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2 protocols using mouse anti tau 12 6400

1

Drosophila Larval Neurobiology Staining

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Third-instar larvae were dissected in ice-cold PBS and fixed in 4% paraformaldehyde for 30 min. The fixed tissues were stained following standard procedures. The primary antibodies used were: mouse anti-DLG, anti-Futsch and anti-β-tubulin antibodies from the Developmental Studies Hybridoma Bank; rabbit anti-DVGlut (Daniels et al., 2004 (link)), rabbit anti-GFP (A11122, Invitrogen) at 1:1000, rabbit anti-mCherry (632496, Clontech) at 1:1000, mouse anti-acetylated tubulin (T6793, Sigma) 1:1000, mouse anti-Tau (12-6400, Invitrogen) at 1:1000, Cy3-conjugated goat anti-HRP, and Cy5-conjugated goat anti-HRP. The following secondary antibodies (from Jackson ImmunoResearch) were used: Cy3-conjugated goat anti-rabbit IgG at 1:1000, Dylight-488-conjugated anti-mouse IgG at 1:1000, and Alexa-Fluor-647-conjugated goat anti-HRP at 1:1000.
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2

Larval Nervous System Immunostaining

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Third instar larvae were dissected in ice-cold PBS and fixed in 4% PFA for 30 min. The fixed tissues were stained following standard procedures. The primary antibodies used were: mouse anti-DLG, anti-Futsch and anti-β-Tubulin antibodies from Developmental Studies Hybridoma Bank; rabbit anti-DVGlut (54) , rabbit anti-GFP (A11122, Invitrogen) at 1:1000, rabbit anti-mCherry (632496, Clontech) at 1:1000, mouse anti-Acetylated Tubulin (T6793, Sigma) 1:1,000, mouse anti-Tau (12-6400, Invitrogen) at 1: 1000, Cy3-conjugated goat anti-HRP, and Cy5conjugated goat anti-HRP. The following secondary antibodies (from Jackson ImmunoResearch ) were used: Cy3-conjugated goat anti-rabbit IgG at 1:1000, Dylight-488conjugated anti-mouse IgG at 1:1000, and Alexa-Fluor-647-conjugated goat anti-HRP at 1:1000.
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