dna virus 中文意思是什麼

dna virus 解釋
dna簿
  • dna : 1. deoxyribonucleic acid 【生物化學】去[脫]氧核糖核酸。2. deoxypentose-nucleic acid 去[脫]氧戊糖核酸。
  • virus : n 1 【醫學】病毒；濾過性病原體。2 毒素；毒害。3 惡意，惡毒。4 【計算機】（電腦）病毒〈指擾亂或破...
  1. 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。
  2. The characteristics of tm - 22 expression presented in transgenic tobacco : 1 ). virus specificity in either homozygote or heterozygote ; 2 ) tm - 22 gene integrated in tobacco genomic dna with single copy and in inheritance and segregation to progenies on the mendel role ; 3 ). transgenic line with tm - 22 promoter ( ptm47 ) showed infected symptoms with cell death distinguished to one with 35s promoter ( ptm49 ) after inoculation with tomv - 2a

    其次，通過氨基酸序列和結構的比較，確定tm - 2 ~ 2基因的編碼蛋白與tomv病毒在抗病反應中相互識別的特異氨基酸及其功能；然後，應用重組dna技術，互換tm - 2 ~ 2基因和tm - 2基因的對應結構域，構建嵌合基因，獲得嵌合蛋白表達的轉化體，驗證tm - 2 ~ 2編碼蛋白中變異氨基酸的作用。
  3. An establishment gram institute contains " the k factor " to be able to produce the strong effect immune body, suppression virus activeness, causes viral dna to be unable to duplicate, routs the cause of disease parent substance at one fell swoop, causes the virus to burst the death, never recurs

    安立克kj劑"系列藥物排出的病毒主要聚集在這個部位。安立克所含的「 k因子」能產生強效的抗體，抑制病毒活性，使病毒dna無法復制，一舉擊潰病原母體，使病毒破裂死亡，永不復發！
  4. We immunize the balb / c mice with pc4. 0f and pc3. 1f by paunch and muscle administration and immunize each with different content of 10 g, 50 g 100 g. the antibodies in serum against newscastle disease virus f gene protein are tested by elisa. the result showes that two kinds of dna vaccines can induce specific antibody response to encoded proteins in 15 weeks by im and ip, but antibodies response is little different

    免疫結果顯示，採用2種免疫途徑（肌肉注射，腹腔注射） ， 3個劑量（ 10 g 、 50 g和100 g ）免疫balb c小鼠，在被檢測的15周內，肌肉注射和腹腔注射組均可產生抗體，抗體的產生有明顯的劑量依賴性， 50 g只和100 g只明顯優於10 g只，而100 g只與50 g只相似（肌肉注射）甚至稍低（腹腔注射） 。
  5. By using aa 385 - 365 fragment, an elisa system for the evaluation of post - e2 - vaccination humoral immune responses was also established, and was successfully applied to recombinant vaccinia virus - and dna - based vaccine research

    利用aa385 - 565片段，建立了e2疫苗免疫后抗體反應的elisa評價體系，並已成功用於重組痘苗病毒疫苗和dna疫苗的研究。
  6. Two plasmids, which contain hbv specific dna fragment and hsv1 dna fragment, were amplified by solid phase two loci pcr and detected by enzymatic indicator system on a gene chip that was constructed by primer immobilization and modified with thiol group on chip surface. for building detection technology by dna chip in clinical, the virus genomes were extracted from the clinical positive samples by one - step nucleic acid extraction

    採用已建立的晶元制備方法，在該六種質粒中選擇含有hbv與hsv1兩種病毒dna序列的質粒為模板，進行同相兩重pcr ，採用晶元酶學槍測對固相兩重pcr的擴增結果進行檢測，得到良好的晶元酶學檢測結果。
  7. The env protein deduced from env gene encodes the hydrophilic surface protein ( su ) and the hydrophobic transmembrane domain ( tm ) that determine the specific interaction between virus particles and cell surface receptors during retroviral entry. the su of retroviruses is a highly variable genetic element, containing receptor binding sites and major antigenic determinants. exjsrv - specific dna probes were derived. by using these dna probes in tissue hybridization. we successfully identified jsrv mrna expression and proviruses dna in sheep lung tissues infected with jsrv and control group has no postive signals, validating the use of exogenous virus - specific dna probes in the analysis of oncogenic proviral integration sites and identification of integrated exogenous proviral sequences

    用地高辛隨機引物法標記exjsrv特異的env片段，制備探針，原位雜交檢測spa肺組織中的rna及前病毒dna ，結果表明spa患羊肺組織內有jsrvenv基因mrna的表達，同時也檢測到了前病毒dna ，而相應的陰性對照卻無陽性信號，證實外源性病毒特異的dna探針在致瘤性前病毒的整合位點和整合的外源性前病毒的檢測中具有可信度。
  8. Cell immune response induced by hepatitis b virus dna vaccine in mice

    乙肝病毒核酸疫苗誘導小鼠細胞免疫應答的研究
  9. The homology of recombinant virus bmpak - hbmp was obtained and identified by plaque assay and baculovirus contains the hbmp gene was confirmed through pcr and dna dot blotting. the expressed rhbsag was determined by elisa after infecting bm - n cells and pupae with recombinant virus bmpak - hbmp and bmpak - hbm ( containing nonfusion hbv surface antigen medium sized )

    用重組病毒bmpak - hbmp和bmpak - hbm [帶有非融合乙肝表面抗原（ pres2 + s ）基因，為本實驗構建]感染家蠶細胞及蛹，對兩種病毒的表達產物用elisa進行了跟蹤檢測，結果表明，感染bmpak - hbmp的家蠶細胞及蛹中rhbsag的表達量分別為3
  10. The changes of above show that the damage to the chicken embryo caused by the chicken parvoviruses were widly. the pathogeny of infectious stunting syndrom was prolifirated in cells nucleus, it was a dna virus

    以上變化說明了分離病毒對機體損傷的廣泛性。核內包涵體的出現進一步說明，雞傳染性生長障礙綜合征的病原在細胞核內增殖，為dna病毒。
  11. The pbacph - egf plasmid dna was used to co - transfect bmn cell with the modified bombyx mori baculovirus bm - bacpak dna, which was first linearized by aocl. after two rounds of plaque isolation, the recombinant virus ( named bmbacph - egf ) was further verified with pcr and dot hybridization. the recombinant bmbacph - egf virus was used to infect bmn culture cells at a moi of 10

    重組轉移載體dna與經bsu36i酶切線性化的修飾型病毒bm - bacpakdna共轉染家蠶bmn細胞，兩輪空斑篩選和純化，獲得重組病毒rbmbacph - egf ，經pcr擴增、 dna點雜交等方法鑒定證實重組病毒中已正確插入ph - egf融合基因。
  12. The angiostatin baculovirus transfer vector was co - transfected with viral dna into sf9 cells according to the manufacturers protocol. to purify the recombinant virus, we used the plaque assay to screen the pure recombinant plaque and amplify it to generate p - 1 stock

    構建重組病毒：用已經構建好的angiostatin桿狀病毒轉移載體pbluebachiszb和病毒dna共同轉染sfg細胞，通過蝕斑實驗篩選出純的重組斑點並擴增產生p二病毒貯存液。
  13. Finally, a tranfer vector named as pltk - ha was constructed based on pltk - uni with insertion of ha gene of h3 subtype srv. the pltk - ha and prv bartha - k61 genomic dna were co - transfected into 50 - 70 % confluent vero cells in 6 - cm dishes. based on the expression of lacz gene, recombinant prv were selected and purified by blue - colored virus plaque

    利用脂質體介導的方法，將pltk - ha與prvbartha - k61基因組共轉染于亞單層vero細胞，依據報告基因lacz在細胞中的表達，篩選藍色蝕斑的重組病毒，經數次蝕斑純化后， pcr鑒定、 western - blot分析。
  14. After one - step reverse transcription of the rna virus genomes, the viruses " specific dna fragments were amplified by nested three loci pcr, which the amplification system was optimized by uniform design

    選擇合適的核酸抽提方法，一步法抽提hbv 、 hcv及hiv 1的病毒核酸並一步法逆轉錄病毒的rna ，獲得病毒的dna 。
  15. Successfully cloned and constructed infectious full - length cdna of attenuated lapinized csfv chinese - strain ( derived from spleen ) could make us get pure rna virus genome of csfv c - strain, and further study and utilize mutation, deletion, insertion and substitution of csfv gene on dna molecular level

    中國豬瘟兔化弱毒（脾淋毒）全長感染性cdna的克隆和構建，可以使我們得到純粹的csfvc -株rna病毒基因組，在dna水平上研究和利用csfv的基因突變、缺失、插入和替換。
  16. Was obvious to all to be detailed the establishment gram venereal diseases kj medicinal preparation is one high active living thing medium which in the outside too bareness oxygen, the low attraction, under the high radiation special environment in the middle of the copy process has the completely block the viral dna duplication, skin base first floor and the dermis cellular layer comprehensively sweeps clean the virus

    Annlic安立克kj劑是在外太空無氧氣低引力高輻射的特殊環境下生成的一種高活性生物介質，具有超越傳統產品20倍的超強大抗病毒作用，它在病毒dna復制過程當中具有超強干擾作用，可完全阻斷病毒dna復制，並可以透皮吸收深入皮下，直達皮膚基底層和真皮細胞層全面掃清病毒。
  17. Annlic the establishment gram kj medicinal preparation is one high active living thing medium which in the outside too bareness oxygen, the low attraction, under the high radiation special environment produces, has the surmounting legacy product 120 time of ultra formidable anti - virus functions, it has the ultra strong jamming function in the middle of the viral dna copy process, may completely block the viral dna duplication, and may pass the skin absorption, be thorough hypodermic, goes directly to the skin base first floor and the dermis cellular layer comprehensively sweeps clean the virus

    Annlic安立克kj劑是在外太空無氧氣低引力高輻射的特殊環境下生成的一種高活性生物介質，具有超越傳統產品20倍的超強大抗病毒作用，它在病毒dna復制過程當中具有超強干擾作用，可完全阻斷病毒dna復制，並可以透皮吸收深入皮下，直達皮膚基底層和真皮細胞層全面掃清病毒。
  18. The plant expression vector pbin19 - rok219 was constructed, which contains cauliflower mosaic virus ( camv ) 35s promoter and noster. introduction of ibdv vp2 gene under control of camv 35s promoter resulted in the construction of binary expression vector pbr - vp2. then the vp2 gene was in the left and right border regions, which denote the limits of the dna that is integrated into the plant genomic dna via agrobacterium fwme / ac / ms - mediated transformation

    構建了表達載體pbin19 - rok219 ，以ibdv甘肅天水株的抗原基因vp2為目的基因，將vp2基因置於植物組成型表達啟動子camv35s之下，構建了一個ibdvvp2基因的植物表達載體pbr - vp2 ，這樣使vp2基因位於農桿菌t - dna的左右邊界重復序列之間。
  19. Hpv is a crowd of small dna virus, at present completely has distinguished hpv has 80 many kinds of types, but and the between difference lies in the gene structure the difference

    Hpv是一群小dna病毒，目前已完全鑒別到的hpv有80多種類型，而型與型之間的差異在於基因結構的不同。
  20. Baculovirus is a kind of double - stranded circle large dna virus, which has been developed as an environment sound pesticide and a powerful vector of foreign protein expression as well as a potential vector of gene therapy

    桿狀病毒是一類雙鏈環狀dna病毒，作為生物防治殺蟲劑及高效外源蛋白表達載體得到廣泛研究。近來有許多學者致力於桿狀病毒作為基因治療載體的研究。
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