rG4 mut_AHPC_PEG2

rG4 mut_AHPC_PEG2 (30 nM; 30 min) does not bind to RHAU53 peptide, confirming that G4 structure integrity is required for interaction with DHX36 fragments^[1].
rG4 mut_AHPC_PEG2 (3 pmol; 4 h) does not colocalize with endogenous DHX36 in HeLa cells, confirming it cannot target DHX36 in cells^[1].
rG4 mut_AHPC_PEG2 (250 nM; 24 h) does not degrade DHX36 protein in HeLa cells^[1].
rG4 mut_AHPC_PEG2 (0-200 nM; 48 h) does not inhibit translation of the APP rG4 WT reporter construct in HeLa cells^[1].
rG4 mut_AHPC_PEG2 (0-100 nM; 24 h) does not reduce native APP protein expression or degrade DHX36 in HEK 293T cells^[1].
rG4 mut_AHPC_PEG2 (200 nM; 24 h) does not degrade DHX36 or reduce Gnai2 protein expression in C2C12 myoblast cells^[1].
rG4 mut_AHPC_PEG2 (200 nM; 24 h) does not impair the proliferative capacity of C2C12 myoblast cells or skeletal muscle stem cells^[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.