Author: João Pedro Fonseca; Alain R. Bonny; G. Renuka Kumar; Andrew H. Ng; Jason Town; Qiu Chang Wu; Elham Aslankoohi; Susan Y. Chen; Patrick Harrigan; Lindsey C. Osimiri; Amy L. Kistler; Hana El-Samad
Title: A Toolkit for Rapid Modular Construction of Biological Circuits in Mammalian Cells Document date: 2018_12_26
ID: 1kugu5zk_30
Snippet: In the first library, we combined one of three localization tags (NLS (nucleus), NES (cytoplasm) and Lyn (plasma membrane)) with four fluorescent proteins (tagBFP, mAzamiGreen, mScarlet and iRFP713) (Fig. 5a) . Performed in parallel, this reaction generated The final library was delivered to the hAAVS1-LP HEK293T cell line described before (Fig. 4 ) to ensure single-copy integration in every cell. We visualized the expression and localization of .....
Document: In the first library, we combined one of three localization tags (NLS (nucleus), NES (cytoplasm) and Lyn (plasma membrane)) with four fluorescent proteins (tagBFP, mAzamiGreen, mScarlet and iRFP713) (Fig. 5a) . Performed in parallel, this reaction generated The final library was delivered to the hAAVS1-LP HEK293T cell line described before (Fig. 4 ) to ensure single-copy integration in every cell. We visualized the expression and localization of the fluorescent proteins after selection with Blasticidin and observed the successful random delivery of no more than 3 fluorescently-tagged subcellular compartments (Fig. 5b) , as predicted from the cloning strategy.
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