瞬時表達 的英文怎麼說

中文拼音 [shùnshíbiǎo]
瞬時表達 英文
transient expression
  • : Ⅰ名詞(眼珠一動; 一眨眼) wink; twinkling Ⅱ動詞(眨眼) wink
  • : shí]Ⅰ名1 (比較長的一段時間)time; times; days:當時at that time; in those days; 古時 ancient tim...
  • : Ⅰ名詞1 (外面;外表) outside; surface; external 2 (中表親戚) the relationship between the child...
  • : Ⅰ動詞1 (暢通) extend 2 (達到) reach; attain; amount to 3 (通曉; 明白) understand thoroughly...
  • 表達 : deliver; express; show; voice; convey; communicate
  1. The transient expression of mgfp4 in rice calli

    4在水稻愈傷組織中的瞬時表達
  2. We generated a recombinant eukaryotic gene expressing vector harboring a full - length hgh gene, 2. 4 kb genomic dna with four introns and the signal peptide sequence cloned to the eukaryotic gene expressing vector pcdna3. 0

    我們直接將含有4個內含子和自身信號肽的2 . 4kb全長人生長激素基因直接克隆至真核載體pcdna3 . 0 ,然後利用脂質體轉染家蠶bmn細胞,瞬時表達hgh 。
  3. The equations of motion governing the axisymmetric elastic deformation of finite orthotropic cylindrical shells, involving the effect of transverse shear and rotational inertia, are derived. by applying the reverberation method, the displacement and the resultant forces of the shell in the phase space are expressed. then the transient waves in the finite orthotropic cylindrical shell subjected to the axisymmetric impact are obtained by using inverse laplace transforms. furthermore, the transient solutions are decomposed to the generalized ray integrals and computed numerically

    分析了計及剪切變形和轉動慣性的有限長正交異性圓柱殼中彈性態波的傳播問題,採用回傳矩陣法,在相空間中給出了位移和內力的式。再利用laplace逆變換,得到正交異性圓柱殼受軸對稱沖擊作用彈性態波解,然後將其分解為若干廣義射線積分之和,並用數值方法求解之。
  4. After a sabbatical from film - making to become a mother in 1994, binoche was selected as the heroine of france s most expensive 35 million movie ever : hussard sur le toit, le 1995. more recently she has made english patient, the 1996, for which she won an oscar for best supporting actress and chocolat 2000

    迄今為止,她主演的所有影片都是有關愛情的,她在燃燒在心靈深處的愛情,不是通過強烈的外部動作,而是通過脈脈含情的眼神含蓄雋永的語言在不經意的間完成的,這種富有節制的演往往比完全外露的情感更強烈更深刻更耐人尋味。
  5. The expression efficiency difference between ped5 and pcdhfrl, a vector utilizing cmv enhancer / promoter ( pcmv - ie ) for foreign protein production, was analyzed using human interferon - p ( ifn - ) gene and human secreted alkaline phosphatase ( seap ) gene as reporters. when analyzed in transient expression, ped5 showed a little more protein produciton than pcdhfrl. however, in continuous expression, when serum concentration was lessened to slow down cell proliferation, ped5 expressed 3. 1 times more reporter proteins than pcdhfrl, which implied that pef - io was less affected by cell cycle status in contrast to pcmv - ie, making ped5 a good expression vector for foreign protein production

    應用人-干擾素( ifn - )和人分泌型堿性磷酸酶( seap )基因作為報告基因,對含有巨細胞病毒即早期啟動子( p _ ( cmv - ie ) )的載體pcdhfr1和ped5外源蛋白的能力進行了比較,發現對于瞬時表達, ped5略好於pcdhfr1 ;在穩定中,通過降低血清濃度,使細胞增殖緩慢,這ped5外源蛋白的能力較pcdhfr1高3 . 1倍。
  6. Transient expression of fibrillin promoter in protoplasts of arabidopsis thaliana and brassica napus

    操縱子在甘藍型油菜和擬南芥中的瞬時表達
  7. 4. after having established genetic transformation system with tomato cotyledons as explant and determined the transformable of preculture time, incubation time and co - culture time, we set up the system of high frequency transformation of tomato cotyledons. then hbmp - 3m gene was transferred into tomato via agrobacterium - mqdiated transformation, and the resistant plants to hyg were obtained. by pcr analysis on part of the putative transformants, we identified that hbmp - 3m gene had been integrated into the genome of part of tomato plants. 5. transferred hbmp - 3 gene into tobacco via agrobacterium - mediated transformation and obtained the resistant plants to hyg. trans genie tobacco plants were confirmed by instantaneous expression of gus gene in calli detection, growth and bio - morphology analysis, hyg - resistant experiment and pcr analysis

    通過pcr檢測證實部分番茄抗性植株中已導入hbmp - 3m基因;人骨形成蛋白一3成熟膚基因和全長基因分別轉化番茄和煙草的研究5 .通過農桿菌介導法將hbmp一3全長基因導入煙草,並且獲得了hyg抗性植株,通過gus基因瞬時表達檢測、轉化植株的生長情況及形態學分析、 hyg抗性鑒定及pc尺檢測,證明目的基因己經整合到煙草基因組中。
  8. This result showed that gus was transiently expressed in the foliage, and they were of laticifer - expression

    因此認為gus基因在葉片成功的實現瞬時表達,而且具有乳管活性。
  9. To identify its laticifer - expression character, two transient - expression vectors ( pirl, pbir2 ) were constructed. in the transient - expression vector, ref promoter sequence replaced camv35s promoter of pbi121

    為驗證其乳管活性,通過取代pbi121中間載體上的camv35s啟動子,構建了兩個含gus基因的瞬時表達載體pbir1 、 pbir2 。
  10. Rt - pcr showed that the gfp transcripts from wild type nicotiana benthamiana inoculated with the tnos deletion vector lacked a normal poly ( a ) tail

    接種野生型本生煙后的rt - pcr結果明, gfp - atnos載體瞬時表達所產生的gfprna可能沒有poly ( a )尾序。
  11. I have used low copy pbin19 and single copy pmw755i5j binary vectors as backbone plasmids, to create a gene targeting insertion vector designated gfp tnos. after agro - infiltration into transgenic nicotiana benthamiana 16c, progeny were analyzed genetically for phenotypic changes, sirna accumulation, and dna methylation

    採用農桿菌浸潤法( agro - infiltration )感染轉基因本生煙16c ,並對同源基因瞬時表達所引起的植物型變化、小分子rna的產生、 dna甲基化程度、以及相關性狀在後代中的遺傳情況進行了檢查。
  12. 3, 4, 5 and ? 6 of this chapter deal respectively with the transient distribution of the queue length of these four queueing systems. such results are obtained as follows : under the condition of the interarrival times distributions and service times distributions of these queueing models which have density function, their transient distribution of the queue length can be represented as an integral, and the integrated term of this integral can be recursively obtained

    在這一章的誇3 、芬4 、縣5和號6中,分別針對這四個排隊模型,討論了隊長的分佈,最終得到了以下的結果:在這幾個模型的到間隔分佈和服務間分佈均具有密度函數的條件下,它們的隊長分佈可以示為一個積分,該積分的被積項可以遞歸地求取。
  13. In the first part, the focus is to find the receptor molecules directly by screening two cdna libraries with a recombinant construct prpap or as an alternative, to find an enriched area in the embryo brains and construct libraries from this brain region and perform the expression cloning as above

    方法: ( )以融合蛋白prpap通過瞬時表達克隆法篩選兩個cdna文庫,或者通過與胚胎腦的結合實驗篩選有豐富結合蛋白的腦區,以圖構建cdna文庫並進行克隆的篩選。
  14. An on - line minimum - variance estimator was developed for thrust acceleration applied to orbit transfer using discrete - time radar measurements. the mass - flow - rate of propellant was selected as a state variant, which was estimated by employing an integral state model and ekf filter. the variation equations for measurement vector to mass - flow - rate have been established to linearize the discrete - time measurement equations. the algorithm has applied successfully to maneuver process in commanding satellite into geo - stationary orbit. the results show that the algorithm developed here can monitor and determine whether engine works well or failure precisely and quickly during orbit transfer process

    飛行器軌道機動過程中,為跟蹤、定位機動目標和干預機動控制過程,需要統計處理離散的雷觀測量實估計推進發動機的推力,進而確定飛行器的軌道參數.本文所述演算法是該工程問題的探討和解決方案.文章建立了軌道機動過程中連續變質量運動模型和離散雷量測模型,推進發動機的質量秒耗量作為徵推力加速度的一個近似常量,應用擴展卡爾曼濾波對離散的雷測量數據進行順序統計處理給出秒耗量的最小方差估計;文章詳細地推導了線性化量測模型的變分方程和觀測矩陣;模擬結果明該演算法能快速、準確地估計推進發動機的質量秒耗量和向機動目標施加的實際推力
  15. 2. construction of chimeric mtb8. 4 / hil - 12 eukaryotic expression plasmid ( 1 ) construction of pci - neo - mtb8. 4 - linker ( pml ) and pci - neo - ms - linker ( pmsl ) mtb8. 4 - linker and ms - linker gene ( without stop codon ) were pcr amplified by using two oligonucleotides designed to generate nhe i and mlu i restriction sites at the 5 " and 3 " ends of the amplified fragments, respectively

    3 .重組質粒在真核細胞中的: pm 、 pms 、 pmi和pmsl重組質粒用lipofectaminatmzo0o脂質體轉染試劑轉染cos一7細胞,進行瞬時表達, 48小后,用rl 』 - pcr檢測目的基因在mrna水平的;用westemblotting檢測hil一12在蛋白質水平的
  16. ( 2 ) deletions of four different lengths were conducted using pcr amplification with the information of sequence of pdf 1. 2 gene promoter. these mutated promoters were fused to the gus reporter gene and introduced into tobacco plants. the results of gus activity driven by these different constructs showed that the promoter sequence between positions - 300 and - 243 ( containing a gcc box and a g box - like sequence ) was an essential ja - responsive element region to activate the expression of gus reporter gene, and the - 300 bp position was defined as the boundary of the minimal functional promoter in response to ja signaling

    ( 2 )對該啟動子的5 』端進行不同長度的缺失突變,突變的啟動子與gus構建的融合基因在煙草中受meja誘導的瞬時表達結果明,該啟動子中- 300 - 243bp區域(有一個gccbox和一個gbox - likesequence )是其應答meja處理所必須的區域,並將- 300bp作為該啟動子應答ja信號的最小區域的邊界位置。
  17. ( 3 ) on the basis of the deletion analysis, three substitution mutants ( ml : 6bp sequence upstream of gcc box m2 : gcc box and m3 : g box - like sequence ) by pcr were designed to isolate the essential ja - responsive element. transgenic tobacco plants containing promoter substitution constructs were generated by agrobacterium - rnqdiaied leaf transformation. loss - of - function experiment, using transient expression analysis of gus reporter genes, confirmed that gcc box act as an essential element to respond ja signaling in pdf1. 2 promoter

    ( 3 )在缺失突變的基礎上,通過對gccbox及其相鄰的上下游六個堿基進行取代突變,將突變啟動子與gus構建融合基因,在煙草中受heja誘導的瞬時表達結果明, h1和m3的突變對該啟動子應答ja信號的影響很小,而m2 ( gccbox的突變)則幾乎使該啟動子應答ja信號的功能完全喪失,所以gccbox是該啟動子中應答ja信號的必需元件。
  18. Acetosyringone ( as ) can increase the gus gene transient expression when it was added in the suspending medium

    在菌液中添加as可以提高gus基因的瞬時表達
  19. Pre - cultured 2 days and co - cultured 6 days can also enhance the efficienty of transformation of torenia fournieri lind

    預培養2d后共培養6d ,可以明顯增加gus基因的瞬時表達和不定芽的形成。
  20. The ha 122 protein, when fused to gfp was observed in the nuclei of h. armigera cells, but only in conjunction with wild type hasnpv infection

    將ha122與綠色熒光蛋白( gfp )基因融合,在昆蟲細胞中瞬時表達。當有病毒感染同發生, gfp信號定位在核內。
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