这是一篇有关pcDNA mammalian expression vector的综述，是根据61篇发表使用实验的文章归纳的。这综述旨在帮助来邦网的访客找到最适合pcDNA mammalian expression vector。
默克密理博中国
为了研究泛素连接酶对离子稳态的调节作用，使用了Novagen公司的pcDNA5-FRT/TO-3xHA-3xFLAG载体来进行亚克隆。至该文献
赛默飞世尔显示:30; 总数:60
为了研究信号肽连接药物对融合蛋白转位的抑制作用，采用了Invitrogen公司的pcDNA3表达载体，进行DNA克隆实验。至该文献
为了研究TLR和模式识别受体Siglec家族蛋白相互作用及调控，采用了Life technologies公司的pCDNA6载体，进行DNA克隆实验。至该文献
为了研究CDON在调节肿瘤细胞存活中的作用，Invitrogen的pcDNA3.1 Directional TOPO表达试剂盒被用于进行DNA克隆。至该文献
为了研究白藜芦醇对肌肉中线粒体合成的影响，Invitrogen的pCDNA3.1质粒被用于进行蛋白表达。至该文献
为了研究PTC124药理学活性的作用机制，Invitrogen的pcDNA3质粒被用于进行DNA克隆。至该文献
为了研究PI3K gamma的激活机制，Invitrogen的pcDNA3质粒被用于进行蛋白表达。至该文献
为了研究脱酰胺过程对Bcl-xL降解的调控作用，Invitrogen的pcDNA/TR载体被用于进行DNA克隆。至该文献
为了研究UNC93B1介导的内涵体Toll样受体不同的运输机制，采用Invitrogen公司的pCDNA3.1真核表达载体进行DNA克隆试验。至该文献
为了研究Stat5信号在基础及应激红细胞生成过程中的动态特性，采用了Invitrogen的pcDNA3载体进行DNA克隆实验。至该文献
为了癌细胞生长受PFK1糖基化调控，采用了Invitrogen的pcDNA3.1/Hygro进行蛋白表达实验。至该文献
为了研究蛋白可以CUG为起始密码子进行翻译以为MHC class I提供所需肽段，采用了Invitrogen的pcDNA1 vector进行质粒构建实验。至该文献
为了研究线粒体功能异常癌症细胞的有氧酵解过程中NOX的作用，采用了Invitrogen公司的vector pcDNA4/TO，进行DNA克隆实验。至该文献
为了研究Fam20C参与了胞外蛋白的磷酸化,Invitrogen的pcDNA4.0质粒被用于进行蛋白表达。至该文献
为了研究AMPK能够被水杨酸直接激活，采用了Life Technologies的pcDNA5FRTTO进行质粒构建实验。至该文献
为了研究朗格汉斯细胞介导的PAH代谢能导致DNA损伤和肿瘤发生，采用Invitrogen的pcDNA6.2 TM/GW/D-TOPO expression vector进行质粒构建实验。至该文献
为了研究LARGE蛋白具有木糖基转移酶和葡糖醛转移酶活性以修饰肌营养不良蛋白聚糖让其发挥正常功能，采用了Invitrogen的pcDNA3 vector进行蛋白表达实验。至该文献
为了研究韧皮运输需要SWEET蛋白介导的糖外流，采用Invitrogen的pcDNA3.1(-)进行质粒构建实验。至该文献
为了研究XMRV质粒DNA可能污染了慢性疲劳综合症病人的外周血单核细胞DNA，采用Invitrogen的pcDNA3.1(-)进行DNA测序实验。至该文献
为了研究受体调控的离子通道被改造出来用于人为操纵神经电活动，采用Invitrogen的pcDNA3.1进行基因表达实验。至该文献
为了研究5mC和5hmC能够被Tet加双氧酶转换成5caC并进一步被TDG清除，采用Invitrogen的pcDNA4进行蛋白表达实验。至该文献
为了研究小鼠血糖能够通过人工合成的光遗传学转录元件进行调控，采用Invitrogen的pcDNA3.1进行载体构建实验。至该文献
为了研究PSF在生物钟负反馈调节中有重要作用，采用Invitrogen的pcDNA3进行luciferase 实验。至该文献
为了揭示UVR8蛋白通过一种基于色氨酸的机制感应紫外线B辐射，采用Invitrogen的pcDNA-DEST40载体进行细胞转染。至该文献
为了研究秀丽隐杆线虫（C. elegans）融合蛋白家族成员AFF-1蛋白的结构和功能，采用Invitrogen的pCDNA3.1(+)载体构建质粒。至该文献
为了研究RACK1和蛋白激酶C alpha在哺乳动物生物钟中所起的作用，使用了英杰公司的pcDNA3.1-Flag来进行亚克隆。至该文献
为了研究牛痘病毒实现细胞间快速传播的机制，使用了英杰公司的pcDNA3来进行亚克隆。至该文献
为了研究牛痘病毒实现细胞间快速传播的机制，使用了英杰公司的pcDNA3来进行亚克隆。至该文献
为了研究miR-206在神经损伤后的神经突触再生过程中所起的作用，使用了英杰公司的pcDNA 6.2-GW/EmGFP-miR载体来进行亚克隆。至该文献
为了研究纺锤体装配检验点蛋白在减数第一次分裂过程中所起的作用，使用了英杰公司的pcDNA-3载体来进行亚克隆。至该文献
为了研究AMPK对生物钟调控的机制，使用了英杰公司的pcDNA3.1/v5-His-TOPO载体来进行亚克隆。至该文献
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