瓊脂片 的英文怎麼說

中文拼音 [qióngzhīpiān]
瓊脂片 英文
agar block
  • : 名詞1. [書面語] (美玉) fine jade 2. (姓氏) a surname
  • : 名詞1. (動植物所含的油質) fat; grease; tallow 2. (胭脂) rouge 3. (姓氏) a surname
  • : 片構詞成分。
  1. The value of diploid peak before gi was larger in the higher concentration and longer time of arsenic trioxide on floe cytometry

    從凋亡細胞中提取dna段在2糖電泳,顯現典型凋亡dna段142bp 、 174bp梯形帶。
  2. Cut agar agar into small pieces, soak in the other half of water. boil with medium heat, stir constantly. remove from heat when agar agar is totally dissolved

    剪成碎,泡入到餘下的冷水中,用中火煮沸,多多攪拌,到完全融解后熄火。
  3. The 2nd pair of primers was designed according to the sequence of strain th - 98 collected in genbank. concentration of tp was analyzed after amplification invitro by rt - pcr, purified by low melt agarose and labeled by digoxigenin

    根據genbankth - 98株序列設計第2對引物,應用rt - pcr方法體外擴增該段(命名為tp ) ,糖凝膠純化后測定其濃度和純度,進行非放射性地高辛標記。
  4. Extensive mitochondrial dna polymorphisms were found among lagurus lagurus, mus musculu , rattus norvegicus and mice. the findings will help us to understand the dispersion and evolution of these animals

    通過糖凝膠電泳對這些段進行測定,同時估算出草原兔尾鼠線粒體dna的長度約為16 . 6kb 。
  5. The results also explained that it was feasible that the genomic dna of bacillus subtilis were extracted and gained large dna fragments by low melting - point agarose embedding method

    說明以低熔點糖包埋法提取枯草桿菌基因組dna ,並獲得較大的dna段,是完全可行的。
  6. 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

    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:低熔點糖包埋法提取的基因組dna段明顯大於后兩種方法,採用0 . 5糖凝膠電泳3h ,仍然跑不出加樣孔。
  7. Cells were then harvested by centrifugation and the pellet was resuspended in phosphate - buffered saline ( pbs ) containing 5 mm edta. after sonication, debris was removed by centrifugation at 10000 x g for 15 min at 4

    挑取轉化后的大腸桿菌提取質粒, ecori和hindln酶切質粒進行鑒定,搪電泳顯示含有大約800kb的目的段。
  8. I and hindlll respectively. after the digested products were run via agarose gel electrophoresis and transferred into nylon membrane, the southern blot was carried out using the cdna of rubber tree etrl as probe. the result of the southern blot showed that a hybridization band ( - 3. 0kb ) turned up from the ecor i digested product and another band ( - 4. 8kb ) turned up from the hindi ]

    從橡膠樹pr107品系的嫩葉提取基因組dna ,用限制性內切酶ecor 、 hinofll分別酶切,糖凝膠電泳分離並轉膜后,用克隆的橡膠樹etri基因的cdna段作探針進行southern雜交分析,結果表明, ecor酶切在約3 okb處有一條雜交帶出現, hi 。
  9. A 1. 7kb fragment encoding ge of prv fa strain was obtained by pcr from plasmid ppge templated using a pair of the designed primers containing ecori and bamhi ' sites. the ge gene fragment cutted with ecori and bamhi was inserted into the expression plasmid pbv220 including these two endonuclease sites for constructing the recombinant plasmid pbvge. strain dh5a of e. coli contain pbvge was induced at 42 for 4 - 6hr after incubation with vigorous shaking at 30 for 3hr or so

    以質粒ppgedna為模板, pcr擴增出1 . 7kb的ge基因完整段,將擴增產物以ecori和bamhi雙酶切后,插入原核表達載體pbv220的p _ rp _ l啟動子下游的ecori和bamhi位點間,得到重組表達質粒pbvge ,轉化了pbvge的大腸桿菌dh5a經溫敏誘導表達后,用sds - page和western - blot ,以及雙擴散來檢測,結果表明prvfa株ge基因在原核載體上得到高效表達,表達產物約占總蛋白的17 。
  10. Agarose gel electrophoresis video clip wmv format, window media player required

    糖凝膠電泳示範段wmv格式,需用window media player播放
  11. Textile fabrics - determination of antibacterial activity - agar diffusion plate test

    紡織織物.抗菌活性的測定.擴散木試驗
  12. Textile fabrics - determination of antibacterial activity - agar diffusion plate test iso 20645 : 2004 ; german version en iso 20645 : 2004

    紡織織物.抗菌活性的測定.擴散木試驗
  13. The purified products were cloned into pgem - t - easy vector successfully, the cloned plasmids were transformed into e. coli. tgl. the specific recombinant plasmid was identified by molecular weight, pcr and restriction endonuclease analysis. the results indicated that the resultant construct contained the gene of interest hn at right orientation of the insert

    糖電泳檢測,將大小與預計分子量一致的段純化后連接到pgem - t - easy克隆載體中,再轉化大腸桿菌tgi感受態細胞,得到的轉化子經分子量比較、 pcr鑒定和酶切分析篩選陽性克隆。
  14. The purified production was cloned into pmd18 - t vector. the cloned plasmids were transformed into jm109. the specific recombinant plasimid was identified by molecular weight, pcr and restriction endonuclease analysis. the results indicated that the resultant construct contained the gene of ibdv a fragment at right orientation

    糖電泳檢測,將大小與預計分子量一致的段純化后連接到pmd18 - t載體中,再轉化到jm109感受態細胞,得到的轉化子經分子量比較、 pcr鑒定和酶切分析篩選陽性克隆,結果表明,得到的陽性重組子中含有a節段全長基因,插入到載體中的方向正確。
  15. Methods : the qualitative analysis was used by the filter papers, and the quantitative analysis was done by tube method

    方法:採用了濾紙擴散法進行定性試驗,試管二倍稀釋法和平板擴散法進行定量試驗研究。
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