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Likewise, oxidizing conditions promote disulfide formation (GSSG and Pr-S-S-G), which may reduce bioavailability of GSH and counteract some of the potential benefits of GSH administration

HA-OxyR, Tpx1, Tpx1.SO 2 H, Pap1, and Trx1 were immuno-detected with monoclonal house-made anti-HA antibodies, or with anti-Tpx1 [23], anti-peroxiredoxin-SO3 antibody (LabFrontier, Seoul, South Korea), anti-Pap1 [13], and anti-Trx1 [39] polyclonal antibodies, respectively