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2 protocols using αrabbit hrp

1

Comprehensive Antibody Toolkit for Synaptic Proteins

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Primary antibodies: αSynCAM-Biotin (chicken, CM004-6, MBL), αSynCAM (rabbit, PA3-16744, Thermo Scientific), αMPP2 (rabbit, ab97290, Abcam), αPSD-95 (rabbit, ab76115, Abcam), αPSD95 (mouse, 75-028, NeuroMab), αGluA2 (mouse, 75-002, NeuroMab), αStargazin/TARPγ2 (mouse, 73-242, NeuroMab) αStargazin (rabbit, 2503S, Cell Signaling), αTubulin (rat, ab6160, Abcam), αFlag-HRP (mouse, A8592, Sigma), αHA (mouse, MMS-101R, Covance), αHA (rabbit, H6928, Sigma), αMyc (mouse, 631206, Clontech), αMYC (rabbit, 2272S, Cell Signalling), αHSV (rabbit, ab3414, Abcam), αGFP (goat, ab6663, Abcam), normal mouse IgG (sc-2025, Santa Cruz), normal rabbit IgG (sc-2027, Santa Cruz), normal chicken IgY (sc-2718, Santa Cruz). Secondary antibodies: αMouse-HRP (115-035-003, Dianova), αRabbit-HRP (111-035-003, Dianova), αRat-HRP (sc-2032, Santa Cruz), αGoat-HRP (sc-2020, Santa Cruz).
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2

Western Blot Analysis of GABA Receptor Subunits

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Lysates and beads were boiled in 2x SDS-sample buffer (8% SDS, 40% glycerol, 0.25 M Tris pH 6.8, 20% β-mercaptoethanol) for 5 minutes, separated on a 10% SDS-PAGE, and blotted onto PVDF membranes (Roche). Membranes were blocked with 5% skim milk/PBST. Primary antibodies were diluted in the blocking buffer and applied over night at 4°C, followed by 3 washes with PBST and 1 hour incubation with appropriate secondary antibodies. HRP signals were detected using Western Lightning chemiluminescent substrates (Perkin Elmer, USA) with a luminescent image analyser (ImageQuant LAS4000, GE Healthcare).
Primary antibodies: αGABAAR α1 (mouse, 75–136, NeuroMab), αFlag (mouse, F1804, Sigma), αFlag-HRP (mouse, A8592, Sigma), αGFP (chicken, ab13970, Abcam), αGST (mouse, 75–148, NeuroMab), and αHA (rabbit, H6928, Sigma).
Secondary antibodies: αMouse-HRP (115-035-003, Dianova), αMouse-native-IgG (Veriblot, 131368, Abcam), αRabbit-HRP (111-035-003, Dianova), and αChicken-HRP (ab6753, Abcam).
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