識別因子 的英文怎麼說
中文拼音 [zhìbiéyīnzi]
識別因子
英文
recognition factor- 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)
- 因 : Ⅰ動詞[書面語] (沿襲) follow; carry on Ⅱ介詞1 [書面語] (憑借; 根據) on the basis of; in accord...
- 子 : 子Ⅰ名詞1 (兒子) son 2 (人的通稱) person 3 (古代特指有學問的男人) ancient title of respect f...
- 識別 : 1 (辯別; 辯認) discriminate; distinguish; discern; tell the difference; spot 2 [計算機] identif...
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Identifying the fittest factor analysis model with aic criterion
準則識別最佳因子分析模型It has been established the existence of a few pathways controlling flowering of plants in genetic research of flowering of arabidopsis thaliana and antirrhinum majus. many genes related to flowering have been identified and cloned, but the regulation mechanism of gene ' s expression is still unclear
通過模式植物擬南芥和金魚草開花機理的研究,現在已經明確植物的開花途徑有多條,並識別和分離了許多與開花有關的基因,但這些基因如何在植物生長發育過程中進行特定時空的表達及其調控一直是科學家研究的一個黑匣子。The approximation analysis result of band dipole model is obtained on the basis of the theory of mfl. the electromagnetic distribution feature of the defect in the steel panel is studied by means of simulation. the leakage magnetic distribution of the two defects and four defects plural and the defects in the column differently in the width are also assayed. conclusions that factors affecting flaw magnetic leakage to the panel also affect the column and magnetic leakage bx should be the feature of the flaw identification to several flaws are drawn
在對漏磁檢測原理進行詳細介紹的基礎上,得出了帶偶極子模型的近似解析解,並以有限元數值模擬分析為主要手段,以鋼板上缺陷為對象,分析了各因素對缺陷漏磁場產生影響的不同規律,同時模擬分析了板上平行的兩條裂紋,四條裂紋以及柱體上寬度不同時的裂紋的漏磁場分佈特徵,得出結論:影響板上缺陷漏磁場的諸因素會對柱體上缺陷漏磁場產生同樣的影響;對于多條裂紋,宜用漏磁分量bx作為缺陷識別的特徵量。Three different momentnormalization methods have been used, two of which are based on affinemoment normalization technique and the third is based on reducing theaffine transformation to a euclidian transform
三維紋理的光照不變性識別是一個很復雜的問題,這是因為對光照和仿射變換的不變因子推導是十分困難的。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。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)。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) 。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 。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。Part 3 : the paper set out from big system and coordination view, use the systematic dynamics method to analyse all - sidedly that the city expands the relation with various kinds of ecological factors, and natural factor discern mode of city develop, point out city ecological problems are production by improper use the environment ecological factor during city expand, it cause the problems production, such as the function of natural system disappearance or lose efficiency ; systematic circulation obstruct, material energy transform efficiency being low, and so on
第三部分:從大系統大協調觀出發,運用系統動力學方法全面分析城市擴展與各種生態因子的因果關系,及城市發展的自然因子識別模式,指出城市生態問題的產生是由於城市擴展對環境生態因子的不當使用,導致自然系統功能的缺失或失效,系統循環受阻,物質能量轉化效率低下等問題的產生。Using molecular imprinting method, the 1, 3 - dimethylxanthine theophylline, tho molecular recognition membranes, containing an segments as membrane formation sites and aa segments as functional sites, were prepared by the phase inversion technique. here, tho was selected as a template molecule. the hydrogen bonding between aa segments and the tho templates was measured by ft - ir and nmr. the tho templates can be removed from the membrane through washing with acetic acid aqueous solution. the permeation of tho through the membranes is far more than that of 1, 3, 7 - trimethylxanthine caffeine, caf, which demonstrated the function of tho molecular recognition of the membrane. the results also show that the increase of the tho templates concentration in the cast solution caused an increase of tho amounts taken into the copolymer membrane
Ft - ir及nmr測試結果表明:制備的高分子膜中, tho模板分子和膜中的丙烯酸功能殘基存在著氫鍵鍵合作用。大量的極性醋酸水溶液可抽出膜中的模板分子。 tho溶液和與模板分子具有相似結構的1 , 3 , 7 -三甲基黃嘌呤咖啡因, caf溶液的基質透過實驗結果:進入膜結構中tho分子的量遠大於caf分子,這表明制備的高分子膜具有tho分子識別功能。Age as one of the internal factors can affect the value of venturous revenue through acting on the checking results of the external factors ( e. g., predation pressure ), and thereby affect the optimal migrating strategies. therefore, the patterns for dvm vary with the change of the animal ' s age
作為內部狀態因子的年齡,因對外部因子(如捕食壓力)識別結果的影響而對風險收益值有較大的影響,從而影響橈足類垂直遷移的最佳策略,導致其遷移的形式隨年齡的變化而變化,一般來說,年齡越大的動物垂直遷移的時間越早、幅度越大; 3Phishing e - mail is hard to identify, because attackers make their e - mail appear genuine and often mimic recognizable e - mail sent out routinely by legitimate organizations such as banks and credit card companies
網路仿冒電子郵件很難識別,因為攻擊者將他們的電子郵件偽裝得很真實,並經常模仿合法組織如銀行和信用卡公司經常發送的用戶熟悉的電子郵件。After the recombinant plasmid pcdna3. 1 / ts87 was identified by digestion of hindlll and bamh i, it transformed into cos7 by lipofectamine. expression product was identified by immunohistochemical method, sds - page and western - blot. the immunocytochemistry result has shown that specific brown - staining grains were found in the cytoplasm of cells transformed by recombinant plasmid versus not seen in cells transformed by pcdna3. 1 or normal cells ; the sds - page result has revealed that a band about 3 8kb was found in cell lysis transformed by recombinant plasmid versus not in cells transformed by pcdnas. l or normal cells ; the western - blot result has showed that only the band about 38kd was recognized by sera from rabbit infected by t. s artificially and sera from rabbit immunized with soluble antigen of t. s and with protein expressed by ts87 gene and by a monoclonal antibody of t. s
通過細胞的免疫組化,細胞裂解物的sds - page電泳, westem - blot分析檢測目的基因的表達情況。免疫組化結果顯示:重組質粒轉染的細胞質中有棕褐色顆粒,而空載體轉染細胞及正常細胞無此現象;細胞裂解物sds - page電泳結果顯示:只有重組質粒轉染的細胞在約38kd處有明顯的蛋白帶,這與理論計算的ts87基因表達蛋白的分子量為38kd基本一致; western - blot分析結果顯示:約38kd的蛋白帶能夠分別被旋毛蟲感染兔血清,成蟲蟲體可溶性抗原免疫兔血清, ts87基因原核表達蛋白免疫兔血清( ts87血清)以及一株具保護性的旋毛蟲單抗特異識別。Structural matching is a main approach for on - line chinese character recognition. in order to reduce its great computational comple xity and improve its performance, people have been seeking for a way to guide the whole matching by the result of partial matching. in this paper, the authors prop osed 45 basic components from 3, 755 categories of the daily - used chinese charac ters to guide the stroke segment matching. because they always locate at either the beginning or the end of the stroke segment string, these components are easy to extract and separate from other parts of the character. besides, the reference templates of these components are dynamically extracted from the reference segmen tstring and dependent on the current matched character so that a more accurate matching is carried out. experiments show that the segment matching computation h as reduced almost 50 %. the approach is also enlightening for other similar object matching problem
結構匹配是一種有效的聯機手寫漢寫識別方法,為了減少匹配運算,人們一直在尋求利用部分匹配的結果來引導整體匹配的方法.在特徵匹配與結構匹配綜合的基礎上,從3 . 755個一級國標漢字中提取出45個子結構,利用它們來引導結構匹配.由於這些子結構總出現在字首或字尾,因而對它們的檢測比較容易.同時,通過建立子結構活動模板及設計子結構動態抽取演算法,使得子結構匹配的準確度得到很大提高.實驗結構表明,該方法使結構匹配的運算量減少約50 % ,並對類似的物體識別問題有一定的啟發意義3 wang l, healey g. using zernike moments for the illumination andgeometry invariant classification of multispectral texture. ieeetrans. image processing
三維紋理的光照不變性識別通過構建zernike矩不變因子矩陣,然後利用奇異值分解方法來計算區分因子解決。The dvm behavior of the copepod is controlled by multi - factors. the diversified migrating patterns show that copepod is the active decision - maker, which can achieve the optimal food intake during its avoiding predation by performing the normal dvm ; 2
足類的晝夜垂直遷移行為是由多因子控制的,其遷移模式的多樣性表明,橈足類是主動的決策者,通過識別環境因子的變化,橈足類藉助于常規的晝夜垂直遷移在逃避捕食壓力的同時能夠實現最優的食物攝取量; 2According to the data of drilling and other geological investigation on the lpg storage of jinzhou, and taking into account main factors that affecting stability of the storage and other classification standard, this paper selects five evaluating factors. using pattern recognition method and muti - step fuzzy classification clustering method to classify
根據錦州lpg洞庫的地質勘察資料,考慮到影響洞庫圍巖穩定性的主要因素,結合已有的分類標準,本文選取了5個評價因子,用模式識別法與多級模糊聚類法來進行場地巖體的穩定性分類。Dendritic cells ( dc ) is the most powerful apc, which can markedly increase the antigen - presentation capacity by maximizing the pepitide - mhc complexes on the cell surface and upregulating the co - stimulatory ligands b7 - 1 and b7 - 2, adhesion moleculees such as il - 12 that promote full activation of lymphocytes. full activation of antigen - specific t cells requires two signals - one signal coming via the tcr and the other signal through engagment of co - stimulatary molecules. t cells receiving one signal via their tcr are turned off by mhc ( major histocompatibility complex ), via t cell cd28 binding to b7 on the dc induce tlymphokine and t cell proliferatiion
T細胞介導的細胞免疫在控制腫瘤生長方面發揮著重要作用, t細胞在發揮抗瘤效應(分泌細胞因子和直接殺傷)之前必須先經過活化,體內專職抗原提呈細胞( apc )細胞並使其活化,樹突狀細胞( dendriticcell , dc )為t細胞的激活提供雙重信號, t細胞藉助tcr識別由dcmhc分子遞交的抗原肽后,通過tcr - cd3復合體傳遞抗原特異性識別信號(第一信號) ,以cd28為主的t細胞表面輔佐分子識別dc表面b7分子,傳遞非特異性協同刺激信號(第二信號) ,在機體抗腫瘤免疫應答中處于核心地位。Therefore, the determination of seb is very important for food hygienic analysis as well as for clinical analysis. nucleic acid hybridization technique is one of the widely - used methods in molecular biology and gene technology. the present work has developed piezoelectric biosensors used in the detection of seb dna by tacking the piezoelectric quarts crystal as a sensitive component while synthetic oligonucleotide probe as recognize molecule
其中b型葡萄球菌腸毒素( seb )是一種通常條件下更穩定,毒性最強的毒素,而核酸雜交技術則是分子生物學和基因工程中最常用和最基本的方法之一,因此本論文以該毒素的產毒基因為檢測對象,以壓電石英晶體為敏感元件,以合成的寡核苷酸探針為識別分子,構建了用於seb基因檢測的壓電生物傳感器。分享友人