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Mab 1914p

Manufactured by Vector Laboratories

The MAB-1914P is a mouse monoclonal antibody produced by Vector Laboratories. It is designed for use in immunohistochemical and other immunoassay applications.

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2 protocols using mab 1914p

1

Dorsal Root Ganglion and Spinal Cord Analysis

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Dorsal root ganglia (DRG) and spinal cords were harvested from injured mAtf3pro/RmGFP reporter mice perfused with ice-cold PBS followed by cold 4% paraformaldehyde (PFA). In addition, sciatic nerves were harvested distal to the crush in treated mAtf3pro/RmGFP reporter mice perfused with cold 4% PFA. Perfused tissues were post-fixed for 3 hr at 4°C, and cryoprotected with 30% sucrose in PBS overnight. DRG sections (10 μm), spinal cord sections (20 μm) and sciatic nerve sections (60 μm) collected, blocked and permeabilized with 1% Triton X-100 in blocking buffer (Roche Diagnostics) for 1 hr at RT. Sections were incubated with rabbit polyclonal antibody against ATF3 (Santa Cruz Biotech; sc-188; 1:1000), TRPV1 (Alomone; ACC-030; 1:1000), SCG10 (Novus; NBP1-49461; 1:2000), 53BP1 (Novus; NB100-304; 1:2000), chicken polyclonal antibody against NF200 (Millipore, AB5539; 1:2000), rat polyclonal antibody against Laminin-γ (Millipore; MAB-1914P; 1:1000), DyLignt_594 conjugated Isolectin B4 (VectorLab; DL-1207; 1: 200), or mouse monoclonal antibody against phospho-Histone H2A.X (Ser139)(γ-H2AX; gamma-H2AX) (Millipore; 05-636; 1:400) at 4°C overnight and then incubated with Alexa Fluor 568 goat antibody against rabbit IgG, chicken IgG or rat IgG for 1 hr at RT. Images were acquired using a Nikon Eclipse 80I Microscope.
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2

Dorsal Root Ganglion and Spinal Cord Analysis

Check if the same lab product or an alternative is used in the 5 most similar protocols
Dorsal root ganglia (DRG) and spinal cords were harvested from injured mAtf3pro/RmGFP reporter mice perfused with ice-cold PBS followed by cold 4% paraformaldehyde (PFA). In addition, sciatic nerves were harvested distal to the crush in treated mAtf3pro/RmGFP reporter mice perfused with cold 4% PFA. Perfused tissues were post-fixed for 3 hr at 4°C, and cryoprotected with 30% sucrose in PBS overnight. DRG sections (10 μm), spinal cord sections (20 μm) and sciatic nerve sections (60 μm) collected, blocked and permeabilized with 1% Triton X-100 in blocking buffer (Roche Diagnostics) for 1 hr at RT. Sections were incubated with rabbit polyclonal antibody against ATF3 (Santa Cruz Biotech; sc-188; 1:1000), TRPV1 (Alomone; ACC-030; 1:1000), SCG10 (Novus; NBP1-49461; 1:2000), 53BP1 (Novus; NB100-304; 1:2000), chicken polyclonal antibody against NF200 (Millipore, AB5539; 1:2000), rat polyclonal antibody against Laminin-γ (Millipore; MAB-1914P; 1:1000), DyLignt_594 conjugated Isolectin B4 (VectorLab; DL-1207; 1: 200), or mouse monoclonal antibody against phospho-Histone H2A.X (Ser139)(γ-H2AX; gamma-H2AX) (Millipore; 05-636; 1:400) at 4°C overnight and then incubated with Alexa Fluor 568 goat antibody against rabbit IgG, chicken IgG or rat IgG for 1 hr at RT. Images were acquired using a Nikon Eclipse 80I Microscope.
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