Protein samples were run according to standard protein separation procedures, using SDS-PAGE. The following primary antibodies were used: mouse α-GFP (1:2000; Roche Cat# 11814460001, RRID:AB_390913), mouse α-myc (1:2000; Santa Cruz Biotechnology Cat# sc-40, RRID:AB_627268), rat α-RBP10 (1/500; RRID:AB_2890154), rabbit α-aldolase (1/2000; RRID:AB_2890155). We used horseradish peroxidase coupled secondary antibodies (1:2000; Bio-Rad Cat# 170–6516, RRID:AB_11125547; Bio-Rad Cat# 170–6515, RRID:AB_11125142). Blots were developed using an enhanced chemiluminescence kit (Amersham; RPN2209) according to the manufacturer’s instructions. Densitometry was performed using Fiji v. 2.0.0.

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