Anti-GAP43抗体- Neuronal Marker (ab12274)

Western blot showing detection of GAP43 in Mouse Whole brain tissue lysates using ab12274 (1/5000) in conjunction with a goat anti-rabbit secondary antibody conjugated to HRP (1/10000). Ab12274 did not detect GAP43 in Sciatic nerve lysates (negative control). Western blot showing detection of GAP43 in Mouse Whole brain tissue lysates using ab12274 (1/5000) in conjunction with a goat anti-rabbit secondary antibody conjugated to HRP (1/10000). Ab12274 did not detect GAP43 in Sciatic nerve lysates (negative control).

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Ab12274 staining human neuropil. Staining is localized to the cytoplasm and membrane.
Left panel: with primary antibody diluted 1:2000. Right panel: isotype control.
Sections were stained using an automated system (Dako PT Link), at room temperature. Sections were rehydrated and antigen retrieved with the Dako 3-in-1 antigen retrieval buffer, citrate pH 6.0. Slides were peroxidase blocked in 3% H2O2 in methanol for 10 minutes. They were then blocked with Dako Protein block for 10 minutes (containing casein 0.25% in PBS) then incubated with primary antibody for 20 minutes and detected with Dako Envision Flex amplification kit for 30 minutes. Colorimetric detection was completed with diaminobenzidine for 5 minutes. Slides were counterstained with Haematoxylin and coverslipped under DePeX. Please note that for manual staining we recommend to optimize the primary antibody concentration and incubation time (overnight incubation), and amplification may be required.