Skip to main content
. Author manuscript; available in PMC: 2008 Aug 24.
Published in final edited form as: Brain Res. 2007 Jul 26;1165:15–20. doi: 10.1016/j.brainres.2007.06.051

Fig. 1.

Fig. 1

Immunoprecipitation, dot blotting and immunostaining using various amounts of the tissue protein (1500 μg, 1000 μg, 500 μg and 100 μg) and antibody for the (a) α1-, (b) α4-, (c) α6-, (d) β2-, (e) β3-, (f) γ2-, or (g) δ-subunit of GABAA receptors. For negative control (NC), affinity-purified non-immune rabbit polyclonal IgG was used. Lane 1: 1500 μg; lane 2: 1000 μg; lane 3: 500 μg and lane 4: 100 μg of the immunoprecipitated protein from the rat cerebellum (α1-, α6-, β2-, β3-, and γ2-subunits) or hippocampus (α4-subunit). Each experiment was performed three times.