Gene doping, which is prohibited in horseracing and equestrian sports, can be performed
by introducing exogenous genes, known as transgenes, into the bodies of postnatal animals.
To detect exogenous genes, a method utilizing quantitative polymerase chain reaction
(qPCR) with a hydrolysis probe was developed to test whole blood and plasma samples,
thereby protecting the fairness of competition and the rights of stakeholders in
horseracing and equestrian sports. Therefore, we aimed to develop sample storage methods
suitable for A and B samples in gene doping tests using blood. For sample A, sufficient
qPCR detection was demonstrated after refrigeration for 1 to 2 weeks post collection. For
sample B, the following procedures were confirmed to be suitable for storage: 1)
centrifugation after sample receipt, 2) frozen storage, 3) natural thawing at room
temperature, and 4) centrifugation without mixing blood cell components. Our results
indicated that long-term cryopreservation yielded good plasma components from frozen blood
samples even though it destroyed blood cells, indicating its applicability to the gene
doping test using sample B, which can be stored for later use. Sample storage procedures
are as important as detection methods in doping tests. Therefore, the series of procedures
that we evaluated in this study will contribute to the efficient performance of gene
doping tests through qPCR using blood samples.