plate vector 中文意思是什麼

plate vector 解釋
板塊運動向量
  • plate : n 1 厚金屬板 〈cf sheet〉 板(片);(記有姓名等的金屬)牌子,(尤指醫生的)招牌,藏書牌;【印刷...
  • vector : n 1 【數學】向量,矢量,動徑。2 【航空】飛機航線;航向指示。3 【天文學】幅,矢徑。4 【生物學】帶...
  1. In order to express alkaline protease gene ( ap gene ) in bacillus subtil is, the recombinant expression plasmid was constructed. this plasmid contains a promoter bp53, also from b. pumilus un - 31 - c - 42, ap gene and the shuttle vector psugv4. after introduced into b. subtilis wb600, the transformants displayed the hydrolyzed zone on milk plate

    將來自短小芽抱桿菌un一31一c礴2的基因啟動子( bp53片段)和脫毛蛋白酶全基因( ap )進行融合,然後將重組基因(命名為bpap )插入到大腸桿菌-枯草桿菌穿梭質粒載體psugv4中,構建成表達質粒psu一bpap 。
  2. New location algorithm of car license plate using cross - correlation vector map

    基於互相關矢量圖的車牌定位新演算法
  3. Biology, etc. owing to many merits has not yet been used to measure parameters of gratings. the paper researches on the subject in view of current lack of it. the main tasks of the paper include : analyzing ellipsometric characteristics of gratings in detail with vector diffraction theory and ellipsometrics ; devising a reflective quarter wave plate at normal incidence according to some ellipsometric characteristics ; making use of normal simplex algorithm during ellipsometric inversion of gratings parameters, inversing ellipsometric parameters with gaussian noise of different standard deviations to simulate actually measured values with examples of isotropic metallic and anisotropic step gratings and testing that ellipsometry about gratings parameters is feasible with the range of certain precision ; discussing choice of incidence angle at length

    本論文的主要工作包括:結合光柵的矢量衍射理論和薄膜的橢偏理論,詳細分析了光柵的橢偏特性;並且根據一些橢偏特性設計出一款正入射反射型單波長1 4波片;在光柵參數的橢偏反演中,引入正單純形法作為反演演算法,分別以各向同性的正弦形金屬光柵和各向異性的階梯型光柵為例,在標準橢偏值的基礎上加入不同偏差的高斯噪聲來模擬實際的橢偏測量值進行反演,在一定精度范圍內得出滿意的光柵參數,說明光柵參數的橢偏測量是可行的;還就入射角的選取問題進行了一定的探討。
  4. Construction of male sterility expression vector by integration of artificial sense and antisense cdnas of hsp70 into puc18 and puc19 respectively, we can obtain psc and pac. tapertal specific expression promoter ta29 and terminator nos are connected directionally with sense and antisense cdnas of hsp70 extrected and purified from psc and pac., then integrated into puc18 and puc19, by which we can build sense and antisense cdna nos ( respectively named plasmid 650 and plasmid 651 ) of ta29 - hsp70. for the sake of better screening and examination of transformed gene, we cut plasmid 650, plasmid 651 and 3301 ( containing gusgene bar screening marker gene ) with hindiii and ecor i enzymes, then connect purified fragments of 650and 651 with plasmid 3301 to construct the vector 3301 + 650 and 3301 + 651. corroboration of whether sense and antisense cdna - nos is integrated into plasmid3301 can be made by plate screening and enzye - cutting analysis

    分別將從psc 、 pac回收純化的hsp70正、反義cdna與絨氈層特異表達啟動子ta29及nos終止子定向連接,然後插入到puc18 、 puc19中,構建成花藥特異表達的ta29 - hsp70sensecdna - nos和ta29 - hsp70antisensecdna - nos ,分別稱作650和651質粒。為了更好地對轉化子進行篩選和檢測,用hind和ecor分別對650 、 651及3301質粒(含gus報告基因和bar篩選標記基因)進行酶切,將從650和651回收純化的目的片段與3301質粒進行連接,再對重組子進行平板篩選和酶切分析確定ta29 - hsp70sensecdna - nos和ta29 - hsp70antisensecdna - nos插入到3301質粒中,構建成3301 + 650和3301 + 651表達載體。
  5. The solutions include : the unit normal vector of the elastic - plastic boundary near the crack line, the elastic - plastic stress fields near crack line, law that the length of the plastic zone along the crack line is varied with an external loads, the maximum lengths of the plastic zone, the bearing capacity of a finite plate with an eccentric crack loaded by shear forces

    這個解包括:裂紋線附近彈塑性邊界上的單位法向矢量,裂紋線附近的彈塑性解析解、最大塑性區長度、裂紋線上的塑性區長度隨荷載的變化規律及其承載力。
  6. The interesting gene fragment with ecori and noti were amplified by overlapping pcr, which inserted into vector plasmid ppic9k after degisted by ecori and noti, and the recombinant plasmid was transformed into competent dh5cc. positive clones were screened by pcr from the lb plate with amp. digesting analysis resulte shows that the interesting gene were inserted into the vector ppic9k with correct direction

    目的基因經雙酶切后連接載體ppic9k ,然後導入大腸桿菌dh5中,在含氨卞青霉素( amp )的lb板上用pcr反應篩選出陽性菌落,雙酶切結果表明目的基因已插入載體中,且方向正確,測序結果進一步證明人巨細胞病毒重組基因表達質粒成功地克隆了目的基因片段。
  7. After electrophorised on 1 % agarose gel, the pcr production was purified with agarose gel dna extraction kit. the segment was ligated with vector pmd18 - t and then was tranformed into the competent cell of dh5 a. a construction mstnd - pmd18t was generated by inserting the sequence of 254bp into pmd18 - t vector and selecting the sense clones. positive clone was identified by three ways : endonuclease digestion, pcr and sequencing. the result showed that the cloned sequence coincides with the designed sequence. this construction was digested with nco i and xho i and ligated the pet28a ( + ) vector digested with the same enzymes using dna ligation kit. the production of ligation reaction was transformed into the competent cell of bl21 ( de3 ). after 12 - 16 hours of culture, several colnes appeared on the plate. some positive clones were selected to extract their plasmid. these plasmids were digested by nco i and xho i and indentified by pcr. a contraction, mstnd - pet28a was generated. the result showed that the cloned sequence coincides with the designed sequence

    F _ 1長38bp , r _ 1長36bp ,其它片段均40bp長, f _ 1和r _ 1片段兩端分別加上限制性內切酶nco和xho的識別位點序列。用成對單鏈片段進行延伸反應,然後用其他單鏈片段作為引物,進行pcr擴增,用dna快速純化回收試劑盒回收所得254bppcr產物,與pmd18 - t載體連接、轉化dh _ 5 。受體菌感受態細胞,利用藍白斑遺傳學篩選法篩選陽性克隆,提取其質粒,採用nco和xho雙酶切鑒定,獲得了254bp的片段;用pmd18 - t載體上的特異引物rv - m和m13 - 47進行pcr鑒定,獲得300bp的片段。
  8. Using the similarity between plane elasticity and plate bending, this paper successfully fulfils the identification of rolling vector and establishes a general method, the curvature lumping method, to represent the rolling vector by the use of simple displacements vector

    利用平面彈性和板彎曲的相似性,本文實現了角卷向量的辨識並得到了用簡單位移向量表示角卷向量的一般方法?曲率堆集法,打通了與有限元通用程序的介面。
  9. The main work is as follow : the pater makes use of vanguard genetic algorithms in image segmentation, uses vanguard genetic algorithms to get the image threshold. using this method we may get different grey vehicles from the background exactly. used the support vector machine theory to conduct the vehicles automatic sorting simulation research, the simulation result had proven this method could quite be accurate carries on the vehicles type the recognition ; improved based on the background automatic renewal hypothesized examination region algorithm, enhanced timeliness and the accuracy which the vehicles examines ; and to has carried on the specify based on the hypothesized examination region imagery processing algorithm realization ; in the paper also introduced withdraws the algorithm based on the gradation continuous movement vehicles characteristic to carry on the vehicles the characteristic to withdraw as well as to use the localization method which colored filter same gradation chart processing unifies to carry on the realization method which the vehicles license plate locates

    本文根據智能交通控制與模擬對于交通流量、車輛到達率、車輛速度等交通信息檢測的需求,基於視頻圖像進行了交通信息處理的演算法研究與實現,主要工作包括以下幾個方面:將先鋒遺傳演算法應用到圖像閾值分割中,利用先鋒遺傳演算法尋求全局最優閾值,可以比較準確的將圖像中不同灰度的車輛從背景中分離出來;採用支持向量機理論進行了車輛自動分類的模擬研究,模擬結果證明該方法能夠比較準確的將車輛的類型進行識別;改進了基於背景自動更新的虛擬檢測區域演算法,提高了車輛檢測的實時性和準確性;並對基於虛擬檢測區域的圖像處理演算法實現進行了詳細說明;論文中還介紹了基於灰度連續性的運動車輛特徵提取演算法進行車輛的特徵提取以及採用彩色過濾器同灰度圖處理相結合的定位方法進行車輛牌照定位的實現方法。
  10. The ubi - sl - tocs fragment was taken out, inserted into the multi - cloning site of pcambia1300 vector, transformed into jm109 strain finally, positive colonies were screened on lb plate ( 60 g / ml kan added ). the result of pcr and enzyme digestion of plasmid proved that recombinatin vector was obtained ( named pcusaib4 and pcusaibu )

    把擴增產物分別通過clai和bamhi酶切純化,連接到用clai和bamhi切去gfpml基因的中間表達載體pugfpocs中,轉化大腸桿菌jm109 ,在含amp ( 100 g / ml )的lb抗性平板上篩選到了的陽性菌落。
  11. The recombinant expression vector ppic3. 5kv with vgb gene was used to transform the pichia pastoris gs115 / ppic9m via electroporation, yeast strain pichia pastoris gs115 / ppic9m / ppic3. 5k containing the integrated monellin gene and vgb gene was obtained by g418 ( 0. 5mg / ml ) plate

    進一步通過電擊轉化將vgb基因整合到重組酵母gs115 / ppic9m的基因組中,獲得了由高甜度monellin和vgb兩個基因同時整合的重組酵母gs115 / ppic9m / ppic3 . 5kv 。
  12. First, the conducting targets ' electromagnetic scattering is researched in this paper. the rwg vector base functions are used to denote inductive current on the surface of the conducting target. efie is built. the rcs of conducting sphere. conducting plate, conducting cube are calculated respectively, the electromagnetic scattering of multi - rivets on the conducting plate are researched the first time, and the impaction of multi - rivets to the total rcs is analyzed

    用rwg矢量基函數表示導體表面的感應電流,建立了導體表面的電場積分方程( efie ) ,分別計算了導電球、導體平板、導電立方體的rcs ,首次研究了導電平板上有多個鉚釘的電磁散射,分析了多個鉚釘對目標總的rcs的影響。
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