这是一篇有关Gateway供体载体的综述，是根据12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Gateway供体载体。
赛默飞世尔
为了研究荚膜组织胞浆菌温度响应性毒力变化的机制，Invitrogen的pDONR/Zeo质粒被用于进行DNA克隆。至该文献
为了研究由植物表皮内特长链脂肪酸合成通过抑制细胞增殖控制的植物器官生长，采用了Invitrogen的Gateway entry vector pDONR221构建质粒。至该文献
为了研究线虫中piRNAs的特性，采用了Invitrogen的pDONR 221进行质粒构建实验。至该文献
为了通过群体测序研究黑猩猩的精细遗传图谱，采用了Invitrogen的pDONR 221 vector进行DNA测序实验。至该文献
为了研究小鼠中器官的正常发育需要B型的核纤层蛋白的功能，采用Invitrogen的pDONR201进行质粒构建实验。至该文献
为了研究酵母可以用来模仿Abeta的毒性以筛选可能的修饰基因，采用Invitrogen的pDONR221进行质粒构建实验。至该文献
为了研究伴侣蛋白能够促进转录因子KNOTTED1在细胞之间穿梭，采用Invitrogen的pDONR207进行miRNA克隆实验。至该文献
为了研究有限的植物免疫中枢被独立演化的毒力效应蛋白攻击，采用Invitrogen的pDONR/zeo进行DNA克隆实验。至该文献
为了揭示RNA聚合酶II与Med17之间具有直接相互作用，采用Invitrogen的pDONR201 载体用于基因克隆。至该文献
为了研究拟南芥中异硫氰酸烯丙酯介导的非寄主抗性能被假单胞菌sax基因产物阻断，采用Invitrogen的pDONR进行DNA克隆实验。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pDONR221载体来进行亚克隆。至该文献
为了研究在人体中GW182与Ago2的相互作用和GW182在哺乳动物miRNA通路中的作用，采用Invitrogen公司的 pDONR207 载体，进行基因缺失载体构造。至该文献
文章列表
  1. Sinem Beyhan et al. (2013). "A temperature-responsive network links cell shape and virulence traits in a primary fungal pathogen".PMID 23935449
  2. Takashi Nobusawa et al. (2013). "Synthesis of very-long-chain fatty acids in the epidermis controls plant organ growth by restricting cell proliferation".PMID 23585732
  3. Marloes P Bagijn et al. (2012). "Function, targets, and evolution of Caenorhabditis elegans piRNAs".PMID 22700655
  4. Adam Auton et al. (2012). "A fine-scale chimpanzee genetic map from population sequencing".PMID 22422862
  5. Youngjo Kim et al. (2011). "Mouse B-type lamins are required for proper organogenesis but not by embryonic stem cells".PMID 22116031
  6. Sebastian Treusch et al. (2011). "Functional links between Aβ toxicity, endocytic trafficking, and Alzheimer's disease risk factors in yeast".PMID 22033521
  7. Xianfeng Morgan Xu et al. (2011). "Chaperonins facilitate KNOTTED1 cell-to-cell trafficking and stem cell function".PMID 21868675
  8. M Shahid Mukhtar et al. (2011). "Independently evolved virulence effectors converge onto hubs in a plant immune system network".PMID 21798943
  9. Julie Soutourina et al. (2011). "Direct interaction of RNA polymerase II and mediator required for transcription in vivo".PMID 21415355
  10. Jun Fan et al. (2011). "Pseudomonas sax genes overcome aliphatic isothiocyanate-mediated non-host resistance in Arabidopsis".PMID 21385714
  11. Katja A Lamia et al. (2009). "AMPK regulates the circadian clock by cryptochrome phosphorylation and degradation".PMID 19833968
  12. Shang L Lian et al. (2009). "The C-terminal half of human Ago2 binds to multiple GW-rich regions of GW182 and requires GW182 to mediate silencing".PMID 19324964