼區(qū)克隆到表達(dá)載體pmet上,使之位于因子信號(hào)肽序列的下游, 6個(gè)組氨酸殘基序列的上游,且與之同框,分別構(gòu)建成融合蛋白分泌表達(dá)載體pmet b abp2304和pmet a abp780 。
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(qū)全長(zhǎng),其中前20個(gè)氨基酸的g + c含量按暨南大學(xué)碩士學(xué)位論文:大腸桿菌表達(dá)重組hbfgf結(jié)構(gòu)和功能優(yōu)化摘要照計(jì)算機(jī)軟件計(jì)算的結(jié)果進(jìn)行了調(diào)整,第78和96位上的半瞇氨酸被突變?yōu)榻z氨酸。