Takahashi) primary antibodies, and Alexa BMN 673 molecular weight 546 goat anti-mouse secondary antibodies (Invitrogen). All experiments were approved by the local committee on animal care and conformed to the national guidelines (CCAC; http://www.ccac.ca). Cortical neurons were dissociated from E14 C57BL/6 mice, and plated on 35 mm dishes layered with poly-D-lysine coated slides at a density of 5 × 105 cells/cm2. Starting medium consisted of high glucose DMEM supplemented with 40% FBS. Cells were maintained at 37°C and 5% CO2 for 2–6 hr, after which the media was changed to Neurobasal A (GIBCO) supplemented with B-27, glutamine, and sodium

pyruvate. Cells were transfected with 2 μg of target shRNA (pJH3044) or scrambled shRNA (pJH3045) constructs using Lipofectamine 2000 at DIV6. Recordings were performed at DIV8. Leak currents of the primary mouse cortical neurons were recorded in

whole-cell configuration at 20°C–22°C, modified from Lu et al. (2007) and Raman et al. (2000). Trametinib cost The pipette solution contained (in mM): K-Gluconate 115; KCl 25; CaCl2 0.1; MgCl2 5; BAPTA 1; HEPES 10; Na2ATP 5; Na2GTP 0.5; cAMP 0.5; cGMP 0.5, pH 7.2 with KOH, ∼320 mOsm. The bath solution consisted of (in mM): NaCl 150; KCl 5; CaCl2 2; MgCl2 4; D-glucose 10; sucrose 5; HEPES 10, TEACl 1, CsCl 2, pH 7.4 with Tris-OH, ∼320 mOsm. For 15mM Na+ solution, [Na+]o was supplemented with Tris+. Cells with steady state leak currents −40 to 5 pA at −85 mV were analyzed. To test the efficacy of mNLF-1 knockdown, 2 μg pJH3096 (mNLF-1::RFP) were cotransfected with Endonuclease 2 μg pJH3044 or pJH3045. Western blot analysis was performed with antibodies against RFP (Chromoteck) at 1:1,000. nlf-1(hp428) animals

carrying an integrated NCA-1::GFP (or NCA-2::GFP) reporter, and an extrachromosomal array expressing NLF-1 cDNA under Phsp-16.2 (pPD49.78) were maintained at 15°C. L4 stage animals were transferred to 32°C for 3h, and maintained at 25°C overnight prior to confocal imaging. Information on strains and constructs, quantitative epifluorescent and confocal microscopy, and membrane yeast two-hybrid (MYTH) assays are provided in Supplemental Information. We thank the Caenorhabditis Genetics Center and National Bioresource Project for strains, Cori Bargmann for ER and Golgi markers and UNC-2 cDNA, Mario de Bono for EGL-19::GFP strains, Mike Nonet for UNC-10 antibodies, and Dejian Ren for NALCN and mUNC-80 cDNAs. We thank Sharon Ng, Hang Li, Taizo Kawano, Zhi Xu, and Dan Zu for technical and programming support, Victoria Wong and Ria Lim for advice on MYTH and shRNA knockdown, respectively, and H. McNeill and S. Cordes for access to equipments and reagents. S.M.A. was supported by a National Sciences and Engineering Research Council postgraduate fellowship. This work was supported by the Canadian Institute of Health Research grants (MOP74530 and MOP123250) to M.Z. I.S. received Canadian Institute of Health Research grants.