22 (link) antibodies. The next day, slides were washed and incubated for 1 hour at room temperature with Alexa Fluor‐conjugated secondary antibodies (1:1000, Life Technologies). After washing, slides were incubated with DAPI (1:2000) for 5 minutes and mounted with DABCO (Sigma‐Aldrich). Images were acquired using an Axiolab fluorescence microscope (Zeiss).
Immunocytochemistry Analysis of Neural Markers
22 (link) antibodies. The next day, slides were washed and incubated for 1 hour at room temperature with Alexa Fluor‐conjugated secondary antibodies (1:1000, Life Technologies). After washing, slides were incubated with DAPI (1:2000) for 5 minutes and mounted with DABCO (Sigma‐Aldrich). Images were acquired using an Axiolab fluorescence microscope (Zeiss).
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Corresponding Organization :
Other organizations : University of Verona, University of Brescia, Azienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia, University of Zurich, University of Padua, International Centre for Genetic Engineering and Biotechnology, University of Milan, Scuola Internazionale Superiore di Studi Avanzati, Indiana University – Purdue University Indianapolis
Variable analysis
- Primary antibodies used for immunocytochemistry: anti-β3 tubulin, anti-β4 tubulin, anti-CK18, anti-p62, anti-PGP9.5, anti-TARDBP, anti-TDP-43 C-term, anti-TDP-43 pS409/410
- Immunocytochemistry results, including localization and expression of the proteins targeted by the primary antibodies
- Incubation time and temperature for primary antibodies (overnight at 4°C)
- Incubation time and temperature for secondary antibodies (1 hour at room temperature)
- DAPI staining for 5 minutes
- Mounting medium (DABCO)
- No positive or negative controls were explicitly mentioned in the provided information.
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