flanking region 中文意思是什麼

flanking region 解釋
側翼區，旁側區
  • flanking : 側面攻擊
  • region : n. 1. 地方，地域，地帶；地區；行政區，管轄區，區；左近，鄰近；（大氣、海水等的）層，界，境。2. 【解剖學；動物學】（身體的）局部，部位。3. （學問等的）范圍，領域。4. 〈罕用語〉天空。
  1. Molecular cloning of 5 ' flanking region of ovine keratin associated protein 6 - 1 gene and comparison of the sequences

    端調控區的分子克隆及測序結果比較
  2. ( 3 ) at post - translation level plant mutual sequence of starting translation aaca and eukaryotic secretory signal peptide sequence was added to 5 ' - flanking region of t - pa gene and kdel ( sequence located to endoplastic reticulum ) to 3 ' - flanking region by pcr amplication and plant expression vector pbemt was constructed

    （ 3 ）翻譯后水平通過pcr擴增的方式在t - pa基因5端添加了真核分泌信號肽序列和植物翻譯起始共有序列aaca ，在3端添加了內質網定位序列kdel ，構建了植物表達載體pbemt 。
  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. Article 22 in a water - eroded region, by taking a small river basin comprising the natural ravines and flanking hill slopes as a unit, a comprehensive system for the prevention and control of soil erosion shall be set up on the basis of overall planning and comprehensive rehabilitation

    第二十二條在水力侵蝕地區，應當以天然溝壑及其兩側山坡地形成的小流域為單元，實行全面規劃，綜合治理，建立水土流失綜合防治體系。
  5. These results demonstrated the acbadh promoter is a strong salt - stress - induced promoter. the acbadh 5 ' - flanking region contains two salt - responsive enhancer regions localized between - 1114 and - 892, - 464 and - 234 and one sliencer region localized between - 892 and - 643

    對轉基因煙草的gus活性分析表明，在1114和892之間， 464和234之間存在增強子元件，而在892和643之間存在負調控元件。
  6. 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。
  7. Using transfac 4. 0 and tssg tssh nsite of softbeny, we can see that a tata box lie in - 188bp - 198bp from transcriptional initiation site, there are several api, c / ebp binding motifs near it or in other 5 " flanking region, a c - fos response element is in - 1133bp - 1143bp from transcriptional initiation site

    0軟體和softbeny網站上tssg ， tssh ， nsi 』 fe軟體共同分析，在a ? ibgp轉錄起始點上游j到一198區域存在tata盒，在其附近及其5 』上游遠端調節區存在多個api ， c ebp結合位點，並且在轉錄起始點上遊人到一處存在一個c fos結合基序。
  8. The aim of this part is that using bovine as1 - casein 5 ' regulation region and 3 ' flanking region to construct mammary gland expressing vectors

    本實驗旨在利用牛s1 ?酪蛋白的5 』調控區和3 』側翼區來構建乳腺特異表達載體。
  9. The research work was divided into 3 parts in this thesis : 1 ) 2. 5kb 5 " flanking region of the 20ohsd gene was isolated by pcr

    本研究工作主要分以下三個部分：第一部分運用pcr技術從大鼠promoterfinder文庫中擴增到了2 . 5kb的20 hsd基因5側翼區序列，並對其進行了序列測定。
  10. In this study, using bioscien tomato as test material and the flanking region of the bioscien insert sequence was determined using inverse pcr and real - time pcr. by means of verification, this sequence is specific for the transfection event

    本研究以華番1號為試材，利用反向pcr和熒光pcr技術已成功將華番1號轉基因整合位點dna序列擴增出來。
  11. Firstly, the bovine as1 - casein 5 ' regulation region was cloned into the vector pegfp - 1 and constructed a new vector p - 5 ; then the bovine asi - casein 3 ' flanking region was inserted into the position of gfp gene in the vector of p - s and a mammary gland universal expressing vector pbcas was created

    首先將牛s1 ?酪蛋白的5 』調控區克隆到載體pegfp - 1上，成為載體p - 5 ；然後將牛s1 ?酪蛋白的3 』側翼區克隆到載體p - 5的gfp基因位置，從而構建成乳腺通用表達載體pbcas 。
  12. Secondly, the chicken r - ifn cdna was introduced into the vector pbcas between the bovine asi - casein 5 ' regulation region and 3 ' flanking region to create a vector pbcasifn to examine if this bovine asi - casein 5 ' regulation region and 3 ' flanking region could regulate chicken y - ifn to express in the latex by producting transgenic mice

    最後，我們將雞?干擾素cdna插入到載體pbcas的牛s1 ?酪蛋白的5 』調控區和3 』側翼區之間，構建成載體pbcasifn ，以便於通過生產轉基因小鼠來檢驗牛s1 ?酪蛋白的5 』調控區和3 』側翼區是否可以調控外源基因雞?干擾素在乳腺中特異表達。
  13. Infectious bursal disease virus has been a great concern for the poultry industry for a long time, particularly for the past decade when its " re - emergence " in variant or highly virulent forms. in this study, two sets of primers ( pta and pts, ibda and ibds ), flanking the hyper - variable region of vp2 gene, were designed to run a reverse transcription polymerase chain reaction ( primary rt - pcr ) and nested - pcr. both of these assays can amplify all of 12 reference strains which including pathotypes cibdv, vvibdv and vibdv, but not the 5 negative reference pathogens of chicken

    結果12個參考毒株均能擴增出約679bp的目的片段，而陰性對照的常見5種雞病病原：雞新城疫病毒（ ndv ） 、雞傳染性支氣管炎病毒（ ibv ） 、雞傳染性貧血病毒（ caiv ） 、大腸桿菌和多殺性巴氏桿菌均沒有擴增到任何片段；應用建立的技術對疑似ibd的34份臨床病料進行檢測，並同時在基礎rt - pcr擴增的片段內設計另一對引物進行nested - pcr 。
分享友人
分享到 Line

分享到臉書