Volume 24, Number 8—August 2018
Research
Susceptibility of Human Prion Protein to Conversion by Chronic Wasting Disease Prions
Figure 1
![Western blot analysis showing detectable levels of prion protein in the chronic wasting disease–affected cervid brain specimens used to evaluate the susceptibility of the human prion protein (PrP) to conversion by chronic wasting disease prions. We analyzed brain homogenate derived from elk, white-tailed deer, and reindeer specimens by using Western blot to evaluate levels of total PrP. We subjected 2 μL of each 10% brain homogenate sample to Western blot and assessed detection of total PrP by m](/eid/images/16-1888-F1.jpg)
Figure 1. Western blot analysis showing detectable levels of prion protein in the chronic wasting disease–affected cervid brain specimens used to evaluate the susceptibility of the human prion protein (PrP) to conversion by chronic wasting disease prions. We analyzed brain homogenate derived from elk, white-tailed deer, and reindeer specimens by using Western blot to evaluate levels of total PrP. We subjected 2 μL of each 10% brain homogenate sample to Western blot and assessed detection of total PrP by mAb 6H4. We performed 3 technical repeats with similar results; a representative Western blot is shown. Reference molecular markers have been included. mAb, monoclonal antibody.
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