, Coronal slices (50-80 ?m thickness) of striatum and SNc were processed for Tyrosine hydroxylase(TH)-immunohistochemistry, after endogenous peroxidases inactivation, using a rabbit anti-TH (1/1000, 36 h at 4°C, AB152, Merck Millipore), and biotinylated goat antibody against rabbit IgG (1/200, BA 1000, Vector Laboratories, CliniSciences
, /YFP) or 72 h (SST/YFP) at 4°C; and secondary antibodies: donkey anti-rabbit coupled to Alexa647 (1/500, 711-605-152, Efficacy and specificity of transgenic mouse lines. Coronal slices (30-50 ?m) from Pv::ChR2 or Sst::ChR2 mice were processed for immunostaining of PV or SST, and YFP, pp.712-605
, Floating coronal sections (60 ?m) were incubated (2 h at RT) in Alexa 488-conjugated streptavidin (1/250, S11223, Invitrogen, Thermofisher) in References
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