Fig 7. Protective function of WRAB18 on LDH activity under severe conditions.

LDH solution was cultured with BSA, sucrose solution, and PBS buffer, and purified WRAB18 was dehydrated to 70%, rehydrated to the original volume, supplemented with 200 mM NaCl for 2 h, placed on ice for 12 h, and left at 45°C for 30 min. Reactions were repeated three times. Statistically significant differences were analyzed using Student’s t-test (*p<0.05 or **p<0.01).