表達分析 的英文怎麼說

中文拼音 [biǎodáfēnxī]
表達分析 英文
transcript expression analysis
  • 表 : Ⅰ名詞1 （外面;外表） outside; surface; external 2 （中表親戚） the relationship between the child...
  • 達 : Ⅰ動詞1 （暢通） extend 2 （達到） reach; attain; amount to 3 （通曉; 明白） understand thoroughly...
  • 分 : 分Ⅰ名詞1. （成分） component 2. （職責和權利的限度） what is within one's duty or rights Ⅱ同 「份」Ⅲ動詞[書面語] （料想） judge
  • 析 : Ⅰ動詞1. （分開; 散開） divide; separate 2. （分析） analyse; dissect; resolve Ⅱ名詞（姓氏） a surname
  • 表達 : deliver; express; show; voice; convey; communicate
  1. A kind of new - style portable zxc air pump

    基因的克隆與表達分析
  2. Cloning and expression analysis of a new glutelin cdna in rice

    水稻穀蛋白的一個新基因克隆及表達分析
  3. Molecular cloning and expression of oscmo encoding a putative choline monooxygenase in rice oryza sativa l

    水稻膽堿單加氧酶基因的克隆與表達分析
  4. Molecular cloning and expression analysis of a serine threonine protein kinase gene in upland cotton

    蘇氨酸激酶蛋白基因的克隆與表達分析
  5. Isolation and rna expression pattem of a type 2 metallothionein - like gene in amaranthus cruentus l

    型金屬硫蛋白基因的分離及其表達分析
  6. Is encoded by grb ~ ast7. the expression analysis of the concatemer was proceeded in the e. coli pet expression system

    本文主要工作就是構建grb - ast _ 7串聯體，將構建后的串聯體導入大腸桿菌進行表達分析。
  7. Neuropeptide ast2 is encoded by grb - ast3. pcr methods were tried to construct grb - ast3 concatemer. the expression analysis of the concatemer was proceeded in the e. coli pet expression system

    本論文採用改進的pcr 「自身模板-引物」法進行構建方法構建grb - ast _ 3串聯體，並將拼接好的串聯體轉入大腸桿菌進行表達分析。
  8. Histological, immunohistochemical and gene expression analyses of endometriotic tissue proide detailed information on the angio - architecture of endometriotic lesions and the different growth factor expression by arious cell populations

    異位組織的組織學，免疫組化和基因表達分析為異位損傷的血管構造和不同細胞群表達的不同生長因子提供了詳細信息。
  9. Lrp15 gene promoter region methylation and its expression in acute leukemia

    15基因啟動子區甲基化及其表達分析
  10. Following researches verified that the cam - binding domain exists in the c - terminal of ecbp21

    通過缺失表達分析實驗證實cambd結構域位於ecbp21的羧基端。
  11. Expression analysis the expression analysis of gharf in different tissues of cotton was carried out by rna dot blotting with ghakf probe labeled with dig. the result showed that the expression of arf gene was mainly in anthers of sterile and fertile, pollen of fertile, corolla rather than in leaves, radicel and ovule

    棉花ari ； 』基因的表達分析用地高辛將棉花arf基因標記為探針，與棉花洞a的不育株花藥、司有株花藥、可育花粉粒、葉片、花冠、胚根和胚珠的總rna進行斑點雜交。
  12. Monitor and control pseudorabies in breeder pig farm of helongjiang province

    轉人血清白蛋白基因豬的表達分析
  13. Character analysis of a novel testis - specific tsc23 gene in mouse and human testis

    23在小鼠和人睪丸組織中的表達分析
  14. Expression of soluble intracellular adhesion molecule in peritoneal fluid in patients with endometriosis

    盆腔炎腹腔液中的表達分析
  15. With the advance of human genome project, bioinformatics has been promptly developed in recent 20 years. as a branch of a new class of bioinformatics which allows the monitoring of expression levels for thousands of genes and proteins simultaneously, biochip technologies are increasingly applied to broader fields

    隨著人類基因組計劃的提出與開展，生物信息學在近20年內得到了迅猛的發展，作為生物信息學領域一個新分支的生物晶元技術由於能夠同時對成千上萬的基因和蛋白質片斷進行表達分析，已經得到了越來越廣泛的應用。
  16. Once the recombinant virus has been i - dentified, we amplified the p - 1 stock to attain the large scale, high - titer viral stock in order to initiate expression studies. the recombinant angiostatin was produced from spodoptera frugiperda 9 ( sf9 ) insect cells infected by the high titer virus stock we have prepared. the time course for expression of recombinant protein was detected by sds - page and western blot, which can determine the optimal multiplicity of infection ( moi ) and the appropriate time of harvest for the protein

    表達重組蛋白angiostatin ：用制備好的帶有矗s標記的融合性angiostatin基因的高滴度重組桿狀病毒貯存液感染草地貪夜蛾sfg細胞，用sds page電泳和hsternblot對感染不同時間後分泌的重組蛋白做時間表達分析，依此確定最適的感染復數（ moi ）和感染時間，以達到重組蛋白表達水平最適化，而後大規模進行重組蛋白的表達， sds page用來分析重組蛋白， westernblot用來在蛋白表達水平低的情況下檢測表達的特異重組蛋白。
  17. These results showed that hsp70 is highly conserved in shrimps. semi - quantitative rt - pcr was developed to study the hsp70 transcription pattern in fenneropenaeus chinensis. the transcription of hsp70 was detected in the major tissues of hepatopancreas, muscles, eyestalks under both normal and heat shocked conditions. the mrna level was increased after the animals were heat shocked in the 3 tissues

    為了研究中國對蝦hsp70的轉錄表達，發展了半定量rt - pcr方法，對hsp70轉錄表達分析顯示， hsp70mrna在中國對蝦正常肝胰腺、肌肉、眼柄組織存在組成性表達；在受到整體熱休克后的對蝦肌肉、肝胰腺、眼柄組織hsp70轉錄水平增加。
  18. Third, we examined the expression of ecbp21 dynamics during the incubation of angelica suspension - cultured cells and stress treatments through northern blot analysis. during the incubation of angelica suspension - cultured cells, the expression of ecbp21 gene increased from 0 to 12th day, and it reached a peak on the twelfth day. while the expression of cam gene increased from 0 to 9th day, and it reached a peak during the 6th - 9th day

    3 . ecbp21表達分析: northernblot分析表明:在白芷懸浮培養細胞生長周期中， ecbp21和cam都為組成型表達， 0一12天ecbp21表達量逐漸增加，第12天達到最高，隨后12一21天， ecbp21表達量稍有下降，維持在一個比較穩定狀態;而o一6天時， cam表達量逐漸上升，第6一9天達到最大表達量，隨后， 9一21天， cam表達量有所下降。
  19. To study the biological function of sh2a gene, we constructed its recombinant expression vec - tor, and investigated its function by cell transfection, kinase assay, subcellular localization and expression analysis. materials and methods 1

    我們構建了sh _ 2a基因的真核重組表達載體，通過細胞轉染、激酶活性檢測、亞細胞定位、表達分析和流式細胞儀等方法對其功能進行了初步的研究。
  20. The scfv genes were then inserted into the prokaryotic fusion protein expression vector ptat - ha and expressed in e. coli bl21. after the expression products were purified by ni - nta colume, their activities were analysed

    將獲得的不含前導肽的單鏈抗體基因克隆入ha和6his融合的原核表達載體ptat - ha ，在大腸桿菌bl21中進行表達，分析其表達情況。
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