chimeric protein 中文意思是什麼

chimeric protein 解釋
嵌合蛋白
  1. We find the chimeric protein in leaf epidermal cells, stomatal guard cell and root epidermal cell. actin filaments can be visualized clearly in guard cell, in guard cells of open stomata under light, actin filaments arrange reticulate randomly in cytoplasm. in guard cells of closed stomata under darkness, actin filaments arrange curly along the longitude of guard cell

    在葉片的表皮細胞、保衛細胞、根部的皮層細胞中有融合蛋白的表達,保衛細胞中微絲標記狀況良好,經光誘導處于開放態的氣孔的保衛細胞微絲呈網狀結構,在細胞內無規則分佈;經黑暗誘導處于關閉態的氣孔保衛細胞中微絲束沿保衛細胞縱軸排列,呈捲曲狀分佈。
  2. Using confocal laser scanning microscopy ( clsm ), we observed the distribution of chimeric protein in different kinds of tissues and cells in transgenic toreniafournieri

    經激光共聚焦顯微鏡觀察了轉基因植株的各種不同組織中融合蛋白的表達和分佈情況。
  3. To get in vivo evidences that apoplast calmodulin con 1d regulate plant growth and development process, a chimeric secretion form of calmodulin binding peptide, which contains a signal peptide, a calmodulin binding domain and a c - myc epitope was constructed. the chimeric gene was introduced into arabidopsis. it was expected that the overexpression of this chimeric protein could be secreted into cell wall and bound to apoplast calmodulin, which could reduce the apoplast calmoduin concentration to make an apoplast camodulin " antisense " plant. by observing the potential phenotype change of apoplast calmodulin " antisense " plant, the in vivo function of apoplast calmodulin on plant growth and developmental process could be speculated

    但這些多是採用生理學手段和藥理學方法而得出的體外( invitro )實驗結果,為了取得質外體cam在植物生長發育過程中發揮重要作用的invivo實驗證據,根據動物中的一些研究方法,本實驗設計並構建了帶有信號肽、 cam結合肽( can小肽) 、 epitope ( c - myc )融合基因的載體,並將融合基因通過真空滲入法轉入擬南芥,預期過表達的融合蛋白將會被分泌到細胞外並與質外體cam相結合,這樣就會抑制質外體cam的功能,從而可以構建質外體cam的「反義」植株,通過觀察質外體cam 「反義植株」的表型改變,就可以推斷質外體cam在植物生長發育過程中的功能。
  4. The recombinant pcr technic was used to introduce a linking peptide klgggg to the site between scfv single chain form of the monoclonal antibody sz - 51 specific for the glycoprotein gmp140 on activated platelet membrane and uk32 low molecular weight form of pro - urokinase, to make the scfv - linker - uk32 chimeric gene. this gene was cloned into the transfer vector pbacpak9, and cotransfected with bacpak6 bsu36i digest into sf 9 cells. the fusion protein was secreted into the medium. in the fifth day after the cotransfection, the supernatant of the medium showed 107 iu ml fibrinolytic activity, higher than 25 iu ml fibrinolytic activity of scfv - uk32. elisa showed that the supernatant had the binding activity to activated platelet. wastern blotting also indicated that the supernatant could bind to the monoclonal antibody of urokinase b chain

    為了提高重組導向溶栓分子scfv - uk32的溶纖活性,通過重組pcr方法在編碼scfv與uk32的堿基之間引入編碼klgggg連接肽的堿基序列,並克隆到轉移載體pbacpak9上,通過與線性病毒dna bacpak6 bsu36i digest共轉染到昆蟲細胞sf 9內,進行表達。表達產物分泌到上清中,共轉染后第5d天用纖維平板法測得sf 9細胞上清溶纖活性達到107 iu ml ,比未引入連接肽的scfv - uk32的表達活性25 iu ml高。
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