k-dna 中文意思是什麼

k-dna 解釋
acid]動質脫氧核糖核酸
  • k : （pl Ks K s; ks k s ）1 英語字母表第十一字母。2 K字形物體[記號]。3 一個序列中的第十一〈若 J 略去...
  • dna : 1. deoxyribonucleic acid 【生物化學】去[脫]氧核糖核酸。2. deoxypentose-nucleic acid 去[脫]氧戊糖核酸。
  1. An establishment gram institute contains " the k factor " to be able to produce the strong effect immune body, suppression virus activeness, causes viral dna to be unable to duplicate, routs the cause of disease parent substance at one fell swoop, causes the virus to burst the death, never recurs

    安立克kj劑"系列藥物排出的病毒主要聚集在這個部位。安立克所含的「 k因子」能產生強效的抗體，抑制病毒活性，使病毒dna無法復制，一舉擊潰病原母體，使病毒破裂死亡，永不復發！
  2. Composition : 8 essential amino acids, vitamins c, a beta - carotene, b1, b2, b6, b12, e k, niacin, panthothenic acid, folic acid, biotin, choline, inositol, paba, chlorophyll, chlorella growth factor nucleic acids dna rna

    日本食品分析中心在檢驗中證實"紅日牌日本綠藻" ，含有蛋白質葉綠素綠藻精c . g . f多種維他命礦物質以及人體所需的各種氨基酸等，因此，可說是營養最均衡的保健品。
  3. A greedy algorithm for aligning dna sequence. jounal of computational biology, 2000, 7 12, 1 2 : 203 - 214. 9 singh r k, dettloff w d, chi v l et al

    基於這一體系結構特點，本文對megablast程序的流程進行了優化，採用對庫造表的策略，實現了計算和輸出的重疊。
  4. Extraction of large - fragment genomic dna in order to gain dna template of pcr amplification ( long pcr amplification and salvage pcr amplification ) which was high purity and large fragment, three methods were used to extract genomic dna of bacillus subtilis, i. e. low melting - point agarose embedding method, sds - proteinase k - phenol chloroform extraction method and bacterial genomic dna extraction kit method. the genomic dna of bacillus subtilis were gained by these methods, and the operated programs of the methods were improved. the results showed that the genomic dna extracted by low melting - point agarose embedding method were obviously biggest than that of another two methods

    大片段基因組dna的提取為了獲得用於pcr擴增（長距離pcr擴增和分段pcr擴增）的高純度、大片段（至少為pcr產物長度的4倍）的dna模板，應用三種方法：低熔點瓊脂糖包埋法， sds -蛋白酶k -酚氯仿抽提法和細菌基因組dna提取試劑盒法，分別提取獲得了枯草桿菌基因組dna ，並對3種方法的操作程序進行了不同程度的改進，結果表明：低熔點瓊脂糖包埋法提取的基因組dna片段明顯大於后兩種方法，採用0 . 5瓊脂糖凝膠電泳3h ，仍然跑不出加樣孔。
  5. Constructing cdna expressing library of erythrocytic plasmodium falciparum from hainan : the total rna was obtained by using. triplix kit. a modified oligo ( dt ) primer ( cds ffi pcr primer ) was used in the single - stranded ( ss ) dna synthesis reaction. the ss - dna was reversely transcripted from total rna. double - stranded ( ds ) cdna was amplified by long - distance ( ld ) pcrafter the digestion with proteinase k and sfi i, the cdna with no less than 200bp was collected and purified by glass - milk kitthe library was constructed after the ligation of cdna to tiplex2 phage particle packaged with the packaging extract system in vitro. a high titer and high recombinant ratio of cdna library was constructed

    構建惡性瘧原蟲海南株紅內期cdna表達文庫提取紅內期惡性瘧原蟲海南株總rna ，直接以總rna為模板使用cdna文庫構建試劑盒，首先反轉錄合成ss一dna ，再擴增合成ds一dna （ cdna ） ，對擴增產物用蛋白酶k消化及左z丁i酶切，抽提蛋白、去除rna后，用玻璃奶試劑盒純化、回收20obp以上的片斷，經與載體連接再用蛋白包裝物包裝后形成未擴增文庫，最後擴增完成惡性瘧原蟲海南株紅內期cdna表達文庫的構建。
  6. 2 ) the method of proteinase k isolation and the method of ctab isolation had been compared carefully while extracting the genome dna from crickets. the result showed the method of proteinase k isolation of total dna was more suitable for the extraction of total dna from insects of grylloidea

    2 ）在提取蟋蟀總科昆蟲的基因組dna時，比較了ctab法和蛋白酶k法兩種方法，結果顯示蛋白酶法更適用於蟋蟀總科昆蟲的基因組則a的提取。
  7. In this paper, the approach of rapd was used to study 57 species of crickets, which belong to 26 genera, 7 families, in order to discuss their taxonomy status and gentic relationships in molecular level, and enrich the research of molecular systematics in grylloidea. the genome dna of the 57 species were extracted by the method of proteinase k isolation of total dna

    蟋蟀總科的分子系統學的研究也主要集中在個別種種內或種間mtdna多態性方面及個別種同工酶的研究上，而利用rapd技術進行蟋蟀基因組dna多態性方面的研究在國內外更少，國外僅見chu ， j
  8. The orf1 proteins of all four chinese senv isolates had two motifs ( ftl and yxxk ) which were conserved in replication - associated proteins. in all four chinese senv isolates, the putative non - structure orf2 protein had a cav - like region. the putative orf3 protein had a serine - rich tract preceded by a cluster of basic amino acids ( r and k ). database scaning suggested this region had high a percentage of homology with dna topoisomerase i protein of d. melanogaster, and might play an important role in the replication of such single - stranded dna viruses

    所有這四個中國分離株，均保留了o即1中與復制有關的保守序列（ ftl和yxxk ） :在推測是非結構蛋白的orfz中均含有cav樣保守區w 『 x7一h一x3一c一xl一c一xs一h ; orf3蛋白的堿性氨基酸（精氨酸和賴氨酸）簇后緊接著一個富含絲氨酸的區域，與d . molanogaster的dna拓撲異構酶i有一定的同源性，推測在單鏈dna的復制中起作用。
  9. Genome dna of all blood samples were extracted by using erythrocyte lysis solution and pcr buffer / nonionic detergent / proteinase k. a 109bp fragment was amplified from the human genome dna. 2. in 166 han samples, 19 ( 11. 45 % ) heterozygous genotypes of codon 54 mutant allele were found by pcr - sscp

    用紅細胞裂解液和pcr緩沖液非離于去污劑蛋白酶k兩種自配試劑成功地提取了所收標本的人白細胞基因組dna ，並以此為模板成功擴增出預期的109hpmbl目的基因片段。
  10. Method to collect respectively 180 unrelated males " venous blood 500ul, who lived in shanxi province, 120 unrelated mongolians " venous blood 500ul, who lived in the inner mongolia autonomous region, and the blood is anticoagulant with edta, then to extract dna by using the method of phenol - chloroform after ingested by proteinase k at 56 and amplify the dys413 site by using pcr

    方法採集180例山西漢族和120例內蒙古蒙古族男性無關個體靜脈血各500ul ， edta抗凝，用tkml液反復洗滌至無色，加入2蛋白酶k緩沖液180ul ，蛋白酶k （ 20mg ml ） 20ul ，在56消化至液體清亮為止，用酚-氯仿法抽提dna ， pcr擴增dys413位點， 6非變性聚丙烯酰胺凝膠電泳， 1硝酸銀染色分型。
  11. Using pcr technology, a 2. 4kb dna fragment, part of tryptopanase operon, containing a promoter, a regulator gene tnac located downstream of the promoter and a desired tryptopanase gene tnaa which can be expressed by the promoter from e. coli k - 12, was cloned to pmd18 - t vector. the dna sequence is the same as which was published on science

    為了證明質粒上的基因能表達出有活性的色氨酸酶，將這個dna片段克隆到pet28c質粒的bamhi和hind位點上，使該片段受t7rna聚合酶的啟動子控制，然後轉化噬菌體de3的溶源菌bl21 （ de3 ） 。
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