gene product 中文意思是什麼

gene product 解釋
基因產物
  • gene : n. 【生物學】基因。 dominant gene顯性基因。
  • product : n. 1. 產物，產品；製品；產量；出產。2. 結果，成果。3. 創作，作品。4. 【化學】生成物；【數學】積，乘積。
  1. Prokaryotic expression of vp2 gene of infectious bursal disease virus and antigenicity of expressed product

    2基因的原核表達與抗原性分析
  2. Screening target ' gene of artemisinin antimalarials using drug - western from cdna expressing library : 12 b - deoxoartemisinyl - ( 4 ' - oxyacetic acid ) phenyl ether was linked to bsa by using of edc cross ! inker and the product acted as drug - probe

    對重組pmd一18一t克隆載體及pqe一30表達載體雙酶切，提取tctp基因和pqe一30空載體並使二者重組，然後轉化m15 ，挑取陽
  3. Considering of the specificity of the degenerative primer designed in this pcr reaction, the identity between the sequence we wanted and the fragment of pcr product and the presence of asmaspa, asmaspb, clr and cls ( the homologous gene of masp gene ) in halocynthia roretzi, a japanese ascidian, we believe that the sequence of pcr product is some part of the masp gene or masp homologous gene

    基於本實驗中所設計的引物為特異性簡並引物，測序基因通過比較得到與預期片段有一定的同源性以及masp同源物asmaspa 、 asmaspb 、 clr和cls在海鞘中存在的事實，我們可以初步推測，本實驗pcr反應所克隆的片段可能為文昌魚masp或其同源基因的一部分序列。
  4. In this study, iltv - nm98a strain and iltv - wanggang strain were multiplied in chorioallantois. a pair of primers were devised according to the nucleic acid sequence of iltv tk gene and the dna of multiplied virus was used as pattern to amplify the gene of tk by polymerase chain reaction ( pcr ). the product of pcr was linked with suitable plasmid. then, the recombined plasmid was converted to escherichia coli. the converted escherichia coli

    根據已發表的iltvtk基因的核苷酸序列設計一對pcr引物，以增殖的兩株iltv的dna為模板，分別對它們的tk基因進行pcr擴增。將回收的pcr產物連接到適當的質粒載體上，轉化感受態大腸桿菌，通過篩選對iltvtk基因的陽性克隆進行擴增培養。
  5. These results show that coda gene cloned from e. coli can express specifically in the anther of both monocotyledon and dicotyledon plant species upon induction of 5 - fc, and the in vivo expression product of the gene can transform the 5 - fc used externally into 5 - fu, which leads to all or partial inactivity of anthers and / or pollens

    以上結果表明， coda基因在單子葉植物和雙子葉植物花藥中的特異性表達，能將外用的5 - fc在體內轉化為5 - fu ，導致花藥或花粉的部分和全部失活。
  6. According to these problems, we adopt to the method of mending material, optimize to fermentation media and partly ferment condition. finally, we excogitate a kind of fermentation technology that is suitable for target gene efficiency expressed and is advantageous of product purified. with the plasmid pbv220 - ifnr, pbv220 - hgfa, pbv220 - hgfb, pbv220 - hpk5 that expresses serve as the model, adopting the biostat - c15l of b. braun company, utilize the method of mending material to ferment, through optimization fermentation media and optimization partly ferment condition ( ventilate quantity, stir speed, mend material speed ), eventually establishment a kind of fermentation technology that is suitable for target gene efficiency expressed and is advantageous of product purified

    以我室構建並穩定表達的重組質粒pbv220 - - ifn 、 pbv220 - hgf 、 pbv220 - hgf 、 pbv220 - hpk5為模型，分別從不同的表達宿主菌中篩選出一種適合大規模生產的菌種bl21 （ de3 ） ，該工程菌株連續傳代100代表達質粒不丟失，表達量穩定；採用b . braun公司的biostat - c15l自控發酵罐，運用分批補料技術分別進行四種工程菌的高密度發酵，通過優化工程菌發酵的培養基配方及優化部分發酵條件（通氣量、攪拌速度、補料速度） ，最終建立一種適于目的基因高效表達的高密度發酵工藝模式。
  7. With the successful expression of exogenous gene in plant. the advantage of plant expression system become a highlight increasingly. based on the successful expression of hbmp - 3m gene into tobacco, we maked the study o f transferring hbmp - 3m gene into tomato and hbmp - 3 gene into tobacco, in order to obtain tomato transgenic plant with hbmp - 3m gene and tobacco transgenic plant with hbmp - 3 gene, to establish basis for getting step farther of leaning the expression of hbmp - 3m gene and hbmp - 3 gene in plant, the difference between the product of hbmp - 3m gene and hbmp - 3 gene in plant and the active of expressible product

    隨著植物基因工程的迅猛發展，一些疫苗、抗體、細胞因子等異源蛋白在植物中的成功表達，植物表達系統的優點日益受到關注。本研究室在成功地將hbmp - 3成熟肽基因轉入煙草並檢測有目的蛋白表達的基礎上，進行hbmp - 3成熟肽基因轉化番茄和hbmp - 3全長基因轉化煙草的研究，以期獲得轉hbmp - 3成熟肽基因番茄和轉hbmp - 3全長基因煙草植株，為進一步研究hbmp - 3成熟肽基因和全長基因在植物體內的表達及區別奠定基礎。
  8. Cluster analysis based on rapd showed that at 76 % similarity level, all tested isolated could be clusted into nine groups, i. e. 1 p. ostreatus and p. florida, ii p. ostreatm p. sapidus, p. spodoleucus and p. eryngii, iii p. colnmbinus, p. corlicalus, p. cornucopiae, p. nebrodensis and p. ferulae ; iv p. pulmonarius and p. sajor - caju, v three isolates with indefinite species, vi p. luber - regium, vii p. cilrinopileatus, viii p. djamor and p. salmoneoslramincus, ix p. abalonus and p. cysliodism. 4. a single uniform product 1. 46kb in size resulted from pcr amplification of the 5 " half of the 28s rrna gene for all isolates of pleurolus and the other three genera

    隨機擴增多態性dna的聚類分析表明，在76相似水平下，可將供試的側耳菌株聚成九大類，第一大類包括糙皮側耳、佛羅里達側耳；第二大類包括美味側耳、灰白側耳、剌芹側耳；第三大類包括哥倫比亞側耳、裂皮側耳、黃白側耳、阿魏蘑、白阿魏蘑；第四大類包括肺形側耳和鳳尾菇；第五大類為3株未定名的側耳；第六大類僅有具核側耳；第七大類為金頂側耳；第八大類包括紅平菇和桃紅側耳；第九大類包括鮑魚菇和囊蓋側耳。
  9. Expression of thermostable direct hemolysin gene of vibrio parahaemolyticus in e. coli and activity of expressed product

    副溶血性弧菌直接溶血毒素基因的原核表達及產物的性質
  10. Porcine transmissible gastroenteristis is an importan contagious disease endangering the development of swine. in other to establish a rapid diagnosis method and provide effective immunogenic products, the nucleoprotein ( n ) gene of porcine transmissible gastroenteristis virus ( tgev ) was cloned. expressed and its expressed product was purified

    為建立對豬傳染性胃腸炎快速有效的診斷方法，並試圖在預防上提供有效的免疫制劑，本論文首次在我國對豬傳染性胃腸炎病毒核衣殼蛋白基因進行了克隆、鑒定、表達及重組核蛋白的純化；並在細胞上對重組核衣殼蛋白抗體的中和效力進行了測定。
  11. Reclamation, purification and linkage of them respectively, then sequencing and analyses of according gene structure were made, results show that the complete sequence length of corresponding pcr product from brussel sprouts, kohlrabi and kale are 1665bp, 1650bp and 1650bp, containing the first two exons and introns and 22bp of the third exon

    對各pcr產物分別進行回收、純化、載體連接和序列測定及基因結構分析等，結果表明，該片段在抱子甘藍、羽衣甘藍和球莖甘藍三種作物中的全長分別為1665bp 、 1650bp和1650bp ，包括相應基因的前兩個外顯子和內含子以及第三個外顯子的22bp序列。
  12. Operon is a unit of bacterial gene expression and regulation, including structural genes and cis - acting control elements in dna recognized by regulator gene product ( s )

    控制某一代謝途徑的相關基因，緊密連鎖地排列在一起，受同一操縱子控制。
  13. The expression of nm23 gene product and its relationship with inva - sion and metastasis of colorectal carcinoma

    1蛋白在大腸癌患者中表達的臨床意義
  14. Howeer, protein gene product 9. 5 - immunoreactie fibers were obsered in scar tissues on the surface of the puncture site

    但是，在穿刺處表面，我們找到了9 . 5蛋白基因產物的免疫反應纖維。
  15. In our study we have cloned the osd gene from s. typhimurium by pcr, characterized the gene product and used this gene to construct asd + expression cloning vectors ptrc99a - asd

    再將hpylori尿素酶b亞單位基因與尿素酶b和熱休克蛋白a融合基因分別克隆入ptrc99a一asd質粒的多克隆位點之內。
  16. In all the discs, including nonpunctured control discs, protein gene product 9. 5 - immunoreactie fibers were only occasionally obsered in the outermost part of the anulus fibrosus

    在包括未穿刺的對造組在內的所有椎間盤中， 9 . 5蛋白基因產物的免疫反應纖維只是偶爾在環狀纖維的最外邊被觀察到。
  17. To civilianize the gene product is an important development direction for genomic industry. besides the research on genomic technology itself, research on the innovation and preemptive working strategy for civilian genomic product has great importance as well

    基因產品的民用化是基因產業發展的重要方向，除了對基因技術進行創新研究，基因民用化產品在營銷方面的創新性、前瞻性的研究理所當然地也具有十分重要的意義。
  18. Green fluorescent protein is widely applied in researches of modern life science, such as gene product moved - process in vivo, protein localization, drug screening and preliminary selection of transgenic individual as a molecular marker

    綠色熒光蛋白這種獨特的生物學特性，使其作為報道基因在現代生命科學研究領域中，如細胞內基因產物的動態過程，蛋白質在細胞內的定位，藥物的篩選，以及轉基因個體的初步鑒定等等有著廣泛的應用。
  19. Two types of repeat sequence, a 15 - amino - acid ( eelcaqlcstppppi ) with 2 repeats and a 6 - amino - acid ( ppictp ) with 4 repeats, were firstly reported. 2. the characterization of meq gene product and its expression within the cells a recombinant baculovirus transfer vector pblubac4 - meq was constructed by cloning meq gene of marek ' s disease virus ( mdv ) ga strain into the baculovirus transfer vector pbluebac4 under the polyhedrin promoter

    此外，研究還發現了meq基因的兩類有趣的重復結構，其中一類是含15個氨基酸殘基（ eelcaqlcstppppi ）的結構，有2個重復，另一類是含6個氨基酸殘基（ ppictp ）的結構，共有4個重復，它們全部分佈在meq蛋白c -端的轉錄激活域內。
  20. The absence of the fmr1 gene product, fragile x mental retardation protein ( fmrp ), is believed to be responsible for the typical physical and mental characteristics of the fragile x syndrome. alleles with between 43 and 200 cgg repeats are called permutation. they are generally unmethylated with normal transcript and protein level, but are extremely unstable during transmission to next generation

    帶有前突變（ n = 43 200 ）的個體其fmr1基因通常不會甲基化，可以正常轉錄和翻譯產生fmrp ，故沒有臨床表型出現，但是，在向下一代傳遞的過程中卻是非常不穩定的，會從前突變擴增成為全突變。
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