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

Over 4000 publications, 1000 cell lines and primary cells available.

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Found 1982 results :
Cell Linein vitro
in vivo
Delivered MoleculeReagentResults & Citations
HEK-293T, Hep-2in vitroDNA, siRNAjetPRIME
Qu, S. Y. et al. (2017)

Cancer Med 6, 1389-1398
YY1 directly suppresses MYCT1 leading to laryngeal tumorigenesis and progress
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HEK-293, MRC-5in vitroDNAjetPRIME
Rathore, A. P. et al. (2013)

Virol J 10, 36
Differential unfolded protein response during Chikungunya and Sindbis virus infection: CHIKV nsP4 suppresses eIF2alpha phosphorylation
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HEK-293in vitroDNAjetPRIME
Sermersheim M.. et al. (2020)

Nat Commun 11, 3624
MG53 suppresses interferon-
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NB-15, SH-EPin vitroDNA, siRNAjetPRIME
Salcher, S. et al. (2017)

Mol Cancer 16, 95
C10ORF10/DEPP-mediated ROS accumulation is a critical modulator of FOXO3-induced autophagy
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B16-F10, G-361, HUVEC, MCF7, MDCKin vitroDNA, siRNAjetPEI, jetPRIME
Rodriguez, M. I. et al. (2013)

PLoS Genet 9, e1003531
PARP-1 regulates metastatic melanoma through modulation of vimentin-induced malignant transformation
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H9c2in vitroDNAjetPRIME
Niemann B. et al. (2020)

Cells 9, 1229
CTRP9 Mediates Protective Effects in Cardiomyocytes via AMPK-and Adiponectin Receptor-Mediated Induction of Anti-Oxidant Response
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MCF7in vitroDNAjetPRIME
Shen, Y. et al. (2017)

PLoS Comput Biol 13, e1005599
Systematic, network-based characterization of therapeutic target inhibitors
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HeLain vitroDNAjetPRIME
Saka, H. A. et al. (2015)

PLoS ONE 10, e0124630
Chlamydia trachomatis Infection Leads to Defined Alterations to the Lipid Droplet Proteome in Epithelial Cells
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HEK-293in vitroDNAjetPRIME
Posternak G. et al. (2020)

Nat Chem Biol 16, 1170-1178
Functional characterization of a PROTAC directed against BRAF mutant V600E
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Human primary fibroblastsin vitroDNAjetPRIME
Straub, I. R. et al. (2018)

Hum Mol Genet 27, 178-189
Loss of CHCHD10-CHCHD2 complexes required for respiration underlies the pathogenicity of a CHCHD10 mutation in ALS
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