重陽子 的英文怎麼說

中文拼音 [zhòngyángzi]
重陽子 英文
fatmonk
  • 重 : 重Ⅰ名詞（重量; 分量） weight Ⅱ動詞（重視） lay [place put] stress on; place value upon; attach im...
  • 陽 : Ⅰ名詞1 （太陽; 日光） the sun 2 （山的南面; 水的北面） south of a hill or north of a river 3 （中...
  • 子 : 子Ⅰ名詞1 （兒子） son 2 （人的通稱） person 3 （古代特指有學問的男人） ancient title of respect f...
  • 陽子 : honna yoko
  1. Space environment threaten orbited spacecraft " s safe functioning and astronaut " s health, influence greatly communication depended on based - space way, airmanship orientation, military detection, aim identification, weather observation and source exploration and so on by all sorts of function ( magnetic storm, solar proton event and so on )

    空間環境通過各種效應（如磁暴、太陽質子事件等）對在軌航天器的安全運行及航天員的健康構成了嚴重的威脅，對依賴于天基手段的通信、導航定位、軍事偵察、目標識別、氣象觀測、資源勘探等等均有重要影響。
  2. Remarks : the weekly cleaning operations scheduled on chung yeung festival october 19 will be re - scheduled on the other day in the week

    *備注原定或重陽節（ 10月19日）進行的泳池大清潔將另行安排在同周的其他日子進行。
  3. Which is a homonym of the word for " top "

    重陽節秋高氣爽，亦是登高遠足的好日子。
  4. After the protein was electrophoresised and purified, the protein activity was detected by elisa, the protein activity of vp1 is higher than vp0 vp3. at last, the activity of vp1 made in our lab was detected with the agentia made in our lab

    將陽性重組子轉化到大腸桿菌er2566細菌內，用ipig進行誘導表達蛋白，蛋白經電泳、純化，然後用elisa方法檢測蛋白活性， vp1蛋白活性相對高於vp0 、 vp3 。
  5. The positive colonies that grew on the ampicillin ( amp ) plate ( lb agar medium contaning 100 g / ml amp ) were screened and identified. sds - page and western blot analysis were performed to study the expression profiles of target gene cein in e. coli

    從轉化的平板中篩選出陽性重組子，進行不同iptg濃度和不同誘導時間的表達研究，並利用sds - page電泳和westernblotting蛋白質印跡技術對外源基因cei _ （ 12 ）在大腸桿菌e
  6. The ching ming festival in spring and chung yeung festival on the ninth day of the ninth moon are occasions for visiting ancestral graves

    暮春的清明節和農歷九月初九的重陽節是往掃墓拜祭先人的日子。
  7. Chung yeung is on the ninth day of the ninth lunar month, when many visit their ancestors graves or hike up mountains in remembrance of an ancient chinese family s escape from plague and death by fleeing to a mountain top

    中秋節當晚，男女老幼到公園和郊外燃點彩燈賞月，盡慶而返。暮春的清明節和農歷九月初九的重陽節是掃墓祭祖的日子。不少市民在重陽登山，紀念登高避難的古人。
  8. Chung yeung is on the ninth day of the ninth lunar month, when many visit their ancestors graves or hike up mountains in remembrance of an ancient chinese familys escape from plague and death by fleeing to a mountain top

    冰輪高揭，家家踏月，男女老幼到公園和郊外燃點彩燈，盡慶而返。暮春的清明節和農歷九月初九的重陽節是掃墓祭祖的日子。不少市民在重陽登山，紀念登高避災的古人。
  9. The rate of single event upset ( seu ) for space - based missions has been predicted by means of ground - based particle accelerator test and simulation calculation based on models of space radiation environment and the interaction of ions with the microelectronic device

    我們採用的方法是用地面重離子加速器模擬實驗和計算機模擬空間輻射環境進行單粒子翻轉率預估計算。引發單粒子翻轉的空間高能帶電粒子環境包括銀河宇宙線，太陽宇宙線和地球輻射帶中的高能質子及重離子。
  10. The top plot depicts the low - energy plasma of solar wind origin, and the bottom plot shows heavy ion intensities associated with the planet

    頂部情節描寫低能離子的太陽風的原產地，以及底部圖謀表明重離子強度與星球。
  11. Zhejiang : buttered pancake, double ninth chestnut cake, zhongzi stuffed with fresh meat, noodles with shrimp and eel, ninbo glutinous rice dumpling, eight treasures in black rice

    浙江的酥油餅重陽栗糕鮮肉棕子蝦爆鱔面紫米八寶飯。
  12. In this paper, we constructed the genomic dna library of nephila clavipes with the vector supercos 1 cosmid

    以dig - oligo2為探針，菌落原位雜交篩選cosmid文庫，得到56個陽性重組子。
  13. The library was rescued with phage m13k07 in order to display scfv on the surface of the phage and to form the recombinant phage antibody library. one of positive scfv clones, named pcsal, was selected with phage - elisa after panning and screening by bull sperm three times. scfv fragment, amplified from pcsa1, was ligated to pmd18 - t vector for sequencing analysis

    取陽性重組噬菌體抗體克隆株pcsa1 ， pcr擴增其scfv基因，篩選重組子進行序列測定，發現其序列符合小鼠抗體基因的一般特徵，並且與幾株抗磷酸膽堿的抗體重鏈和輕鏈可變區序列的同源性達80以上；推測pcsa1scfv針對的抗原是磷酸膽堿類物質。
  14. Recovered the agarose and identified by agarose gelelectrophoresis. the producys of pcr fragments and pcambial303 plasmid ligation were transformed into e. coli ( dh5a ). the result of pcrof positive recombinant and restriction analysis demonstrated that the plant expressing vector of tps is attained

    Pcr產物經回收后，經瓊脂糖凝膠電泳鑒定后，與pcambia1303連接並轉化大腸桿菌dh5a ，陽性重組子經pcr和限制性內切酶酶切圖譜分析，表明已獲得海藻糖- 6 -磷酸合成酶基因的植物表達載體。
  15. The pcr products were purified and linked with pmd 18 - t vector respectively. the positive recombinants were selected and digested with double restriction enzymes respectively. goat fsh - a and p subunit genes which had sticky ends were purified and linked respectively with pf which also had the corresbonding sticky ends and were purified

    將所得的山羊fsh - 、亞基基因分別用加相應限制性內切酶酶切位點的引物大量擴增，回收后與pmd18 - t連接，篩選出陽性重組子，大量雙酶切回收獲得帶粘性末端的山羊fsh - 、亞基基因，將它們分別與同兩個酶大量雙酶切回收獲得的帶粘性末端的pf質粒進行連接，篩選陽性重組子。
  16. Fasl - ecd coding sequence is subcloned into pet - lla expressing vector, recombinant expression vector are named as pet - fasl - ecd. this plasmid is introduced into e. coli bl21. after induction with 1mmol / l iptg, the protein expression is analyzed and confirmed by coomassie - stained sds - page

    用pcr和酶切鑒定的方法篩選出陽性重組子，將陽性重組子以ilnlnol幾iptg進行誘導表達，以sds一page分析fasl胞外區的表達。
  17. Ii ) two fragments ( about 240bp and 130bp ) were amplified from human keratinocytes total rna by rt - pcr. the recombinant pm - hpabl and pm - hpabs plasmids were constructed by inserting 240bp and 130bp pcr products into pmd 18 - t vector, respectively. the recombinants were identified by restriction enzyme analysis and dna sequencing, iii ) two orfs ( > 100bp ) were found in the insert sequence of pm - hpabl

    應用smartpcr試劑盒和簡並引物從人皮膚角質形成細胞cdna中擴增到長分別為24obp和13obp左右的2種片段，將它們插入pmd18一t載體，用酶切法初步篩選陽性重組子pm . hrabl和pm一hrabs ，對陽性重組子進一步作測序鑒定。
  18. Sequence analysis shows that they share 98. 75 % similarity at the dna, and 98. 67 % at the protein level. ns2 gene was cloned into the multiple cloning sites of prokaryotic expression vector pgex - 6p - l. the recombinant plasmid pgex - 6p - ns2 was constructed and transformed to the competent cell bl21 ( de3 ) plyss, positive bacterium strain was induced by iptg

    將ns2基因插入到原核表達性質粒pgex - 6p - 1的ecor 、 bamh多克隆位點之間，將重組原核表達質粒pgex - 6p - ns2轉化到bl21 （ de3 ） plyss感受態細胞中，獲得了表達ns2基因的陽性亞克隆重組子，在含amp的lb液體培養基中培養，經iptg誘導表達，用sds - page分析表達產物。
  19. Therefore, a - amylase has been used widely in many industrial fields, such as glucose production, beer brewing, fermentation trade, textile industry, and so on. the study on a - amylase is one of the most active fields in enzyme industrial fields. with the development of biotechnology, more and more scientists and researchers attempt to use dna shuffling technology to breed, screen and even " create " new a - amylase genes with higher activity and other new characters

    設計引物時，上下游引物5 』端分別添加了kpn和bamh酶切位點，克隆得到的基因片段和質粒載體都用kpn和bamh進行雙酶切后，進行酶連、轉化、篩選得到陽性重組子，經過藍白斑驗證、單酶切驗證、雙酶切驗證、 pcr驗證等一系列的驗證后進行測序。
  20. 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

    經瓊脂糖電泳檢測，將大小與預計分子量一致的片段純化后連接到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。
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