綠色熒光蛋白 的英文怎麼說

中文拼音 [shǎiyíngguāngdànbái]
綠色熒光蛋白 英文
egfp
  • : 綠形容詞(像草和樹葉茂盛時的顏色) green
  • : 色名詞[口語] (顏色) colour
  • : 形容詞[書面語]1. (光亮微弱的樣子) glimmering 2. (眼光迷亂; 疑惑) dazzled; perplexed
  • : Ⅰ名詞1 (照耀在物體上、使人能看見物體的一種物質) light; ray 2 (景物) scenery 3 (光彩; 榮譽) ...
  • : 名詞1. (鳥類或龜、蛇類所產的卵) egg 2. (像蛋形的東西) an egg-shaped thing 3. (辱罵之詞)
  • : Ⅰ形容詞1 (似雪的顏色) white 2 (清楚; 明白; 弄明白) clear 3 (空的; 沒加他物的) pure; clear; ...
  • 綠色 : green綠色長城 green great wall; 綠色食品 food to be no pollution and best before; green food; 綠...
  • 蛋白 : 1. (卵中透明的膠狀物質) egg white; albumen; gary2. [生物化學] (蛋白質) protein
  1. First, to construct a recombinant plasmid pegfp - c - fos with c - fos promoter and egfp, and then transfect it into human bladder transitional cell carcinoma biu - 87 cell ; second, based on the changes of the expression of gfp in the biu - 87 cell which induced by the aconitine and hab toxins, the concentration of the hab toxins could be detected

    目的:構建一個含c - fos啟動子和egfp報告基因的pegfp - c - fos重組質粒載體。體外轉染膀胱癌biu - 87細胞后,利用赤潮毒素作用后細胞表達綠色熒光蛋白的變化來檢測赤潮毒素,初步建立一種以細胞為基礎受體水平的赤潮毒素檢測方法。
  2. Green fluorescent protein ( gfp ) gene was conjugated to the 3 " end of the pap gene in order to screen easily of the transgenic cotton plants. the combined gene was cloned into plant expression vector pbi121 and then transformed. about 5000 seeds of the transgenic cotton were obtained and the some seedlings of the transgenic cotton could give a bright green fluorescence in the dark condition when the cotton seedlings were irradiated with ultraviolet rays

    為了便於轉基因棉花後代的篩選,在pap基因的3 』端融入了綠色熒光蛋白gfp )基因,然後將融合基因克隆在植物表達載體pbi121上,再進行遺傳轉化,得轉基因棉花種子5000餘粒,將種子播種長到于葉展開時,先在黑暗中用紫外燈照射,查找表現的幼苗,然後再用地高辛( dig )標記的pap基因特異性探針對這些棉花進行點雜交,最後發現有8株棉花表現陽性反應,說明pap基因的確己經轉到了棉花的基因組中,其棉花黃萎病的抗性鑒定正在進行之中。
  3. It was confirmed by restriction enzyme digestion analysis that egfp fusion expression plasmids of scfvs were successfully constructed

    的序列正確,經酶切鑒定證實成功地構建了綠色熒光蛋白基因融合表達載體。
  4. Furtherly expression phase analysis showed that orf2 appeared in different form during infection. to reveal the function of haorf2, vha - orf2 - gfp recombinant virus which tagged with egfp - orf2 fusion protein was generated

    構建了ha2與綠色熒光蛋白融合表達的重組病毒vha - orf2 - gfp ,對該重組病毒感染細胞后,融合篡碩士學位論文mast卜r 』 s 』 r拼ifs
  5. We fused the gfp into the c - terminal region as well as n - terminal region of emt - 1 protein. the result showed that the localization of the protein encoded by the full length emt - 1 cdna was in endoplastic reticulum ( er ). extracellular region, transmembrane and intracellular region showed the similar cellular localization

    我們用綠色熒光蛋白融合於emt l全長及其不同截斷形式的梭基和氨基端,瞬時轉染cos 7細胞,通過顯微鏡觀察,發現emt l編碼的呈現內質網定位的特點。
  6. Green fluorescent protein gfp

    綠色熒光蛋白
  7. Improvement of genetic transformation system by using gfp as reporter gene on pepper

    應用綠色熒光蛋白報告基因優化辣椒的遺傳轉化體系
  8. Construction of recombinant adeno - associated virus vector expressing glial cell line - derived neurotrophic factor labeled by green fluorescent protein

    綠色熒光蛋白標記的大鼠膠質細胞源性神經營養因子重組腺病毒載體的構建及其表達
  9. The application of green fluorescent protein in plant

    綠色熒光蛋白在植物細胞生物學中的應用
  10. Application of green fluorescent protein labeling in the study of stem cells transplantation

    綠色熒光蛋白標記在幹細胞移植中的應用
  11. As a report probe, the green fluorescent protein ( gfp ) had been broadly employed in research works

    綠色熒光蛋白( gfp )作為報告探針,已經在研究工作中廣泛地應用。
  12. Production of transgenic embryos expressing green fluorescent protein by nuclear transfer from different types of somatic cells in pig

    不同類型的轉基因細胞為核供體生產豬的轉綠色熒光蛋白基因克隆胚胎
  13. An unusual rice calmodulin isoform, oscam61, was first obtained in our lab, which contains an n - terminal cam domain and a c - terminal basic extension with a potential prenylation site. in vitro activity assays confirm oscam61 as a functional calmodulin. using the green fluorescent protein ( gfp ) as a visual marker, we further studied subcellular localization of oscam61 in stably transformed tobacco cells

    利用綠色熒光蛋白( greenfluorescentprotein , gfp )作為標記,研究了oscam61在煙草細胞中的定位, gfp - oscam61融合(具有開放的異戊烯化修飾位點)定位於細胞質膜和細胞器膜上,而oscam61 - gfp (異戊烯化修飾位點被gfp封閉)定位於細胞核的核質中。
  14. The symbiosis between mesorhizobium huakuii and astragalus sinicus is a chinese - characteristic symbiotic nitrogen fixation system, while molecular genetic study on its early symbiotic interaction is still at primary stage

    本文對新型報告基因?綠色熒光蛋白基因在華癸中生根瘤菌-紫雲英共生固氮體系早期結瘤階段分子遺傳學中的應用進行了探索性研究。
  15. Green fluorescent protein is widely applied in researches of modern life science, such as gene product moved - process in vivo, protein localization, drug screening and preliminary selection of transgenic individual as a molecular marker

    綠色熒光蛋白這種獨特的生物學特性,使其作為報道基因在現代生命科學研究領域中,如細胞內基因產物的動態過程,質在細胞內的定位,藥物的篩選,以及轉基因個體的初步鑒定等等有著廣泛的應用。
  16. Green fluorescent protein ( gfp ) was extracted from jellyfish ( aequerea victoria ) of ocean invertebrate. gfp can emit green fluorescent when it is illuminated by light of suitable wavelength. the emissions of fluorescence need not any additional factors, such as substrate, supplementary factor

    綠色熒光蛋白( greenfluorescentprotein , gfp )是來源於多管水母( aequoreavictoria )等海洋無脊椎動物的一種質,該質在體外經適當波長的激發便發出,並且這種的發射不需要任何底物和輔助因子的誘導。
  17. Improvement of adcmv - gfp gene transfection efficiency induced by heavy - ion beam irradiation on murine melanoma cells

    離子束輻射對用帶有綠色熒光蛋白基因的缺陷性腺病毒
  18. Based on the foundation research of the interaction of virus and host actin, we recombine gfp gene - a reporter gene - with 5c actin gene of drosophila melanogaster, a gfp - actin fusion gene was obtained

    本文在總結前人關于病毒與宿主肌動相互作用的研究的基礎上,利用綠色熒光蛋白基因為標記基因,與果蠅肌動基因5cactin基因融合,構成gfp - actin融合基因。
  19. 2. expression of gfp gene in b. thuringiensis strain green fluorescent protein gene is a very useful report gene which could be detected easily. it can be used in the detection of b. thuringiensis environmental release and study of the insecticidal mechanism

    綠色熒光蛋白基因在蘇雲金芽胞桿菌中的表達綠色熒光蛋白基因是一種容易檢測的報告基因,可用於蘇雲金芽胞桿菌制劑施用后的環境監測,殺蟲機理等方面的研究。
  20. In the research of transgenic fish, green fluorescent protein gene was sub - cloned to downstream of carp p - actin gene promoter that was cloned in pucusa by molecular recombination technology. thus pagfp plasmid was constructed successfully. the recombination was determined by digestion of restriction enzyme and sequencing

    實驗通過分子重組技術,採用定向克隆法將綠色熒光蛋白基因亞克隆到puc118a上鯉魚-肌動基因啟動子下游,構建成能在真核生物體內表達的表達載體pagfp ,經雙酶酶切法序列鑒定后,回收帶啟動子和目的基因片段。
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