box gene 中文意思是什麼

box gene 解釋
盒基因
  • box : n 1 箱，櫃，匣，盒；罩殼；錢櫃；〈美口〉保險箱；郵箱，信箱；〈英國〉禮盒；禮物（旅行用）衣箱。2 ...
  • gene : n. 【生物學】基因。 dominant gene顯性基因。
  1. Cloning of a partial mads - box gene in groundnut arachis hypogaea l

    3基因編碼區的克隆與序列分析
  2. Using a pair of degenerate primers based on the conservative region, hmg - box, of human sry gene, tow different fragments of sox gene, essox3 and essox22 were amplified from female and male eriocheir sinensis, the sequence results indicated that essox3 and essox22 shown high homology to human sox genes, and the identities to human sox genes in dna sequence and amino acid sequence are 84 % 、 85 % and 97 % 、 81 %, respectively. it might be concluded that sox gene was highly conservative in phylogenesis

    二、研究論文1 、參照人sry基因hmg - box保守區的序列，設計一對兼并引物， pcr擴增了中華絨螯蟹的sox基因，並對擴增產物進行了克隆和測序。結果在雌雄個體中篩選出兩個不同的sox基因essox3和essox22 ，其dna序列和編碼的氨基酸序列與人相應sox基因的相似性分別為84 % 、 85 %和97 % 、 81 % ，顯示該基因在進化上具高度的保守性。
  3. The individuals of rhd - positive phenotype with intact exons carried generally insert fragments and boxl box2 and box3 and this proved that inserts or rh box could n ' t affect the express of rh d gene. in 2 of the 5 wei nationality pedigrees whose proband were rh d - negative, rhc / e phenotype of all the rh negative individuals was ccee. rhd exon 4nsert and rh box did not be found in all individuals

    在7個先證者為rhd陰性的漢族家系中，大部分成員均出現插入片段和rhbox ，且在遺傳上符合孟德爾遺傳定律， d外顯子完整且表型為rhd陽性的家系個體成員廣泛帶有插入片段和box1 、 box2或box3 ，插入片段或rhbox並未影響d基因的表達。
  4. To study on structure and inheritance of rh d gene interaction between gene expression of rh d and rh c / e and influences on rh d gene expression of inserts and rh box - methods : 20 pairs of oligonucleotide specific primers for exon, intron 2 4, insert and rh box of rh d, rhc / e gene were designed and composed the polymerase chain reaction - sequence specific oligonucleotide primer ( pcr - ssp ) was used to amplify the rh c / e gene, rh d gene, exon, intron, insert and rh box in 106 samples of unrelated individuals and 7 han nationality ancestries and 5 wei nationality ancestries whose proband were rh d - negative

    目的：觀察中國漢族非血緣關系隨機個體、漢族及維吾爾族家系rh血型的c e基因、 d基因外顯子、內含子、插入片段以及rhbox ，研究rhd基因結構及遺傳規律， d基因表達與c e基因的關聯，以及插入片段和rhbox對d基因表達的影響。
  5. Part two : studies l. the sox gene of rana rugulosa wiegmann was amplified by using the technique of pcr with a pair of primers which specially amplify the conserved motif ( hmg - box ) of human sry gene

    二、研究報告1 、採用pcr技術，以特異擴增人sry基因hmg - box保守區的一對特異引物擴增了虎紋蛙sox基因，優化了擴增條件。
  6. 2. using a pair of degenerate primers based on the conserved region, hmg - box, of human sry gene, eight different fragments were amplified from both female and male rana rugulosa wiegmann then cloned by using pmd18 - t vector and sequenced

    2 、參照人sox基因設計了一對兼并引物，擴增了虎紋蛙的sox基因，並對擴增產物進行了克隆和測序。
  7. The conversed 120 bp gene region contains an intragenic control box related to the gene tanscription

    雙維管束亞屬植物長度在658刁28hp ，白皮松則為49952hp 。
  8. Biological rule of inserts and rh box needs farther research. our research showed that gene sequences of the oriental were different from that of caucasian. designing primers according to rh dna sequence derived from caucasian could not discover the influence factors of rh d gene expression and inheritance characteristics

    筆者認為，東方人種有著不同於高加索人的rh血型基因u ，文獻公布的rhdna序列來源於高加索人種，據其設計引物進行的研究，不能完全揭示中國人d基因表達的影響因素及遺傳學特徵。
  9. It is suggested that 538bp sequence of ast gene 5 " end had been cloned after the 138bp fragment was linked up with the 706bp fragment. the analysis of 538bp sequence with the software of promoter prediction indicated that there maybe exist four transcriptional initiator sites, one caat - box and two gc - boxes

    將該片段與706bp的片段對接后，表明克隆到了ast基因的上游啟動子的538bp序列，通過promoterpredict軟體進行啟動子的分析，顯示該序列存在可能的四個轉錄起始位點，一個caat框和兩個gc框。
  10. The predicated amino acid sequences contain two conserved functional domains : a dna - binding domain ( hmg - box ) and a transactivation domain. the conserved motif of group b homology lies immediate adjacent to c - proximal region of the hmg - box. similar structure and identity of sox2 gene among mammals, birds, amphibians and reptiles suggest that sox2 gene have evolutionary conserved roles

    進一步分析表明，已巴灘2編碼的238個氨基酸多膚鏈含有兩個保守的功能區域:位於n端的hmg盒區（ 1一78aa ）和位於c端的轉錄激活區（ 131一236aa ） ，以及一個保守的特徵性b亞族同源區域（ 79一90aa ）與hmg盒區的c端相連。
  11. ( 2 ) deletions of four different lengths were conducted using pcr amplification with the information of sequence of pdf 1. 2 gene promoter. these mutated promoters were fused to the gus reporter gene and introduced into tobacco plants. the results of gus activity driven by these different constructs showed that the promoter sequence between positions - 300 and - 243 ( containing a gcc box and a g box - like sequence ) was an essential ja - responsive element region to activate the expression of gus reporter gene, and the - 300 bp position was defined as the boundary of the minimal functional promoter in response to ja signaling

    （ 2 ）對該啟動子的5 』端進行不同長度的缺失突變，突變的啟動子與gus構建的融合基因在煙草中受meja誘導的瞬時表達結果表明，該啟動子中- 300 - 243bp區域（有一個gccbox和一個gbox - likesequence ）是其應答meja處理所必須的區域，並將- 300bp作為該啟動子應答ja信號的最小區域的邊界位置。
  12. Escherichia coli promoter, which could initiate transcription of a gene, was mainly consisted of two conserved sequences, - 10 box and - 35 box, and spacer between them, whose length is changeable

    大腸桿菌啟動子能起始基因的轉錄，它主要由兩段比較保守的序列片斷- 10框、 - 35框和它們之間一段長度可變的堿基序列組成。
  13. Part two : studies ; l. the sox gene of dinodon refozonatum was amplified by using a pair of primers which can amplify the conservative motif ( hmg - box ) of human sry gene. the amplification band was observed in both male and female dinodon refozonatum, whose length was consistent with that of human sry gene, which about 220bp. the result of sscp analysis showed that there were many differences in the sox gene sequence between dinodon refozonatum and human, and there was a few differences between male and female dinodon refozonatum. 2. using a pair of degenerate primers based on the conservative region, hmg - box, of human sry gene, six different fragments were amplified from either female or male dinodon refozonatum, then cloned by using pmd18 - t vector and sequenced

    結果顯示： （ 1 ）赤鏈蛇基因的擴增片段與人sry基因擴增片斷大小相同，為220bp左右； （ 2 ）雌、雄赤鏈蛇sox基因的擴增片段大小雖然與人的相同，但其單鏈遷移率與人的有較大差異，而且雌雄個體間有明顯差異，預示該基因的dna序列在雌雄個體中可能有差異； 2 、參照人sry基因hmg - box保守區的序列，又設計一對兼并引物，擴增了赤鏈蛇的sox基因，並對擴增產物進行了克隆和測序。
  14. 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。
  15. By sequencing random - selected clones from the library and using bioinformatics, 54 novel expressed sequence tags ( ests ) were obtained, in which there were 14 full - length cdnas, including peroxiredoxin gene, hmg - box gene, ubiquitin gene, signal recognition particle, acetyltransferase gene and lysozyme gene

    有14個克隆包含有完整的開放閱讀框，其中包括抗氧化物酶基因prx 、 dna結合蛋白基因、泛素基因、信號識別蛋白基因、溶菌酶基因和乙酰基轉移酶基因等具有重要生物學功能的基因。
  16. In transgenic tobacco plants, the transient - expression assay of the chimeric gene ( 4 x gcc - 35s min : : gus ) demonstrated that the 4 x gcc - 35smin promoter could respond to meja treatment and the gcc box is an important element in response to ja signaling. moreover, this experiment results would be meaningful to improve the crops characterization of resistance against various environment stresses or to study the regulation of gene expression in transgenic plants

    （ 3 ）以反向的4xgcc重復序列（ placzi 4xgcc （ 》作為placzi4xgcc的突變體， 6半乳糖苦酶活性分析的結果表明，與野生型的相比，突變的gcc元件不能與jerfi 2 3 4相互作用， p半乳糖苦酶實驗不能呈現出藍色反應；證明gccbox與jerf 2 3 4是特異性結合。
  17. 2. an anther specific chimaeric male sterile gene expression box with a enhanced promoter ( ta29 ) driving coda gene was constructed and the expression box was inserted into binary vector p3301 that contains a l - phosphinothricin ( ppt ) - resistant selective marker gene and - glucuronidase ( gus ) reporter gene in t - dna region

    以增強的ta29啟動子驅動克隆的coda基因，構建成花藥特異性嵌合基因表達盒；將此表達盒插入雙元載體p3301 ，構建成以ppt抗性基因為選擇標記，以gus為報告基因的植物表達載體。
  18. Cloning and expression of a mads box gene from bitter melon momordica charantia l

    同源基因的克隆與序列分析
  19. On the basis of analyzing relative conservative series of promoters in eukaryote ' s gene, the conservative property of tata box 、 caat box and gc box in the promoters of eukaryote ' s gene and there statistical truth are used in this paper, combined with evolutionary nn to build recognition model of promoter in eukaryote ' s gene, emulate computer program was designed too

    本文在分析了真核生物基因啟動子的相對保守序列的基礎上，利用真核生物基因啟動子的tata盒、 caat盒和gc盒的相對保守性和其統計學事實，結合進化神經網路建立了真核生物基因啟動子的識別模型，並且設計了計算機模擬程序。
  20. Cloning and structural analysis of flower development associated mads - box gene fragment in seedless litchi

    柑桔轉化酶基因家族新成員的克隆和序列分析
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