核甘酸 的英文怎麼說

中文拼音 [hégānsuān]
核甘酸 英文
nucleic acid; nucleotide
  • 核 : 核構詞成分。
  • 甘 : Ⅰ形容詞（使人滿意的; 甜） pleasant; sweet Ⅱ動詞（自願; 樂意） be willing to; be contented or sati...
  • 酸 : 酸構詞成分。
  1. In these chloroplasts carbon dioxide combines with phosphoenolpyruvate to form oxaloacetic acid, which is transported to the bundle sheath cells, where the carbon dioxide is released, then fixed by the enzyme ribulose bisphosphate carboxylase to form glycerate 3 - phosphate, the first step in the calvin cycle

    在葉肉細胞的葉綠體中二氧化碳與磷酸烯醇丙酮酸結合形成草酰乙酸，后被運到鄰近的維管束鞘細胞，在那裡二氧化碳被釋放，后被核酮糖二磷酸羧化酶固定形成3磷酸甘油酸，這是卡爾文的循環第一步。
  2. Among the genes, there were genes directly related to liver regeneration : fetuin, cathepsin ; close related to liver function : cytoplamic aspartate aminotranferase, gutathion sulfur transferase ; related to substance and energy metabolism : atp synthetase, ribosomal protein, and related to stress response : haptoglobin, transferrin

    這些基因中有和肝再生有直接關系的如：胎球蛋白、組織蛋白酶；和肝臟功能密切相關的如：胞質天冬氨酸轉氨酶、谷胱甘肽硫轉移酶；與物質能量代謝有關的如： atp合成酶、核糖體蛋白；以及與急相反應有關的如：觸珠蛋白、轉鐵蛋白。
  3. Glycerate 3 - phosphate is the first product of the dark reactions of photosynthesis, formed by the carboxylation and cleavage of ribulose bisphosphate

    甘油3 ?磷酸是光合作用暗反應的一種產物，在二磷酸核酮糖的羧化分解后形成。
  4. Nucleoside and nucleotide analogues are usually long - term therapy, potentially life - long, for people with chronic hepatitis b

    核甘類似物和核甘酸類似物用作治療慢性乙型肝炎，病人一般需要長期甚至終生接受治療。
  5. Clinical observation on pituitrin combinded with nitroglycerin treating hemoptysis caused by pulmonary tuberculosis

    腦垂體后葉素聯合硝酸甘油治療肺結核咯血臨床觀察
  6. Snps : single nucleotide polymorphisms. ( image courtesy of the u. s. department of energy human genome program

    單核甘酸變異。 （影像提供：美國能源部人類基因組計畫。
  7. And the intron had a lot of gt repeated sequence. the dna and protein sequence of this gene was analyzed using the bioinformatics tools. two functional domains were found in the protein

    運用生物信息學手段對3一磷酸甘油脫氫酶基因核酸以及蛋白質序列做出了分析，發現這個基因編碼兩種功能的結構域，磷酸化酶結構域和3一磷酸甘油脫氫酶結構域。
  8. At 250 ? c, the half - life of nucleotides measure in seconds

    在250 ? c ，核甘酸的半生命期僅幾秒鐘。
  9. Snp single nucleotide polymorphism

    單核甘酸多形態現象
  10. Software solution that provides a visual interface to nucleotide mutations

    為核甘酸突變提供視覺介面的軟體解決方案。
  11. Overall, the study participants had an average telomere loss of 21 nucleotides ( structural units ) per year

    總的來說，該項研究的參與者每年平均損失21個核甘酸（結構單位） 。
  12. System - the latest revolution in rapid clinical and non - clinical diagnosis and novel genetic markers to the provision of new veterinary and clinical diagnostic methods for infectious diseases and dna testing services, such as : parentage, pre - natal screening, dna fingerprinting and genetically modified food testing

    基因晶片的研究與開發，帶給快速臨床及非臨床診斷的最新革命新基因標記研究，尤其是單核甘酸多態標記，皆為科學界最前沿的醫學工具。
  13. The effects of glp - 1 ( 7 - 36 ) nh2 on insulin secretion glp - 1 ( 7 - 36 ) nh2 with the concentration of 2. 5nmol / l, 5. 0nmol / l, l0. 0nmol / l, 20. 0nmol / l, 40. 0nmol / l respectively were added to the medium as different experimental groups, 24 hours later, insulin amount are 68. 76 ? 1. 71 72. 30 ? 3. 13 104. 16 ? 5. 57 110. 98 ?. 29 111. 58 ? 0. 65miu / l respectively, and the insulin account is 55. 53 ?. 63miu / lin the control group. there was no significant difference between the groups with 2. 5nmol / land 5. 0nmol / l glp - 1 ( 7 - 36 ) nh2 respectively ; and there was not significant difference among the groups with lo. onmol / l, 20. 0nmol / l and 40. 0nmol / l glp - 1 ( 7 - 36 ) nh2 respectively. but the difference is significant between experimental groups and control group ( p < 0. 05 ). the data show that with the rising concentration of glp - 1 ( 7 - 36 ) nh2, there is an increasing amount of insulin

    對照組培養液中不含g廿一1 （ 7一36 ） nhz ，實驗組培養液中含有20nmol / lglp一1 （ 7一36 ） nhz ，培養24h后，用0 . 25 %胰蛋白酶消化胰島分散細胞，塗片后利用針對胰島素mrna的寡核甘酸探針進行細胞原位雜交， dab顯色，高清晰度病理圖文分析系統（ highpathologiealimageanalysissystem ， hp認s ）對細胞著色的平均光密度（ mean即tiealdensity ， mod ）量化分析，觀察實驗組和對照組胰島素mrna的表達情況。
  14. The full length cdnas of 17 - hsd1 and 17 - hsd3, 17 - hsd8 were obtained by library screening and race, respectively. expression patterns ( tissue distribution ) of three types 17 - hsds were checked by rt - pcr and northern blot. the recombinant constructs of 17 - hsdl / pet blue2 and 17 - hsd8 / pcdna 3. 1 were made and subsequently transformed into the corresponding host expression cell of ( de3 ) placi and mammalian hek 293 cell

    首先從genebank下載在其他脊椎動物中已被克隆17 - hsd1 ， 17 - hsd3的氨基酸和核甘酸序列，並在序列保守區域設計簡並引物，然後分別以羅非魚卵巢和精巢cdna為模板進行rt - pcr擴增得到17 - hsd1 ， 17 - hsd3的中間片段。
  15. The genetic diversity of p. sibirica, which is represented by 98 individuals collected from all 5 subpopulations, investigated with rapd markers. 77 loci were selected by fourteen 10 - mer primers, of which 76 were polymorphic. the percentage of polymorphic loci ( ppb ) of five subpopulations was 70. 13 %, 77. 99 %, 62. 34 %, 67. 53 %, and 61. 04 % respectively

    用rapd分子標記對叉毛蓬5個亞居群共98個個體進行了遺傳多樣性檢測， 14個10堿基寡聚核甘酸引物共檢測到77個位點，其中多態位點76個，多態位點比率為98 . 7 。
  16. Clinical value of lam - igg indiagnosing pulmonary tuberculosis

    阿拉伯酸甘露聚糖檢測對肺結核的診斷價值
  17. Then, a piece of degenerate primer was designed according to the conserved amino acids of glycine betaine abc transporter system glycine betaine - binding protein as a reversed primer. combined with the opuaa - up, a 2. 3 kb fragment was obtained through pcr. blast result showed a fragment which contained the partial opuaa, the whole opuab and partial opuac sequences were obtained

    再次，根據甘氨酸甜菜堿atp轉運系統底物結合蛋白的氨基酸保守序列設計下游簡並引物，與atp結合蛋白的上游簡並引物組合，經pcr擴增獲得2 . 1kb的條帶，測序后通過blast比較，結果顯示獲得atp結合蛋白基因的部分序列、通透酶的全部編碼序列和部分甘氨酸甜菜堿結合蛋白基因的核苷酸序列。
  18. Beth showed 56 % identity to the opud of bacillus subtilis and belonged to bcct family. its putative promoter region was highly homologous to b - dependent promoter of b. subtilis. a 2. 6 kb fragment including the beth gene was subcloned into puc18 and transformed into the e. coli mkh13, colonies appeared on the plate of the selective m9 medium

    將包括整個beth基因orf框及可能的啟動子核苷酸序列在內的2 . 6kb的片段克隆到puc18載體上，轉入到大腸桿菌甘氨酸甜菜堿缺失株mkh13中，使該菌株能夠在含甘氨酸甜菜堿的高鹽m9培養基上生長，而對照實驗不能生長。
  19. The insert dna fragments are 7kb and llkb, respectively. two subclones that were designated pgr3h1 and pgr7h1 and can increase glyphosate resistance of e. coli jm109 up to 150mm glyphosate were constructed by subcloning the 2. 4kb and 3. 2 kb hind ? / psti fragments of pgr3 and pgr7 into the corresponding sites of pgem - 3zf and pbluescript. sequence analysis of these two subclones revealed a completely identical 1323bp open reading frame that encodes an epsp synthase

    以pgem - 3zf和pbluescript為載體，利用限制性內切酶hind和pst構建這兩個克隆的亞克隆，從中分別得到兩個草甘膦耐受亞克隆pgr3h1和pgr7h1 ，插入片段各為2 . 4kb和3 . 2kb ，對這兩個亞克隆進行序列分析，發現二者均含有一個核苷酸序列完全相同的完整的epsp合成酶基因? ? aroa ，其核苷酸序列長為1323bp ，推導的epsp合成酶由441個氨基酸組成，兩個亞克隆的草甘膦耐受濃度最大可達150mm 。
  20. We confirmed one single nucleotide polymorphism ( snp ) site in the exon 7 of cd226 gene with agt - ggt polymorphism of 307 codon. among ten volunteers, 4 cases are serine and 6 cases are glycine at this codon

    在編碼cd226胞漿區第307位氨基酸的密碼子上存在agt ? ggt單核昔酸多態性（ singlenucleotidepolymorphism ， snp ） ；分別編碼絲氨酸和甘氨酸。
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