genetic vaccine 中文意思是什麼

genetic vaccine 解釋
基因疫苗
  • genetic : adj. 1. 遺傳（學）上的。2. 發生的，發展的；創始的。adv. -ically
  • vaccine : adj. 牛痘的；預防疫苗的；種痘的。n. 1. 疫苗，牛痘苗；菌苗。2. 【計算機】免疫程序軟體，抗病毒軟體。
  1. Immunotherapy for swine cysticercosis with the genetic engineering vaccine

    豬囊尾蚴細胞疫苗的區域試驗研究
  2. Somatostatin is a neurohormone which p1ay mu1tilatera1 physio1ogic function in vertebra animal body ( including human ), to study ss genetic engineering vaccine is of great significance and have extensive appl ication potent ial

    生長抑制因子（ somatostatin ， ss ）是脊椎動物（包括人）機體中具有多種生理功能的神經激素。研究ss基因工程疫苗既具有理論意義，又有廣泛的應用前景。
  3. A novel dynamic evolutionary clustering algorithm ( deca ) is proposed in this paper to overcome the shortcomings of fuzzy modeling method based on general clustering algorithms that fuzzy rule number should be determined beforehand. deca searches for the optimal cluster number by using the improved genetic techniques to optimize string lengths of chromosomes ; at the same time, the convergence of clustering center parameters is expedited with the help of fuzzy c - means ( fcm ) algorithm. moreover, by introducing memory function and vaccine inoculation mechanism of immune system, at the same time, deca can converge to the optimal solution rapidly and stably. the proper fuzzy rule number and exact premise parameters are obtained simultaneously when using this efficient deca to identify fuzzy models. the effectiveness of the proposed fuzzy modeling method based on deca is demonstrated by simulation examples, and the accurate non - linear fuzzy models can be obtained when the method is applied to the thermal processes

    針對模糊聚類演算法不適應復雜環境的問題，提出了一種新的動態進化聚類演算法，克服了傳統模糊聚類建模演算法須事先確定規則數的缺陷.通過改進的遺傳策略來優化染色體長度，實現對聚類個數進行全局尋優;利用fcm演算法加快聚類中心參數的收斂;並引入免疫系統的記憶功能和疫苗接種機理，使演算法能快速穩定地收斂到最優解.利用這種高效的動態聚類演算法辨識模糊模型，可同時得到合適的模糊規則數和準確的前提參數，將其應用於控制過程可獲得高精度的非線性模糊模型
  4. Field study of immunization against swine cysticercosis with the genetic engineering vaccine in an endemic area in china

    豬囊蟲病基因工程疫苗用於免疫治療的研究
  5. Research progress of molecular biology and genetic engineering vaccine of enterotoxic escherichia coli

    腸產毒性大腸桿菌分子生物學及基因工程疫苗的研究進展
  6. Because of gpv highly contagious, new genetic engineering vaccine and a rapid, special and simple diagnosis method is required to prevent and detect the infection

    由於本病傳播快、致死率高，開發研製新型的基因工程疫苗以及建立一種快速、簡便、特異的診斷方法非常必要。
  7. The results in this experiment are very important for further study on development of genetic engineering vaccine against rabies and on the investigation of molecular epidemiology of rabies virus

    實驗結果對狂犬病的分子流行病學、致病機理的研究及基因工程疫苗開發是十分重要的。
  8. This study provides the basis evidence and material basis for prv identification molecular epdiemiology investigation, research of diagnostic reagent and genetic engineering vaccine

    本研究為國內prv毒株鑒定、分子流行病學調查、分子診斷試劑的開發以及基因工程疫苗的研製提供了理論依據和物質基礎。
  9. Living vaccine and killed vaccine have some formidable drawback, so biological technology vaccine, for example, gene vaccine and genetic engineering vaccine, is under the circumstances

    現在使用的弱毒苗和滅活苗都存在著一些難以克服的缺點，基因免疫和基因工程疫苗等生物技術疫苗的研製已勢在必行。
  10. In this study, the recombinant fowl - poxvirus was transfected into expressing the vp3 gene of isolated gpv h1 strain into the cef cells with fpv - 017 by liposome, which have the lacz reporter gene, earlier / latter promoters lp2ep2 of fpv, promoters p7. 5 and p7. 1 of vaccinia virus, replication unnecessary region of fpv - 017. following 6 cycles screenings, clonings, purification of blue plaques, detection of pcr and dot - elisa, which verified the genetic stable vp3 - fowlpox virus recombinant constructed successfully. this study provided the theoretical and practical foundation for development of gpv recombinant fowl - poxvirus genetic engineering vaccine, as well as provided substance preparatory for prevention the high mortality gpv

    本研究採用脂質體轉染方法，將含有完整gpvh1分離株vp3基因、報告基因lacz 、禽痘病毒早晚期啟動子lp2ep2 、痘苗病毒啟動子p7 . 5 、 p11和fpv - 017復制非必須區的轉移載體質粒psy681vp3lacz與fpv - 017共轉染雞胚成纖維細胞，經6輪蝕斑克隆、篩選、表達， pcr鑒定和dot - elisa檢測，證明該重組病毒已構建成功，並獲得了遺傳性狀穩定的鵝細小病毒vp3基因的重組禽痘病毒。
  11. Vp3 gene of hl isolate of goose parvovirus derived from recombinant piasmid pproex htb - vp3 was subcloned into ecorl site of psy538, and the reporter gene lacz with promoter pll was cloned into smai site of recombinant piasmid. both vp3 gene and lacz gene were cloned into noti site of psy681, recombinan fpv transfer vector containing vp3 gene of gpv was obtained. the result is basis of construction of recombinant fpv expressing vp3 gene of gpv and gpv genetic engineering vaccine

    本研究另從含有gpvh1分離株主要結構蛋白vp3基因的重組質粒pproexhtb - vp3中切取gpvh1株vp3基因片段，將其亞克隆于psy538的ecori位點，然後將帶有痘苗病毒啟動子p11的lacz報告基因平端克隆于上述重組子的smai位點，再用noti切下同時含有vp3基因和lacz報告基因的片段，再亞克隆于psy681的noti位點，構建出含有vp3基因的重組禽痘病毒轉移載體，為構建表達vp3基因的重組禽痘病毒從而制備gpv基因工程疫苗奠定了基礎。
  12. Another project underway is the use of genetic engineering techniques to develop a vaccine for some diseases

    正在進行的另一個項目是利用遺傳工程技術研製某些疾病的疫苗。
  13. Two strains of prrsv were isolated from the swine infected with prrsv in shangdong province and daqing area, in order to clarify the source and genetic background of porcine reproductive and respiratory syndrome virus ( prrsv ) from different parts of china, thus providing theoretic basis for the study of vaccine against it. the prrsv was cultured on mark - 145 cells for 5 ~ ~ 6 passages. when the cpe was obvious, the virus was harvested and purified

    為了弄清我國不同地區prrsv的來源以及其遺傳學背景，為疫苗學研究提供理論根據，本研究在ch - 1a株完整的基因組獲得以後，從流行於我國山東（ sd ）和黑龍江大慶（ dq ）地區疑似prrs的豬體內分離到prrsv ，在mark - 145細胞上盲傳5 6代，細胞出現明顯病變以後，收獲病毒液，然後提純，提取全病毒rna ，經過反轉錄、 pcr擴增獲得結構基因orf2 7的目的基因片斷，然後與pmd - t載體連接，轉化，得到陽性質粒后進行測序，並將其與ch - 1a株進行了比較分析，同時對這兩個毒株的結構基因組的理化性質進行分析。
  14. Genetic vaccine is quite different in structure from traditional ones. the experiments show that delivery of genetic material into an animal ' s cells can trigger some synthesiztion of the encoden proteins as well as of antibodies targeted against those proteins

    核酸疫苗是將編碼某種抗原蛋白的外源基因插入某種表達載體中並直接導入的動物體內，表達抗原蛋白，並誘導宿主產生對該抗原蛋白免疫應答的革命性的新型疫苗。
  15. This study provides the basis evidence for the research of nucleotide sequence evolution relationship between domestic and exterior countries. it also establishes foundation for further research about developing gpv molecular diagnostic reagent and genetic engineering vaccine

    本研究為了解國內外鵝細小病毒核苷酸序列演化上的關系，為開發研製新型分子診斷試劑和抗鵝細小病毒感染的基因工程疫苗提供了理論依據。
  16. The influence of cellular immunity and genetic factor on the effect of mother to infant transmission interrupted with hepatitis b vaccine

    6融合基因在恥垢分枝桿菌中的表達及其抗原性的初步研究
  17. Prevention and cure of the derzsy ' s disease depended on vaccine and antiserum, antibodies of eggs. the vaccines includes goose embryo and duck embryo vaccines which were used 1n breed goose and goslings, and those vaccines have great effect in breeding goose, but the entire virion live vaccines and attenuated vaccines exist many deficiencies. such as preclinical infection, dissemination of virus, recovery of viru5, etc. those proplems can be sol / ed by producing genetic engineering " asclne

    目前使用的疫苗分為種鵝用和雛鵝用的鵝胚和鴨胚化疫苗，這些疫苗在實際生產中發揮巨大作用，因其為全毒苗或弱毒苗，存在著潛伏感染，排毒散毒，毒力返祖的缺陷，基因工程疫苗的研製可解決上述問題。
  18. Caenorhabditis elegans, a kind of free - living nematodes, has been used as study of genetic function of parasitic nematodes and as expression of the potential vaccine antigens of important parasitic nematodes

    摘要秀麗隱桿線蟲作為一種模式線蟲，已廣泛應用於寄生性線蟲基因功能的研究以及寄生性線蟲疫苗候選抗原基因的表達。
  19. It has made the strong basis for further studying mechanism of replication, virulence and determinant, attenuation, pathogenesis, functions of genetic products, specific diagnosis, cell and host tropism, development of dna vaccine and marker vaccine of csfv, and provided an excellent tool for molecular virology. main research contents include : based on published nucleotide sequences of csfv and by the help of computer analysis software, high conservative regions and single restriction enzyme sites of genome were selected. utilizing rt - pcr and nested - pcr techniques, 7 overlapping cdna fragments covering the full genome of csfv c - strain were successfully amplified

    中國豬瘟兔化毒（脾淋毒）基因組cdna文庫的構建、序列分析：根據已發表的豬瘟病毒（ csfv ）核苷酸序列，藉助計算機軟體分析，選擇高保守區段和基因組中的單一限制性酶切位點，利用rt - pcr及nested - pcr和helf - nestedpcr技術，成功地擴增出了覆蓋c -株全基因組的7個cdna重疊片段f1 f7 ，分別克隆到pmd - 18t或pgem - teasy載體進行測序后，拼接出了其核苷酸序列。
  20. In order to study immunization of genetic vaccine by inoculation, two kinds of dna vaccine of ndv are constructed and analysed their sequense, which will express f protein in eukaryotic cell ( hela cell ) in vitro with the method of transfection by cationic liposome the results testify that two sorts of plasmids dna successfully expressed the f protein of ndv in hela cell, but the expressed content of pc4. 0f is higher than ones of pc3. 1f

    將構建的基因疫苗pc3 . 1f大量提取和純化，採取肌肉注射和腹腔注射兩種途徑、不同劑量免疫小鼠，用elisa方法檢測小鼠血清中抗f基因表達產物的抗體水平。研究結果表明，基因疫苗pc4 . 0f和pc3 . 1f均在hela細胞中成功表達，其中pc4 . 0f的表達量比pc3 . 1f高。
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