Fig 1: Flow cytometry of HEK-293 cells transfected with RHO-AC-mGFP. Top row: Flow cytometry allows one to investigate the relationship between total levels of rhodopsin (green fluorescent protein [GFP] intensity) and levels of rhodopsin at the cell surface (APC-Cy7). Here are shown wild-type transfections (A) and transfections of the G106R variant (B). A control sample treated with the secondary detection antibody alone (C) is shown for comparison of APC-Cy7 intensities. Two discrete populations can be seen in each culture, with transfected cells at high GFP levels (boxed region) versus non-transfected cells. Bottom row: Histograms showing the relative intensity of rhodopsin expression at the cell surface (D–E) compared to controls treated with the secondary detection antibody alone (F).
Fig 2: Map of the RHO-AC-mGFP plasmid. The restriction enzymes Sgf I and Mlu I were used to extract the rhodopsin ORF from plasmid RC211328 and insert it into the vector pCMV6-AC-mGFP (Map constructed using SnapGene®, GSL Biotech; snapgene.com).
Supplier Page from OriGene Technologies for Rhodopsin (RHO) (NM_000539) Human Untagged Clone