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Finally, the 3-Cy3 labelling reaction was performed overnight at 4C in 20 l containing 100 pmol unlabeled RNA, 0.5 mM ATP, 200 pmol pCp-Cy3 (Jena Bioscience), 10 U RiboLock RNase Inhibitor (Thermo Fisher Scientific), 1x Ligation Buffer and 10 U T4 RNA Ligase (Thermo Fisher Scientific)

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Dissection of the Endogenous Cellular Pathways of PCSK9-induced Low Density Lipoprotein Receptor Degradation: EVIDENCE FOR AN INTRACELLULAR ROUTE *

Tan Q, Akindehin SE, Orsso CE, Waldner RC, DiMarchi RD, Muller TD, et al