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   家蚕细胞 的翻译结果: 查询用时:0.994秒
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蚕蜂与野生动物保护
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家蚕细胞     
相关语句
  bombyx mori cells
     Comparison of four promoters for transient expression of RFP reporter gene in cultured Bombyx mori cells (Bm-e-HNU5)
     四种启动子调控RFP报告基因在家蚕细胞(Bm-e-HNU5)内的瞬时表达
短句来源
     CHANGES OF MICROFILAMENTS IN AC-NPV-INFECTED BOMBYX MORI CELLS
     Ac-NPV感染家蚕细胞后微丝系统的变化
短句来源
     The Boinbyx mori nuclear polyhedrosis virus (BmNPV) and Bombyx mori cells as well as silkworm larvae were used successfully for mass production of biological active recombinant proteins.
     家蚕核多角体病毒(Bombyx mori Nuclear Polyhedrosis Virus.BmNPV)和家蚕细胞已成功地用来大量生产具有生物活性的重组蛋白。
短句来源
     Expression of Human Angiostatin(K1-3) Gene in Bombyx Mori Cells and Larvae of Sikworms and Its Activity Assays in Vitro & in Vivo
     人血管抑制素(K1-3)在家蚕细胞和幼虫中的表达及其生物活性研究
短句来源
     Expression of gp67 Signal Peptide-hEGF Fused Gene in Bombyx Mori Cells and Larvae of Silkworm and Its Activity Assays
     gp67信号肽—人表皮生长因子融合基因在家蚕细胞和幼虫中表达及生物活性的研究
短句来源
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  silkworm cells
     Expression of HBeAg Gene with Baculovirus Vector in Silk Worm Cells
     用杆状病毒载体在家蚕细胞中表达HBeAg基因
短句来源
     EXPRESSION OF SCHISTOSOMA JAPONICUN FATTY ACID BINDING PROTEIN GENE IN SILKWORM CELLS AND LARVAE *
     日本血吸虫脂肪酸结合蛋白基因在家蚕细胞及幼虫中的表达
短句来源
     Expression of HBeAg Gene with Baculovirus Vector in Silk Worm Cells and its Expression Product Purification
     用杆状病毒载体在家蚕细胞中表达HBeAg基因及其表达产物纯化的研究
短句来源
     To investigate the effect of dsRNA on silkworm cells, we transfected three kinds of synthetic dsRNAs of 435bp(Api), 300bp(Ap2) and 399bp(AM) in length against the various regions of BmNPV's DNA polymerase gene and DNA helicase gene, which are indispensable for viral replication in silkworm cells by TransMessenger? transfection Reagent.
     本实验中我们在国际上首次应用BmNPV来研究RNAi,以BmNPV复制必需的DNA解旋酶基因和DNA聚合酶基因为靶序列,人工设计并合成了长度分别为435bp(Ap_1),300bp(Ap_2)和399bp(A_H)的三条dsRNAs,利用TransMessenger~(TM) transfection Reagent转染家蚕细胞,研究其对BmNPV复制的抑制效果。
短句来源
     Chimeric Antibody Production in Silkworm Cells and Silkworm Larvae
     家蚕细胞和虫体产生抗人小细胞肺癌抗体
短句来源
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  bm cells
     A plasmid pGL2Rz has been constructed, which can express a triplet ribozyme R426 in Bm cells. R426 contains three hammerhead ribozymes (R47, R208 and R687) targeled to three different sites of BmNPVIE mRNA.
     用自行设计的能专一切割家蚕核多角体病毒即刻早期蛋白(BmNPVIE)mRNA上三个位点的三联体ribozyme-R426(由R47,R208和R687三个ribozyme串联而成),构建了在家蚕细胞中瞬时表达的质粒pGL2Rz。
短句来源
     After co transfection of Bm cells with wild type BmNPV and recombinant transfer vector, recombinant viruses were selected by using combination of limit dilution dot hybridization and plaque techniques.
     以重组转移载体与野生型BmNPV共转染家蚕细胞,用有限稀释法点杂交结合空斑技术纯化重组病毒。
短句来源
     Fluorescent antibody test indicated that on the surface of the plasma membrane and plasma of Bm cells infected with recombinant virus, a strong fluorescent reaction occurred.
     用荧光抗体试验检查重组病毒感染的家蚕细胞,可见感染细胞的胞浆及胞膜出现强荧光反应
短句来源
  bombyx mori cell
     Transient Expression of β-Galactosidase in Bombyx mori Cell(Bm-N) under the Regulation of Fibroin Gene Promoter
     家蚕丝蛋白基因启动子调控β-半乳糖苷酶在家蚕细胞系中的瞬时表达
短句来源
     Expression of Human IFNα 2b-THYα 1 Fused Gene in Bombyx mori Cell and Study of Its Bioactivity
     人干扰素α2b-胸腺肽α1融合基因在家蚕细胞中的表达和活性研究
短句来源

 

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  bombyx mori cells
Heat shock response in Bombyx mori cells infected by nuclear polyhedrosis virus (NPV)
      
Silkworm (Bombyx mori) cells are characterized by the ability to synthesize heat shock proteins (hsps) at exceptionally high temperatures (up to 48° C).
      
When the Bombyx mori cells (Bm-N) were transfected with the pBmgp64Luc, different treatments were undertaken.
      
  silkworm cells
Site-specific gene integration in cultured silkworm cells mediated by φC31 integrase
      
The upstream region showed complete homology to the strong promoter of the AcMNPVp10, suggesting that this promoter from BmNPV could also be exploited for high-level expression of cloned foreign genes in silkworm cells or larvae.
      
  bm cells
Following application of gelatin microspheres containing TGF-β1, with or without BM cells to skull bone defects, bone formation at the defect was assessed by soft X-ray, dual energy X-ray absorptometry (DEXA), and histological examinations.
      
After implantation for 6 weeks, gelatin microspheres containing 0.05 μg of TGF-β1 plus 106 of BM cells induced bone formation at the 6 mm diameter bone defect.
      
The defect was histologically closed by newly formed bone tissue, whilst both gelatin microspheres containing 0.05 μg of TGF-β1, and 106 and 107 of BM cells were ineffective.
      
A DEXA experiment revealed that combination of gelatin microspheres containing TGF-β1 with BM cells enhanced the bone mineral density at the skull defect to a significantly greater extent than other agents.
      
These findings indicate that a combination of gelatin microspheres containing TGF-β1 enabled BM cells to enhance the osteoinductive ability, resulting in bone formation even at the cell number at which BM cells alone were ineffective.
      
更多          
  bombyx mori cell
Expression of spider flagelliform silk protein in Bombyx mori cell line by a novel Bac-to-Bac/BmNPV baculovirus expression syste
      
Molecular characterization of a stably transformed Bombyx mori cell line: identification of alternative transcriptional initiati
      
We have isolated a stably transformed Bombyx mori cell line containing a novel selectable marker gene, puromycin N-acetyl transferase, under control of transcriptional regulatory signals from the A3 cytoplasmic actin gene.
      
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