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A rather simple but very effective method of removing dominant epitopes to enhance responses to conserved subdominant epitopes involved the removal of the S1 portion of spike containing the RBD and then the administration of a vaccine with only S2 as a DNA vaccine or protein [73] (Table 2)

The assay plate was sealed and incubated at room temperature with gentle shaking for 30 min (300 rpm) while protected from light

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Anti-Doping Agency, many of these are not approved for human use, are often sold from unregulated sources, and can lead to positive drug tests