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The binding affinities of mAbs to PV1 sVLPs were measured using an Octet RED96 System (FortBio, a Sartorius company, USA)

doi: 10.1101/2020.09.01.278747 269

In vivo three-photon imaging of activity of GCaMP6-labeled neurons deep in intact mouse brain

Immunofluorescence co-localization analysis confirmed that MEF2C expression precisely overlapped with established pericyte markers NG2 and RGS5 (Supplementary Fig

This would point to a pathway in which, in contrast to the METAP1-NatA/E situation, a primary role of NAC may not simply be the recruitment of the modifying enzyme, but also that of a chaperone acting after modification together with its potential co-chaperone NMT1 to facilitate substrate folding

Guo D, Tong Y, Jiang X, Meng Y, Jiang H, Du L, et al