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. Author manuscript; available in PMC: 2009 Dec 15.
Published in final edited form as: J Neuroimmunol. 2008 Oct 31;205(1-2):94–100. doi: 10.1016/j.jneuroim.2008.09.013

Figure 3.

Figure 3

Western blot analysis of non-PK treated brain homogenates following capture ELISA assay. The capture ELISA assay was carried out on normal sheep (NS), scrapie-infected sheep (SS), normal deer (ND), CWD-infected deer (CWD), normal hamster (NH) and 263K-infected hamsters (263K) under the same conditions as described for Figure 2 using a non-biotinylated detection reagent. The material was eluted from the microtiter plate as described in Materials and Methods and Western blotted. Immunostaining was carried out using Mab 8E9.