Search for publications in the Transfection Database with Polyplus transfection reagents or for transfection conditions.

Over 6000 publications, 1000 cell lines and primary cells available.

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Found 5890 results :
Cell Linein vitro
in vivo		Delivered MoleculeReagentResults & Citations
HCT 116in vitroDNAjetPRIME
Zemanova, L. et al. (2015)

J Nat Prod 78, 2666-74
Flavones Inhibit the Activity of AKR1B10, a Promising Therapeutic Target for Cancer Treatment
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HeLain vitromRNAjetPEI
Bire, S. et al. (2013)

BMC Biotechnol ,
Exogenous mRNA delivery and bioavailability in gene transfer mediated by piggyBac transposition.
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HeLain vitromRNAjetPEI
Rejman, J. et al. (2010)

J Control Release 147, 385-91
mRNA transfection of cervical carcinoma and mesenchymal stem cells mediated by cationic carriers
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Human foreskin fibroblasts, IMR-90in vitromRNAjetPEI
Rohani, L. et al. (2016)

Stem Cell Res 16, 662-72
Generation of human induced pluripotent stem cells using non-synthetic mRNA
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CHO-3E7in vitroDNAPEIpro
Konitzer, J. D. et al. (2015)

PLoS One 10, e0145633
Reformatting Rituximab into Human IgG2 and IgG4 Isotypes Dramatically Improves Apoptosis Induction In Vitro
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HEK-293Tin vitroDNAPEIpro
Liesche, C. et al. (2016)

BMC Biotechnol 16, 17
Death receptor-based enrichment of Cas9-expressing cells
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HEK-293T/17in vitroDNAPEIpro
Piras, B. A. et al. (2016)

Mol Ther Methods Clin Dev 3, 16015
Distribution of AAV8 particles in cell lysates and culture media changes with time and is dependent on the recombinant vector
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HEK-293T/17in vitroDNAPEIpro
Powers, A. D. et al. (2016)

Hum Gene Ther Methods 27, 112-21
Development and Optimization of AAV hFIX Particles by Transient Transfection in an iCELLis(®) Fixed-Bed Bioreactor
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HEK-293CymR-rcTAin vitroDNAPEIpro
Venereo-Sanchez, A. et al. (2016)

Vaccine 34(29):3371-80,
Hemagglutinin and neuraminidase containing virus-like particles produced in HEK-293 suspension culture: An effective influenza vaccine candidate
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HEK-293in vitroDNAjetPRIME
Moore, R. et al. (2015)

Nucleic Acids Res 43, 1297-303
CRISPR-based self-cleaving mechanism for controllable gene delivery in human cells
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