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Aβ plaque burden was detected using thioflavin-S [35] staining or a polyclonal Aβ antibody (diluted 1∶100, Cell signaling) and the digital image was analyzed using Image J software (NIH).
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Each BxACE was detected using BxACEPabs.
Bound receptor was detected using streptavidin-HRP.
Erythropoietin (EPO) was detected using quantifiable ELISA.
HRP activity was detected using enhanced chemiluminescence.
Immunoreactivity was detected using enhanced chemiluminescence (PerkinElmer).
The reaction was detected using ECL reagents.
Then, putative TFBS were detected using Genomatix.
Protein bands were detected using ECL (Amersham).
The proteins were detected using enhanced chemiluminescence.
Mendelian inconsistencies were detected using PedCheck (v.1.1) [35].
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