coat protein 中文意思是什麼

coat protein 解釋
病毒蛋白外殼
  • coat : n 1 上衣，外衣，外套。 ★厚大衣叫 overcoat 〈英國〉 greatcoat 2 （女人、孩童的）短大衣。3 鎖子甲。...
  • protein : n. 【化學】朊，蛋白（質）。
  1. Overexpression of sweet potato feathery mottle virus coat protein in e. coli and preparation of its specific antiserum

    甘薯羽狀斑駁病毒外殼蛋白基因在大腸桿菌中的表達及特異抗血清的制備
  2. E. coli xl1 - blue cells were tansformed by psurfpga and phages were rescued by m13ko7 helper phage particles. results showed that the heterodimeric enzyme was expressed as a fusion protein that matures to an active biocatalyst connected to the coat protein of phage fd

    以構建的噬菌粒psurfpga轉化具有琥珀突變的大腸桿菌xl1 - blue ，以輔助噬菌體m13k07超感染，進行青霉素g酰化酶基因的表達和在噬菌體表面的展示。
  3. Capsid the protein coat of a virus, which surrounds its nucleic acid

    衣殼：病毒的外殼蛋白，包圍著核酸。
  4. It was thought earlier that multiple copies of no more than a few different proteins make up the protein "coat" of the ribosome.

    人們以前認為組成核蛋白體蛋白質「外殼」的只不過是幾個不同蛋白質的重復拷貝。
  5. Like the trypanosome ' s vsg coat, the immune system ' s b lymphocytes also express one protein ( immunoglobulin ) on their surface at a time, even though each b cell has many different genes for the surface proteins

    一如錐蟲的vsg外套，人體免疫系統的b淋巴球就算擁有許多不同表面蛋白的基因，每回也只表現一種表面蛋白（免疫球蛋白） 。
  6. A virion consists of a protein coat surrounding one or more strands of dna or rna

    一個病毒粒子包括外部的蛋白衣殼和內部的一條至多條dna或rna鏈。
  7. High - level expression of bydv gav coat protein gene in escherichia coli

    株系外殼蛋白基因在大腸桿菌中的高效表達
  8. Cloning of potato virus s coat protein gene and its expression in e. coli jm

    病毒外殼蛋白基因的克隆及其在大腸桿菌中的表達
  9. Construction and transformation of inverted repeat of turnip mosaic virus coat protein gene

    基因反向重復植物表達載體的構建及遺傳轉化
  10. Expression of apple chlorotic leaf spot virus coat protein gene in e. coli

    蘋果褪綠葉斑病毒庫爾勒香梨分離物外殼蛋白基因在大腸桿菌中的表達
  11. To guide the cam - binding peptide into apoplast space, the signal peptide from brassica campetris pollen coat protein slr1 ? ps was employed. it has total 26 amino acid, and is a very classic form of signal peptide

    為了把cam結合小肽帶到質外體，本實驗選擇了野生蕓苔屬植物（ brassicacampetris ）花粉胞壁蛋白slr1 - bps的信號肽。
  12. Phage display describes a selection technique in which a peptide or protein is expressed as a fussion with a coat protein of bacteriophage, resulting in display of the fused protein on the surface of the virion, while the dna encoding the fussion resides within the virion

    自1985年gpsmith首次提出噬菌體展示技術以來，隨著生物技術的發展，噬菌體隨機肽庫已成為研究分子間相互作用的有力工具，特別是在抗原表位研究方面。
  13. Meanwhile, these six coat protein genes were sequenced and compared with other homologous sequences in genbank. the strain designation of the six isolates of tumv was finally determined. the results are as the following : 1. six isolates of turnip mosaic virus named tumv - sd1, tumv - sd2, tumv - sd3, tumv - sd4, tumv - sd5 and tumv - sd6 were respectively acquired from infected chinese cabbages and radishes in 3 cities ( taian, yantai and zaozhuang ) of shandong province

    利用rt - pcr方法克隆了tumv山東分離物的外殼蛋白（ cp ）基因，測定了它們的核苷酸序列、並將其與已報道的序列進行同源性比較和分析，最終確定了其歸屬地位，具體研究結果如下： 1 .從山東省3地市感病的白菜和蘿卜上分離到蕪菁花葉病毒的6個分離物，分別命名為tumv - sd1 、 tumv - sd2 、 tumv - sd3 、 tumv - sd4 、 tumv - sd5和tumv - sd6 。
  14. 2. an up - dated method was employed to purify tumv in this research. using the protease k method, we acquired the viral genome - rna. a pair of specific primers was designed and synthesized based on the nucleotide sequences of tumv coat protein genes reported before and rt - pcr was used to clone the cp genes of the six tumv isolates

    應用改進的蕪菁花葉病毒的提取方法從病葉中提取病毒粒體，應用蛋白酶k法從病毒粒體中提取病毒rna基因組，根據已報道的tumv的cp基因序列，設計併合成了一對特異引物，利用rt - pcr法克隆了6個分離物的外殼蛋白基因，與克隆載體puc19連接后通過熱激法轉化大腸桿菌dh5 。
  15. Exposure of certain viruses to low ionic strength results in subtle changes in the protein coat.

    某些病置於低離子強度的環境中，可引起蛋白質外殼的細微改變。
  16. Thin sections of host leaf cells infected by bbwv - 2 isolate b935, which were gold - labeled by antibodies of bbwv - 2 coat protein ( cp ) and vp37, respectively, were prepared to elucidate the locations of vp37 in cell and possible function of vp37 and cp in cell to cell movement. observation in electron microscope showed that virus particles were presented not only in cytoplasma but also in chloroplast, while vp37 was existed only in cytoplasma and associated with tubular structure through the cell wall

    為研究vp37在寄主細胞中的作用機制及其在細胞中的分佈，通過膠體金間接標記6his - vp37兔抗血清，同時還標記了病毒的外殼蛋白單克隆抗體，對bbwv - 2分離物b935感染的病葉超薄切片的電子顯微鏡觀察發現：病毒粒子除了聚集在胞質中，還存在於寄主的葉綠體內； vp37蛋白能在細胞壁上形成管狀結構，在胞質中亦有分佈。
  17. The detection of coat proteins in host chloroplasts infected with tumv the intact chloroplasts were isolated, the proteins attached to the chloroplast surfaces digested, then the total proteins of chloroplasts extracted. the coat protein was detected in both chloroplasts of chinese cabbage and mustard infected with tumv through western blot

    寄主葉綠體中tumv外殼蛋白的檢測通過提取青菜和芥菜葉片中的完整葉綠體，用胰蛋白酶消除其表面蛋白后，抽提葉綠體總蛋白，然後用westernblot檢測，證明ti1mh cp存在於感病寄主的葉綠體中。
  18. Different hosts " response suggested that tumv - sd1 could infect plants of 10 species in 3 families. tumv - sd1 formed pine - wheel inclusion bodies in plant cells. the coat protein of the tumv - sd1 contains 3 components whose estimated molecular weight are 45kd, 38kd and 14kd respectively

    寄主反應特性表明， tumv - sd1 6能侵染3科10種植物， tumv - sd1在寄主細胞內形成風輪狀內含體，外殼蛋白為3組分，分子量分別為45kd 、 38kd和14kd ；提純的病毒粒體為長線條狀。
  19. A polypeptide with sequence of qkvdssggggs was designed to be a linker between c terminal of penicillin g acylase and n terminal of the coat protein. the ribosome binding site ( rbs sequence ) of psurfscript is also replaced by rbs sequence originating from bacillus subtilis. it was demonstrated that constructed phagemid can still express penicillin g acylase

    將包含信號肽和琥珀終止密碼子uag （ amber ）的完整巨大芽孢桿菌青霉素g酰化酶基因克隆到噬菌粒psurfscript ，通過引入的11肽連接青霉素g酰化酶的c末端與噬菌體外殼蛋白gp3的n末端。
  20. On the other hand, maize dwarf mosaic ( mdm ) is a kind of main disease that cause huge drop in production and there is no effective pesticide now. antisense rna of maize dwarf mosaic virus coat protein ( mdmv - cp ) gene can well depress the assemble of coat protein, avoiding mdmv disease effectively

    玉米矮花葉病是造成玉米減產的一種重要病毒病害，目前尚無有效的化學藥物加以防治，而利用反義rna技術培育抗玉米矮花葉病的轉基因玉米是一條防治玉米矮花葉病害的經濟、有效的途徑。
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