Cryopreservation of oocytes and embryos in assisted reproductive technology for application in domestic animals and humans is very important to preserve the maternal and paternal genetic complements. Cryopreservation allows widespread use of valuable animal embryos to improve the chances of pregnancy. However, intracellular ice formation in cryopreservation methods for oocytes and embryos can lead to fatal damage. To overcome this issue of intracellular ice formation, slow freezing and vitrification methods are most widely used (Mucci et al., 2006).The balance of redox reactions in cells is very crucial for maintaining the metabolic environment and gene expression during embryonic development. However, high levels of reactive oxygen species (ROS) were seen in preimplantation embryos of cattle (Min et al., 2014). ROS, such as hydrogen peroxide, cause oxidative stress, which is known to cause DNA damage and apoptosis (Takahashi, 2012). Therefore, regulating oxidative stress and ROS production during the vitrification-warming process is criti-