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Cy2 conjugated goat anti mouse

Manufactured by Jackson ImmunoResearch

Cy2-conjugated goat anti-mouse is a secondary antibody conjugated with the Cy2 fluorescent dye. It is designed to detect and label mouse primary antibodies in various immunoassays and imaging applications.

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3 protocols using cy2 conjugated goat anti mouse

1

Immunohistochemistry of Synuclein and Neurotransmitters

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The following primary antibodies were used: mouse anti-α-Syn (BD610787, BD Biosciences, Franklin Lakes, NJ), rabbit anti-V5 (ab9116, Abcam, Cambridge, UK), mouse anti-α-Syn (LB509, Covance, Munich, Germany), rabbit anti-TH (Zytomed, Berlin, Germany), rabbit anti-TPH2 (ABN60, Millipore, Darmstadt, Germany), mouse anti-NeuN (MAB377, Millipore) and mouse anti-β-tubulin (Sigma, St- Louis, MO).
The following secondary antibodies were used: Cy2-conjugated goat anti-mouse, Cy3-conjugated goat anti-rabbit, Cy3-conjugated goat anti-mouse, Cy5-conjugated goat anti-rabbit (all from Jackson Immuno Research, West Grove, PA); horseradish peroxidase(HRP)-coupled goat anti-mouse and HRP-coupled goat anti-rabbit (both from Dianova, Hamburg, Germany).
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2

Collagen I Coated Coverslip Immunostaining

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Glass coverslips were coated with 10 μg/ml collagen I (BD Biosciences) at 4 °C overnight, then rinsed three times with PBS. Cells were plated on coverslips in normal culture medium and allowed to adhere for 4 hours before fixation. Cells were fixed, permeabilized, and immunostained as described previously57 (link). Briefly, cells were fixed for 15 minutes with 4% paraformaldehyde containing 10 mM PIPES, pH 6.8, 2 mM EGTA, 2 mM MgCl2, 7% sucrose and 100 mM KCl for 15 min at room temperature, and permeabilized with 0.25% Triton X-100. Cells were blocked for 1 hour with 3% BSA + 1% goat serum in PBS. The following primary antibodies were used at indicated concentrations and incubated at 4 °C overnight: rat anti-CD104 (439-9B, BD Pharmingen, 1:100) mouse anti-Laminin-5 (γ2 chain, clone D4B5, Millipore, 1:500 dilution) in 3% BSA in PBST overnight at 4 °C. Cy3-conjugated goat anti-rat and Cy2-conjugated goat anti-mouse (Jackson Immuno Research, 1:500) and Alexa Fluor 647 phalloidin were incubated with 3% + 1% goat serum BSA for 1 hour at room temperature in dark. Coverslips were mounted on glass slides using 50% glycerol solution and sealed with clear polish. Images were acquired by total internal reflection (TIRF) microscopy using a Nikon Eclipse Ti. Images were processed for colocalization analysis and Pearson’s correlation coefficient by NIS Elements AR 3.2 software.
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3

Dual Immunofluorescence for KLF11 and Active Caspase-3

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To determine KLF11 co-expression with active Caspase-3, additional sections were incubated with mouse anti-KLF11 monoclonal (1:250; Cat# SC136101, Lot# 60209; Santa Cruz Biotechnology, Dallas, TX) and rabbit anti-active caspase-3 polyclonal (1:250; Cat# 9661, Lot# 38; Cell Signaling Technology, Danvers, MA) antibodies. Visualization was made by secondary incubation with Cy2 conjugated goat anti-mouse (1:1000; Jackson) and Cy3 conjugated goat anti-rabbit (1:1000; Jackson). Lastly, all sections were rinsed with PBS and mounted with Vectashield mounting medium containing DAPI (Vector Labortories).
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