誘導探針 的英文怎麼說

中文拼音 [yòudǎotànzhēn]
誘導探針 英文
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  • 誘 : 動詞1. （誘導） guide; lead; induce 2. （使用手段引人隨從自己的意願） lure; seduce; entice
  • 導 : 動詞1. （引導） lead; guide 2. （傳導） transmit; conduct 3. （開導） instruct; teach; give guidance to
  • 探 : Ⅰ動詞1 （試圖發現） try to find out; explore; sound 2 （看望） call on; visit; see 3 （向前伸出）...
  • 針 : Ⅰ名詞1 （縫衣物用的工具） needle 2 （細長像針的東西） needle like things 3 （針劑） injection; sh...
  • 誘導 : guide; lead; induce; guidance; induction
  • 探針 : probe; sound; filling fork; feeler; explorer; probing pin; touch needle; wire probe
  1. Our previous studies showed existence of apoplast cam in the plant cell and cam had many extracellular functions. so it supposed cam may be one of important extracellular polypeptides and trigger the intracellular signal transduction by binding the receptor. in this study, radiolabelled ligand is used to investigate the binding characteristic of cam and a. thaliana protoplasts. and chemical crosslinking is employed to explore binding proteins in the membrane. at first, ( 35 ) ~ s - cam was produced using ( 35 ) ~ s - labeled amino acid mixture in e. coli. sds - page and autoradiograph indicated high - purified, high - specific radioactivity ( 35 ) ~ s - cam was obtained. electrophoresis of ( 35 ) ~ s - cam is the same as that of unlabeled cam with ca ~ ( 2 + ) or egta ; a quatitive of protoplasts was prepared by enzymolysis

    首先，用~ （ 35 ） s標記的氨基酸混合物喂養工程菌成功地制備了~ （ 35 ） s標記的擬南芥鈣調素（ ~ （ 35 ） s - cam ） ， ~ （ 35 ） s - cam純度高、放射活度高、 ca ~ （ 2 + ）與egta存在時的電泳行為與未標記cam相同，可作為一種高靈敏性的探針用於進行受體學分析實驗；用擬南芥種子誘導愈傷，通過酶解制備了大量原生質體。
  2. Aiming at the present design fashion of domestic bigger tunnel, simulating a bigger tunnel with catholic characteristic, confirming the parameters of traffic inducement and controlling ( tunnel length, traffic, the selection and location of detection equipments, amount of roadway indicative lamp, etc ) on the base of the analog tunnel, discussing the controlling and revulsive mode of tunnel. briefly discussing the constitution of tunnel surveillance and controlling system and the executive means of traffic controlling and inducement subsystem and network structure of tunnel controlling system. finally discussing the conformation of emulational tunnel ' s database and detailed executive program by programming the computer emulation of controlling induce subsystem

    論文圍繞「交通誘導與控制」這一中心展開，探討長大隧道交通誘導與控制設備及其控制誘導方式；結合國內外對交通流模型研究的成果，提出一套適合長大隧道交通流特點的交通流模型；並針對目前國內長大隧道的普遍設計方式，模擬一個帶有普遍性特徵的長大隧道，確定了關于交通誘導與控制方面的參數（隧道長度、交通量、檢測設備的選取和位置、車道指示燈的數目等） ；以此模擬隧道為基礎，進一步探討隧道的具體控制與誘導方式；簡要探討隧道監控系統的構成、交通控制與誘導子系統的實現方式，隧道控制系統的網路架構；最後通過編程實現控制與誘導子系統的計算機模擬，討論關于模擬隧道數據庫的構建，具體編程實現等。
  3. In order to study the expression of 3 - defensins in liver as acute phase response proteins, a murine systemic acute phase responsive model was established by intraperitoneal injection o f lipopolysaccharide ( lps ) in our study. the mbd3 cdna sequence ( 145 - 169 bp ) was labled with [ - 32p ] atp as a probe to detect mbd3 mrna in different tissues by northern blot and analyze the time - and dose - dependant expression caused by lps. the 5 " flanking sequence ( - 167 - 179 bp ) of the mbd3 gene was designed as the probe and labled with [ - 32p ] dctp to investigate the binding of transcriptional factors to this region by electrophoretic mobility shift assay ( emsa ) and south - western blot

    以小鼠mbd3基因145 ? 169bpcdna序列合成探針，經[ - ~ （ 32 ） p ] atp標記后通過northernblot方法檢測mbd3在肝臟中的表達，同時分析了mbd3基因誘導表達的組織特異性，劑效和時效關系；結合mbd3基因啟動子區序列分析，以- 164 ? - 179bp雙鏈dna序列合成探針，經[ - ~ （ 32 ） p ] dctp標記后通過電泳遷移率改變實驗（ emsa ）和south ? westernblot方法對參與mbd3在肝臟中誘導表達調節的轉錄因子進行分析。
  4. Measurement of cell calcium ( review ) methods for the intracellular ca2 + measurement such as aequorin, metallochromic indicators, ion - selective electrodes and fluorescent ca2 + indicators, particularly the fluorescent ca2 + indicators were reviewed in detail. 2. synthesis of new fluorescence ca2 + indicators and study on their properties tow new fluorescent ca2 + indicators stdin and stdbt have been designed and synthesized and their structures, spectral and biological properties have been studied thoroughly

    2 . 5一ht誘導胃底平滑肌細胞鈣火花的研究以合成的胞漿特異性caz +熒光探針stdhi一am標記細胞，採用激光共聚焦線掃描技術，首次觀察到5一ht誘導胃底平滑肌細胞胞內鈣釋放的最基本單位一一j塑必嘗華盆翔望嘗『一盈些沁（ elementaryevents ） ， 「鈣火花（ ealeiumsparks ） 」現象。
  5. Changes in h2o2 generation in guard cells of vicia faba induced by aba were measured by using fluorescence probe, 8 - hydroxypyrene - l, 3, 6 - trisulfonic acid ( hpts ). examination of epidermis peel was performed using a laser scanning confocal microscope ( lscm ) and spectrofluorometer, set to an excitation light of 405 nm and an emission light of 512 ran

    以蠶豆葉片下表皮為材料，將熒光探針hpts導入蠶豆氣孔保衛細胞內，利用熒光光譜和激光共聚焦顯微鏡技術，檢測了aba誘導蠶豆氣孔關閉過程中h2o2的產生。
  6. Based on epidermal strip bioassay, microinjection, patch - clamp and laser scanning confocal microscopy in the experiments, we provided the first evidence that map kinases, including mek1 / 2 or p38 / hog1, plays an important role i n aba - or sa - induced h2o2 signal initial, amplification and specific targeting in response to stimuli in guard cells. aba - or h2o2 - induced vicia faba stomatal closure. was inhibited or reversed by the specific inhibitor pd98059 of mek1 / 2 ; the guard cells were pre - incubated or - microinjected by 10 umol l - 1 pd98059, aba could not enhance the fluorescence intensity of h2o2 probe dichlorofluorescein ( dcf )

    在對照實驗中， aba誘導熒光迅速增高；單獨的pd98059 、 pd98059和aba共同處理氣孔時，保衛細胞內h _ 2o _ 2探針熒光強度沒有增高；將pd98059注射進入其中的一個保衛細胞，再以aba處理，使得兩個有同樣熒光基礎的保衛細胞熒光強度對比強烈；將pd98059顯微注射進入已被aba誘導dcf （ dichlorofluorescin ）熒光強度升高的氣孔保衛細胞，熒光強度下降，而沒有被注射一邊的保衛細胞中的dcf熒光強度不變。
  7. Most interestingly, on the contrary to aba, the dcf fluorescence intensity of guard cells treated by 100 umol l - 1 salicylic acid ( sa ) was not down - regulated by pd98059, yet pd98059 did not regulate the stomatal movement being induced by light, dark or salicylic acid

    但是， pd98059和sa共同處理， hzoz探針熒光強度升高; sa誘導dcf熒光強度升高后，以pd98059處理，對dcf熒光強度無影響;將pd98059注射進入其中的一個保衛細胞，以sa處理，結果顯示兩個細胞內的熒光強度一樣。
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