電泳顯示 的英文怎麼說

中文拼音 [diànyǒngxiǎnshì]
電泳顯示 英文
electrophonic display
  • 電 : Ⅰ名詞1 （有電荷存在和電荷變化的現象） electricity 2 （電報） telegram; cable Ⅱ動詞1 （觸電） give...
  • 泳 : 動詞（游泳） swim
  • 顯 : Ⅰ形容詞1 （明顯） apparent; obvious; noticeable; evident 2 （有名聲有權勢的） illustrious and inf...
  • 示 : Ⅰ動詞（擺出或指出使人知道; 表明） show; indicate; signify; instruct; notify Ⅱ名詞1 [書面語] （給...
  • 顯示 : 1 （明顯地表示） show; display; demonstrate; exhibit; evince; manifest; discover; reveal; vision ...
  1. ( 2 ) the mortality of cp cell in 10 were increasing directly related with the time in the low temperature. after 120d some cp cells died in the way of apoptosis. most nucleus of cells were condensed, and chromosome was marginated beside the nucleus inner membrane, cell sizes were reduced, dna ladder showed in dna gel electrophoresis

    （ 2 ） cp細胞系在10低溫下細胞死亡率與時間成正比， 120d的細胞具典型的凋亡現象，即細胞核固縮、染色體邊集在核膜內側；細胞體積變小；瓊脂糖凝膠電泳上顯示特徵性的「梯狀」帶。
  2. The result shows that mms can induce dna - damage of yeast cells and the situation of dna - damage aggravated with increase of mms concentration

    結果顯示mms能夠引起酵母細胞dna的損傷，並且隨著mms濃度的增加dna損傷程度加重， 0 . 5 %瓊脂糖凝膠電泳及eb染色顯示1 ~ 。
  3. The peroxidase activity of variant t220x was obviously higher than acceptor lu22 at seedling stage. the result of peroxidase electrophoresis indicated that there were difference both in the depth and in the amount of zymogram between lu22 and t220x. so it was concluded that the variety of peroxidase was the result of change of heriditary substance

    小麥幼苗期過氧化物酶活性的測定顯示，變異體t220x的酶活性高於受體魯22 ；過氧化物酶電泳顯示， t220x和魯22過氧化物酶在酶帶深淺和數目方面都存在差異，說明外源遺傳物質已影響到過氧化物酶的變化。
  4. There were some degration in the purified protein, but gst - ap - 2 a still had the dna binding activity in the gel shift assay. the gst - testin and gst - antn1 were used for immunolize rabbits

    雖然所提取的融合蛋白gst - ap - 2出現較多降解，但是電泳遷移率變動分析顯示其仍然具有良好的dna結合活性。
  5. After the recombinant plasmid pcdna3. 1 / ts87 was identified by digestion of hindlll and bamh i, it transformed into cos7 by lipofectamine. expression product was identified by immunohistochemical method, sds - page and western - blot. the immunocytochemistry result has shown that specific brown - staining grains were found in the cytoplasm of cells transformed by recombinant plasmid versus not seen in cells transformed by pcdna3. 1 or normal cells ; the sds - page result has revealed that a band about 3 8kb was found in cell lysis transformed by recombinant plasmid versus not in cells transformed by pcdnas. l or normal cells ; the western - blot result has showed that only the band about 38kd was recognized by sera from rabbit infected by t. s artificially and sera from rabbit immunized with soluble antigen of t. s and with protein expressed by ts87 gene and by a monoclonal antibody of t. s

    通過細胞的免疫組化，細胞裂解物的sds - page電泳， westem - blot分析檢測目的基因的表達情況。免疫組化結果顯示：重組質粒轉染的細胞質中有棕褐色顆粒，而空載體轉染細胞及正常細胞無此現象；細胞裂解物sds - page電泳結果顯示：只有重組質粒轉染的細胞在約38kd處有明顯的蛋白帶，這與理論計算的ts87基因表達蛋白的分子量為38kd基本一致； western - blot分析結果顯示：約38kd的蛋白帶能夠分別被旋毛蟲感染兔血清，成蟲蟲體可溶性抗原免疫兔血清， ts87基因原核表達蛋白免疫兔血清（ ts87血清）以及一株具保護性的旋毛蟲單抗特異識別。
  6. All of these indicated that arsenic trioxide was a powerful chemotherapeutic agent and the cells in the treatment group were induced to apoptosis. to further understand the molecular mechanisms of arsenic trioxide treatment in the induced cellular apoptosis, we applied the restriction display - pcr ( rd - pcr ) technique combined with polyacrylamide gel electrophoresis and sliver staining techniques to separate the differentially expressed genes

    為了進一步闡述as _ 2o _ 3作用的分子生物學機制，我們首先應用rd - pcr技術，結合聚丙烯酰胺凝膠電泳和銀染技術分離和顯示了as _ 2o _ 3作用k562細胞前後的cdna片段，發現了11個差異表達的基因片段。
  7. Isozymes in different tissues of three stains of crucian carp were studied comparatively. the results indicated that pengze crucian carp is different from silver crucian carp in biochemical level, they probably came from different region. the electrophoretogram of pengze crucian carp and silver crucian carp all included the basal patterns of wild crucian carp

    通過對三種鯽魚品系不同組織同工酶的電泳圖譜的比較研究，揭示了彭澤鯽和銀鯽至少在生化水平上已有明顯的分化，很可能起源於不同的地區，獨立演化而形成。
  8. The mechanisms of such treatment have been proposed as inhibition of proliferation and angiogenesis, as well as induction of differentiation and apoptosis, as has been tested by various in vivo and in vitro experiments. in our experiments, it has also been demonstrated that after the treatment of arsenic trioxide, the k562 cells has undergone major morphological changes, which included nuclear shrinkage, membrane bleb and scattered apoptotic bodies. dna gel electrophoresis also discovered that the typical " dna ladder " phenomena in the treatment group, while the control group showed the regular genomic banding

    我們在實驗中觀察到as _ 2o _ 3作用人紅白血病k562細胞后，細胞生長明顯變緩，部分細胞出現皺縮、染色質濃聚及胞膜起泡現象，部分細胞胞膜破裂，在其周圍有緻密的凋亡小體出現， dna電泳出現典型的凋亡「梯狀」帶，提示as _ 2o _ 3能有效抑制k562細胞生長，誘導k562細胞凋亡。
  9. In this article, we microinjected camp ( as activator of pka ) and protein kinase inhibitor ( pki ) ( as inhibitor of pka ) into mouse 1 - cell stage fertilized eggs, the camp concentration, pka and mpf activaty were detected, also the cdc25c, cdc2 phosphorylated state and the concentration of ptyr15 for cdc2, cyclin b1. materials females of 4 - 5 week - old kuming mice and males of 8 week - old kuming mice were supplied from the department of laboratory animals, china medical university

    本實驗應用pka激動劑camp及抑制劑pki顯微注射入小鼠二一細胞期受精卵並觀察卵細胞m期形態學變化及pka對mpf活性的影響以及cdc25c ， cdcz電泳遷移率， cdcz的磷酸酪氨酸ptyrl及周期素b含量，為揭示pka在哺乳動物細胞周期調控機制，對生長、發育、癌變、死亡的研究提供理論依據。
  10. Materials and methods in our study, first the e. coli bl21 transformed already are cultivated in smaller scale and then the plasmids dna were extracted by the methods of alkaline lysis. the plasmids dna extraction were processed 37 overnight by the restrictive endo - incisase bam h i and xho i. the incision products were used to check the integrality and variability of the recombinant plasmids dna by 1 % agarose gel elec - trophoresis

    同預想結果基本吻合，大規模培養后純化得到的融合蛋白通過sds page顯示在52kda處有一條帶，而酶切后產物電泳結果顯示在26kda處分另有兩條蛋白帶，其中一條為gst ，另一條為hbrp ，基本符合實驗結果； hbrp對tpk活性的抑制呈劑量依賴性。
  11. Cells were then harvested by centrifugation and the pellet was resuspended in phosphate - buffered saline ( pbs ) containing 5 mm edta. after sonication, debris was removed by centrifugation at 10000 x g for 15 min at 4

    挑取轉化后的大腸桿菌提取質粒， ecori和hindln酶切質粒進行鑒定，瓊脂搪電泳顯示含有大約800kb的目的片段。
  12. The results from sds - page presented that there were three female specific protein subunits with molecular weights of 123 kd, 120 kd and 91 kd, respectively. we can conclude the higher molecular compose of two subunits ; the results from two dimension electrophoresis showed the isoelectric points of two female - specific spots with molecular weight of about 120kd were 5. 5 and 5. 7. immunodiffusion reactions demonstrated that vg existed both in female fat body and hemolymph, which as vn was deposited in the ovary, while not in the male

    Page電泳結果表明：麗蠅蛹集金小蜂明顯存在2條雌特異性帶-卵黃蛋白，分子量分別為181kd和136kd ； sds - page電泳分析：存在3條雌特異性帶，其分子量為123kd 、 120kd和91kd ，由此，可推定卵黃原蛋白（ vitellogenin ， vg ）和卵黃磷蛋白（ vitellin ， vn ）由2個蛋白組成，其中分子量較大的蛋白由2個亞基組成；雙向電泳結果顯示，在120kd附近有兩個特異性點，其等電點為5 . 5和5 . 7 ；雙擴散表明，麗蠅蛹集金小蜂卵黃磷蛋白的抗血清與雌隱成蟲蟲體、脂肪體、血淋巴和卵巢勻漿液均有免疫沉澱反應，而與雄蜂血淋巴無免疫反應，說明了vg與vn具有免疫同源性，是雌特異性蛋白，且由脂肪體合成。
  13. The results showed that the electrophoric patterns of isozymes of " allogynogenetic crucian carp " were the same as those of its female parent and significantly different from its male parent

    結果顯示：異育淇鯽同工酶的電泳圖譜與母本淇鯽相同，與父本興國紅鯉顯著不同。
  14. One 66kd band appeared except 44kd main band when go isozyme above was subjected to sds - page and ce - sds, indicating this go isozyme was similar to that from spinach leaves which contained 40kd and 66kd simultaneously. whether b - mercaptoethanol was added or not when go isozyme was subjected to in sds - page and ce - sds, 40kd main band and 66kd band still appeared, indicating two subunits were not linked by covalent disulfide. amino acid analysis shew that the ratios of basic to acidic amino acid of go isozyme and its 40kd acidic subunit were 0

    菜心go同工酶的sds - page和sds -毛細管電泳（ ce - sds ）顯示，該酶除了含40kd主帶外，還有很淺的66kd帶，和之前我們提出的菠菜go同工酶含40kd酸性亞基和66kd堿性亞基相似； sos - page和ce - sds電泳中，無論加入-巰基乙醇與否， go同工酶都只有40kd主帶和66kd淺帶，表明菜心go同工酶中40kd酸性亞基和66kd堿性亞基不是以共價二硫鍵相連；用制備性sds - page法獲得菜心go同工酶的40kd亞基，並和菜心go同工酶一起測定其氨基酸組成，該go同工酶及40kd亞基的堿酸性氨基酸的比例分別為0 . 66和0 . 54 ，表明40kd亞基可能是個酸性蛋白，而66kd帶則是個堿性蛋白。
  15. In this study, the profiles of proteins expesssion in different growth phases of rt19 have been obtained using the technique of proteome analysis with two - dimensional polyacrylamide gel electrophoresis ( 2 - d page ). an efficient imagemaster 2d was used to reveal the number of protein spots corresponding from lag phase to stationary phase, varying from 398 to 516, which manifested kinetic state of proteome in cell

    本文採用高解析度的雙向電泳技術，得到不同生長時期的蛋白表達譜，應用高效的imagemaster2d軟體進行圖譜分析，結果顯示： （ 1 ）從延滯期到穩定期的末期，所表達的蛋白數量由398個逐漸增加至516個，顯示了細胞內的蛋白在不同生長期的動態表達水平。
  16. Gene had been highly expressed after incubating the transformed strains in the inducing culture

    基因已被轉化，誘導培養后的蛋白電泳顯示
  17. And we have also studied its expression in protoryotes and the conserved regions of insect chitinase genes in different insects pests

    Sds page電泳顯示，在50th附近沒有特異蛋白帶的出現，此結果表明外源基因沒有得到表達。
  18. This gene was inserted into expressing vector pgex - 4t - 1, which could express a gst fusion protein in e. coli. strain bl21 ( de3 ) by iptg inducing

    將己該基因構建到融合蛋白表達載體pgex - 4t - 1 ，通過iptg誘導，進行原核蛋白表達， sds - page電泳顯示，有約48kd融合蛋白表達。
  19. The lesions can be seen with mri scans, but the appearance in the csf of increased protein from igg that demonstrates oligoclonal bands on electrophoresis is very consistent with this diagnosis

    採用磁共振（ mri ）掃描可發現損害，腦脊液檢測結果為免疫球蛋白g升高，這表明電泳顯示的寡克隆帶與診斷是非常一致的。
  20. The examination of the urine specimens by gel chromatography and electrophoresis showed that the active ingredient excreted in the urine was partly unchanged and partly depolymerized to molecules of shorter chain lengths

    用凝膠電泳色譜法檢測尿液顯示，尿液中的活性藥物成分部分為原形，部分解聚成更短的分子鏈。
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