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EXP002409

Paper

Nanogels Enable Efficient miRNA Delivery and Target Gene Downregulation in Transfection-Resistant Multiple Myeloma Cells (2019)

Peptide

HIV-1 TAT

Sequence: CGRKKRRQRRR

RNA

miRNA

All experiment fields

Experiment Id EXP002409
Paper Nanogels Enable Efficient miRNA Delivery and Target Gene Downregulation in Transfection-Resistant Mu
Peptide HIV-1 TAT
Delivery Success Class no
In Vivo Flag no
Uptake Confirmed yes
Label Confidence high
In Vitro Functional Effect yes
Endosomal Escape Evidence
Peptide Concentration ~9.5 TAT molecules per nanogel particle
Rna Concentration 0.8–1.6 nmol miR-34a per formulation
Mixing Ratio 5:1 N/P, 1.6 nmol miR-34a
Formulation Format redox-sensitive poly(glycidol) nanogel
Formulation Components poly(glycidol) nanogel + covalently bound TAT peptide + complexed miR-34a
Size Nm 207.00
Zeta Mv 3.00
Model Scope in_vitro
Model Type in vitro
Cell Lines Or Primary Cells OPM-2 multiple myeloma cells (also screened: MM.1S, AMO-1)
Animal Model
Administration Route cell culture incubation with nanogels
Output Type target gene downregulation
Output Value Significant downregulation of Notch1, Hey1, Hes1, Hes6
Output Units
Output Notes NG TAT/miR-34a-3 shows efficient uptake (SIM + flow cytometry) and functional miR-34a-mediated gene regulation.
Toxicity Notes Low cytotoxicity; viability reduction only after functional miR-34a delivery
Curation Notes