轉位因子 的英文怎麼說
中文拼音 [zhuǎnwèiyīnzi]
轉位因子
英文
transposable elements-
Inertial instability barotropic advection of potential vorticity the subsidence of the large value of potential vorticity above cyclone and geostrophic adjustment process is dynamical factors which make the cyclone developed violently
慣性不穩定,正壓位渦平流以及正壓位渦大值下沉至氣旋上空和地轉適應過程是氣旋強烈發展的動力因子。Transposable elements, or insertion elements, are dna sequences which can be inserted into many different sites in chromosomes.
轉位因子或插入因子是能夠插入到染色體不同位點的DNA序列。Transposable elements, or insertion elements, are dna sequences which can be inserted into many different sites in chromosomes
轉位因子或插入因子是能夠插入到染色體不同位點的dna序列。" viruses, plasmids, and transposable genetic elements. " chap 6. in molecular biology of the cell. pp. 273 - 8
細胞內的分子生物學第六章病毒、質體,與轉位基因元件。第273到278頁。Thiscould be transcriptional binding sites for example. proteins such asfluorescently labeled dna - binding transcription factors in solution areadded to the chip and incubated on the array
這可以轉錄結合位為例.蛋白質等熒光標記dna結合轉錄因子溶液加入關于陣列晶片及孵化This algorithm is based on the 16 - fft about square root decomposition, and using the phase revolution unit replaces multiplication, and uses the serial butterfly operation unit. at last, gives the correspond realization measure in fpga
本文根據一種基於平方根分解的16點fft演算法,採用相位旋轉因子取代乘法器,並利用串列流水蝴蝶運算單元給出了一種新的實現演算法,並介紹了其在fpga中相應的實現方法。Histochemical staining in tl transgenic tobaccos showed that sigp1 promoter was not only organ - specific ( especially expressed in leaves and guard cells ), but also highly inducible by multi stress treatment such as drought, aba, high salinity and low temperature. quantitative analysis showed that gus activity in roots was very weak and no great changes were observed after treatment
通過對t1代轉基因苗的組織化學定位表明,該啟動子驅動的gus基因在逆境(如乾旱、 aba 、高鹽和冷)脅迫的葉片中表達,根中不表達,且老葉中的表達量高於幼葉中的表達量,說明其表達受發育階段的調控。There is a relationship between catenin phosphorylation, translocation and tumoregenesis, further more, in this relationship, cell signaling cascade and mitogen and their receptors are involved. base on these evidences, people are trying to disturb the key molecules in this signaling cascade for anti - tumor purpose
表皮生長因子( egf )能使p120 ~ ( ctn )酪氨酸磷酸化,磷酸化使bel - 7404細胞的粘附能力降低而遷移行為增強; p120 ~ ( ctn )在細胞內的分佈出現明顯的核內轉位, -連環蛋白也出現相似的變化。Cellular membrane is the possible action site for elf - emf, and the related studies confirmed that the receptors on cell membrane could be clustered by physical stress factor, and the receptors transduced the signal into cells via cellular signal pathway
細胞膜是電磁場信號的可能耦合位點,相關研究也證實了細胞膜受體在細胞轉導物理性應激因子中的作用。There is no characteristic in the amino acid sequence 63 - 152 and it is the piece that we want to delete to identify the function of the segment. ie180 gene mutants deleted the 64 - 151 amino acid was amplified by muti - pcr and were cloned by pmdist - vector. the clone plasmids were named pjmp1p3p2. the segment corresponding to the sequence of 1 - 1079 amino acid of the genbank sequence amplified by pcr, its clone plasmids was named pjmp1p2. the segment corresponding to the sequence of 454 - 1079 of genbank sequence amplified by pcr and its clone plasmids is named pjmp6p2 - three clone plasmids and pcdna3 were digested by restriction enzyme bamhi and hind, the gene segment of p1p2, p1p3p2, p6p2 were recycled
本試驗應用dnamis及prosis軟體分別對genbank中登記號為no352564的ie180序列進行了蛋白質序列分析,結果表明其1 - 34段氨基酸序列具有典型helix - turn - helix特徵序列,並且富含酸性氨基酸d及e ,是典型的dna識別序列;富含絲氨酸序列的152 - 409氨基酸序列是一個與激活有關的、潛在的磷酸化位點; 454 - 696氨基酸區域是dna結合域; 64 - 151氨基酸片段沒有明顯的序列特徵;從中可看出ie180蛋白的1 - 1080氨基酸段具有典型的轉錄激活因子結構特徵。Then introduce berry ' s work of finding phase factors including quantum phase factors accompanying adiabatic changes, on the base of this, discuss berry phase factors of spinl / 2 particle in rotating magnetic field
本文接著介紹了berry1984年發現幾何相因子的工作,內容包括從量子絕熱定理推導berry幾何相因子。在此基礎上,把旋轉磁場中自旋1 2系統作為研究對象,對其幾何相位的變化特點進行了討論。One of them was forecasted to produce transcript factor binding site in intron 6 of silky tyrp1. gel - shift result of this mutation proved that there is transcript factor binding site around the mutated site
經過預測,發現其中的一個snp可能使絲羽烏骨雞的內含子6中出現了新的轉錄因子的結合位點。The absorbed doses are obtained with a uniform state ion chamber that is formed with liftld cavity and lif wall and designed by ourselves. the key problem, the dose to fluence conversion factor of the photon with single energy from 0. 1 mev to 12mev, has been solved by simulating with monte carlo code system egs4
用m - c方法計算了固體電離室對0 . 1mev 12mev的單能光子的單位光子注量? lif吸收劑量的轉換因子,從而解決了由高能光子吸收劑量實測值轉換成光子注量時所面臨的困難問題。The analysis on the 5 " flanking region revealed tata box, putative api and nur77 response elements, prl and progesterone response elements motifs related with regulation on 20ahsd gene expression
通過軟體對克隆到的5側翼區結構和功能分析,發現了20 hsd基因的tatabox 、 prl反應元件、類固醇激素反應元件、 ap1和nur77等轉錄因子結合位點。In order to get some functional clues from their structures, the upstream regulation region of ndrgl gene and second structure of ndrg2 protein are performed bioinformatics analysis ; we found that there are several binding sequences of some diffirent transcription factors, their functions include regulating tissue - specific gene expression, regulating expression of genes related to growth and early development of cells, besides this, regulating expression of genes under some stimulated conditions, and so on. predict in protein fold classification shows that ndrg2 belongs to alpha / beta hydrolase fold family, and there are high similarity between ndrg2 and epoxide hydrolase from bacteria, this suggests that ndrg2 protein may has enzymatic functions associated with resisting the oxidative stress, maintaining the balance of cell redox potential, involving in the metabolism process of xenobiotics or intracellular toxic molecules
研究發現呷基因的調控區存在多種轉錄因子結合位點,功能主要涉及組織特異性表達調控,細胞生長發育相關基因的表達調控,刺激反應基因的表達調控等; ndrgz蛋白在結構上屬于a小水解酶類折疊,折疊分類預測表明ndrg2與其中的的細菌環氧化物水解酶的二級結構極為相似,提示ndrgz蛋白具有一定酶活性,可能參與細胞抗氧化應激反應,維持細, an ) armtbffiofbfochmilsyn ) mdafblechmrbfobo4第四軍醫大學碩士學位論文胞內氧還電勢平衡,參與內外源有毒物質的代謝等。A method of predicting human tumor peculiar promoter is introduced. by using transcriptional factor binding sites, this technique can receive a result well and truly
摘要本文介紹了一種利用轉錄因子結合位元點應用計算機技術對人類腫瘤特異性啟動子進行預測的方法。實驗結果證明該方法具有較高的準確性。Through bioinformatic analysis, we know that the pdipl gene was mapped to mouse chromosome 7 at f3. pdip1 may be a transcription factor functioning in the cell nucleus
通過生物信息學分析,我們得知小鼠pdip1基因位於7號染色體的f3位點上,可能是一個轉錄因子在細胞核內發揮生物功能。Completely analyze and discuss berry phase factors of spinl / 2 particle in rotating magnetic field. give the meanings of berry phase " geometrical description
全面分析和討論了在旋轉磁場中自旋1 2系統的berry相位因子,給出了berry相位的幾何詮釋。In this dissertation, jurkat cells, hela cells and mouse spleen t lymphocytes were chosen as experimental materials to answer the question. with the aid of various techniques such as elisa, immuno - co - precipitation, indirect immunofluoresent co - localization, double - labeling immunoelectron microscopy and so on, the relationships of baf complex with nf1 / ctf and rna polymerase ii were careful observed and analyzed
本文以jurkat細胞、 hela細胞和小鼠脾t淋巴細胞為研究材料,通過酶聯免疫吸附實驗( elisa ) 、免疫共沉澱、免疫熒光共定位和免疫電鏡雙標記等實驗,觀察和分析了baf復合物與轉錄因子nf1 ctf和rna聚合酶在基因轉錄活動中的相互聯系。Extension of low k + treatment to 12 hours did not increase the binding sites or protein abundance either. among ros species, h2o2 was specifically involved in the up - regulation of na, k - atpase induced by low k. 96 base pairs of upstream of na, k - atpase subunit promoter was the key cis - element in transcriptional regulation of promoter activity
Ros對鈉鉀atp酶亞基啟動子的刺激作用縮小至編碼區上游96堿基對,該序列包含多個潛在sp1轉錄因子結合位點,研究也表明sp1參與了低鉀對鈉鉀atp酶的調節作用。分享友人