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HAF016). A specific band was detected for RAMP1 at approximately 17 kDa (as indicated). This experiment was conducted under reducing conditions and using Immunoblot Buffer Group 1." class="big_lightbox" target="_blank">
CTS013). Tissue was stained using the Anti-Sheep HRP-DAB Cell & Tissue Staining Kit (brown; Catalog # CTS019) and counterstained with hematoxylin (blue). Specific staining was localized to neuronal and glial processes. View our protocol for Chromogenic IHC Staining of Paraffin-embedded Tissue Sections." class="big_lightbox" target="_blank">
VC006). Before incubation with the primary antibody, tissue was subjected to heat-induced epitope retrieval using Antigen Retrieval Reagent-Basic (CTS013). Tissue was stained using DAB (brown) and counterstained with hematoxylin (blue). Specific staining was localized to vasculature. Staining was performed using our protocol forIHC Staining with VisUCyte HRP Polymer Detection Reagents." class="big_lightbox" target="_blank">
![Western Blot RAMP1 Antibody [Unconjugated]](http://images.novusbio.com/images/antibody/RAMP1_AF6428_Western_Blot_9866.jpg)
![Immunohistochemistry RAMP1 Antibody [Unconjugated]](http://images.novusbio.com/images/antibody/RAMP1_AF6428_Immunohistochemistry_11302.jpg)
![Immunohistochemistry RAMP1 Antibody [Unconjugated]](http://images.novusbio.com/images/antibody/af6428_human-ramp1-affinity-purified-polyclonal-ab-immunohistochemistry-27102020154839.jpg)
