genomic 中文意思是什麼

genomic 解釋
基因組的
  1. The results showed as follows : ( 1 ) 6 traits are correlative with genomic factors according to analysis of population genetics and comparison of the coherence of twins. ( 2 ) the hereditary mode of rolling tongue or pointed tongue was the dominant heredity of single gene of autosome, and the can - rolling type or can - pointed type was the dominant character

    本文首次從群體遺傳學、家系分析、典型系譜分析及雙生子分析多個角度並結合多種相關數理統計方法，對6項人類學特徵的遺傳方式進行了探討，初步確定了各項特徵的遺傳方式，評價了各特徵的遺傳與環境的相對重要性。
  2. Degenerate oligonucleotides to highly conserved regions of cucumis melo 1 - aminocyclopropane - 1 - carboxylic acid ( acc ) oxidase gene were used to prime the amplification of fragment of 128bp by ploymerase chain reaction ( pcr ) in samples of genomic dna from fruit of cucumis melo l. cv hetao flesh, which was cloned into plasmid vector pmd - 18 - t. the clon of antisense orientation were selected, and it was inserted downstream of camv35s promoter and enhancer " " of tmv into the plant expression vector pbinyxw, antisence expression vector pbinya was constructed. at the base that pollination and fertilization of cucumis melo l. cv hetao was studied, using pollen tube pathway transformate cucumis melo l. cv hetao, 76 fruit had been obtained, moreover, hardness and content of sugar were analysed

    本實驗以河套蜜瓜果肉基因組dna為模板，用甜瓜acc氧化酶基因特異寡核苷酸鏈為引物進行pcr擴增，得到128bp的擴增產物。將得到的擴增產物克隆到質粒載體pmd - 18 - t上，篩選反向克隆，然後將其反向構建到植物表達載體pbinyxw的camv35s啟動子和tmv增強子「 」的下游，構建成反義表達載體pbinya 。並在對河套蜜瓜授粉受精生物學研究的基礎上，通過花粉管通道法轉化河套蜜瓜，共獲76顆瓜，並進行了硬度和含糖量的分析。
  3. Two primers, designed according to the conserved regions of ban gene in arabidopsis thaliana, were used to amplify the ban homologous fragments from the genomic dna of brassica napus, b. chinensisl, b. juncea, a. thaliana and other cultural plants of cruciferae. the very similar pcr fragments were obtained from all the amplifications, which implicated that ban may be a conserved gene existing widely in the genomes of cruciferae. pcr fragments were cloned and confirmed by restriction enzyme digestion

    參照擬南芥（ arabidopsisthaliana ） ban基因與cdna設計引物，對甘藍型、白菜型、芥菜型油菜，擬南芥及其它十字花科栽培品種的基因組dna進行pcr擴增，均擴增出與擬南芥ban基因擴增片段大小極其相似的dna片段，提示ban可能廣泛存在於十字花科植物中。
  4. Some tendency of tn5gusa5 transposition were found that all preferred sites of tn5gusa5 in xcc 8004 genomic dna are in at - rich regions ; target sequences of tn5gusa5 have some features that the probabilities of guanine and cytosine are high respectively at the head and tail base of target sequence ; the level of gene transcription does not influence insertion density of tn5gusa5 significantly

    結果表明， tn5gusa5插入位點有一定的規律性： tn5gusa5在xcc8004基因組上傾向于插入低gc含量（ 50左右的區域插入密度最高）區段；插入位點的靶序列有一定的特異性，在靶序列的首位鳥嘌呤出現的幾率高，而在靶序列的末位胞嘧啶出現幾率高； tn5gusa5的插入密度與該區段基因的轉錄水平無明顯關系。
  5. The genomic dna are extracted from alcohol steep sample of tachinidae ( diptera ), by the analysis of experimental results, show that the method is feasible

    目的提出了一種有效的酒精浸泡的雙翅目寄蠅科昆蟲基因組dna的提取方法，通過對實驗結果的分析，表明該方法可行。
  6. Double cross - over strains aved24 and avec9 were obtained after growth of several generations on mym plate with or without antibiotics selection. genomic dna of double cross - over strains aved24 and avec9 were extracted and southern hybridization were performed

    分別提取同源雙交換茵株aved24和avec9基因組dna ，通過薩瑟恩（ southern ） dna印跡雜交，結果證明l
  7. With the improved method of ctab, the genomic dna extracted form plum and other species close to p. mume in genetic relationship could be directly used in pcr amplification, with good results obtained

    選用改良ctab法提取的梅及其近緣種的基因組dna可直接用於pcr擴增分析，且效果良好。
  8. The characteristics of tm - 22 expression presented in transgenic tobacco : 1 ). virus specificity in either homozygote or heterozygote ; 2 ) tm - 22 gene integrated in tobacco genomic dna with single copy and in inheritance and segregation to progenies on the mendel role ; 3 ). transgenic line with tm - 22 promoter ( ptm47 ) showed infected symptoms with cell death distinguished to one with 35s promoter ( ptm49 ) after inoculation with tomv - 2a

    其次，通過氨基酸序列和結構的比較，確定tm - 2 ~ 2基因的編碼蛋白與tomv病毒在抗病反應中相互識別的特異氨基酸及其功能；然後，應用重組dna技術，互換tm - 2 ~ 2基因和tm - 2基因的對應結構域，構建嵌合基因，獲得嵌合蛋白表達的轉化體，驗證tm - 2 ~ 2編碼蛋白中變異氨基酸的作用。
  9. We generated a recombinant eukaryotic gene expressing vector harboring a full - length hgh gene, 2. 4 kb genomic dna with four introns and the signal peptide sequence cloned to the eukaryotic gene expressing vector pcdna3. 0

    我們直接將含有4個內含子和自身信號肽的2 . 4kb全長人生長激素基因直接克隆至真核表達載體pcdna3 . 0 ，然後利用脂質體轉染家蠶bmn細胞，瞬時表達hgh 。
  10. Cloning of ctsox2 gene shows the validation of rpgw - pcr used for isolating genes from the digested genomic dna

    C心以2基因的hmg盒區外的序列信息可以進一步研究它的功育旨。
  11. There exist successive deletions in the sequence of the genomic dna of kale and kohlrabi, compared with that of brussel sprouts

    相對抱子甘藍基因組dna而言，羽衣甘藍和球莖甘藍在序列中發生了多處大量堿基的缺失。
  12. Primers were designed according to the sequences of atcal, bocal, bobcal and boical gene, and pcr amplifications were performed with the genomic dna of brussel sprouts, kale and kohlrabi respectively, pcr fragments of about 1. 6kb were obtained and designated correspondingly as bogcal5 ", boacal5 " and boccal5 "

    根據擬南芥atcal 、結球甘藍bocal 、花椰菜bobcal和青花菜boical基因設計引物，對蕓薹屬植物抱子甘藍、羽衣甘藍和球莖甘藍的基因組dna進行pcr擴增，均得到一段約1 . 6kb大小的pcr產物，分別命名為bogcal5 』 、 boacal5 』和boccal5 』 。
  13. At first. then eight a - amylase gene fragments were cloned with the genomic dnas as templates by routine pcr. following that, these gene fragments and plasmid vectors, pbluescript ii ks + and puc18, were cut by bamh i and kpn i. the prepared insert dna and vector dna were linked by t4 dna ligase

    利用vectornti6 . 0軟體，對所克隆的序列用相鄰接點法（ neighborjoining州j ） method ）進行多序列比對，分析其同源性，並構建基因進化樹。
  14. At the same time, using the genomic dna of blast sensitive cultivar c039 as a template, two fragments were obtained that were the same large dna sequence as resistance cultivar c101a51. one sequence has conserved motifs of nbs - lrr type resistance genes, the other sequence can " t read through

    同時本研究還以感病品種c039的基因組為模板，也擴增得到與c101a51抗病品種中抗病基因同源序列同樣大小的dna片段，但一個有抗病基因的保守結構，另一個片段不能通讀。
  15. All kind of oligonucleotides ( 16 sense primers, 8 antisenset primers, 128 different primer combinations in all ) were designed from the conserved motifs glpl and cfly ( distance between them is approximately 210bp ) which existed only in the type of nbs - lrr resistance gene and used as primers for scanning the genomic dna. no specific products ( which is approximately 210bp in length and obtained from genomic dna containing ht gene ) was obtained though amplified products of approximately 500 - looobp appeared in six different primer combinations

    依據nbs - lrr類r基因特有的兩個保守序列glpl和cfly （兩者相距約70個氨基酸）合成所有可能的簡並寡核苷酸引物（左引物16個，右引物8個，共組成128個引物組合）對玉米基因組dna進行擴增的結果表明：在6個引物組合中得到了擴增產物，產物長度在500 1000bp之間；沒有獲得特異性擴增產物（指僅從含ht基因材料中得到，長度約210bp的dna片斷） 。
  16. The chilopoda and diplopoda are monophyletic group respectively. although there are some limitations, the mitochondrial dna as a model system is being used as a powerful tool in phylogeny analysis. it is the only molecular marker that can be used in the phylogenetic studies at genomic level

    線粒體dna基因組全序列作為研究動物系統發生的模式系統，雖然有一定的缺陷，但仍是生物學家研究系統進化最有力的工具，它是目前唯一可以提供基因組水平上進行系統發生研究的分子標記。
  17. Tsarg2 with 1 233 bp length was composed of 6 exons and spaned about 115 kb of genomic dna, the putative protein encoded by this gene was 305 amino acid with a theoretical mass of 34 751 and with no significant homology with any known protein in databases. a kind of nucleoprotein was the most impossible

    Tsarg2基因的cdna全長為1233bp ，包含6個外顯子，基因組跨越115kb ，編碼由305個氨基酸組成的、分子量為34751的蛋白質，與已知蛋白質無明顯同源性，其最大可能是一種核蛋白。
  18. Used the genomic dna extracted by low melting - point agarose embedding method as pcr template, the full length of structural genes of bacillus subtilis bio operon were gained by long pcr method

    將該方法提取的基因組dna稀釋100倍作為模板，採用長距離pcr方法，獲得了枯草桿菌生物素操縱子基因全長。
  19. Genomic analysis of parasitic human pathogens, particularly plasmodium falciparum, and leishmania major

    人類寄生性病原體的基因體分析，特別是瘧原蟲與利什曼原蟲。
  20. Among the three methods used in the experiment of dna extraction, only ctab, adding pvp in the dna isolation step, had effectively reduced the disturbance from fiber or other plastids and extracted suitable genomic dna as template for rapd process. pcr amplifications were performed in a final volume of 25 mm3 containing 0. 5 units taq polymerase, 2

    通過在抽提緩沖液加入2的pvp 、並用異丙醇和乙醇沉澱基因組dna等改良措施， ctab法能避開大量纖維、多糖的影響，有效地從不同屬種的棕櫚科植物的幼嫩葉片中提取並純化了適合rapd的基因組dna 。
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