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The incubators were kept in a temperature and humidity controlled animal care room, in which the temperature was set at 31°C and the relative humidity at 60%.
Mice were maintained in a temperature and humidity controlled animal facility, with a 12-hour light and dark cycle and free access to water and a standard rodent chow (D03, SAFE, Villemoisson-sur-Orge, France).
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The mice were group-housed (up to 4 mice per cage) and maintained in a temperature (22 24°C) and humidity (40 60%) controlled animal facility, with a 12 hour light:dark cycle.
The animals were housed in a temperature (22 ± 1°C) and humidity (50 ± 10%) controlled animal room on a 12 h light/dark cycle with lights on at 60 00 h.
They were housed collectively (8 rats/cage in CPP experiments) or individually (SA experiments), in a temperature (22 ± 2°C) and humidity- (55 ± 5%) controlled animal room with a 12 hr/12 hr light/dark (6 AM-6 PM) cycle.
All animals were maintained in a controlled animal facility at 20°C and 50% humidity, with a photoperiod of 12 h light/12 h dark where they were monitored daily for health as described previously [ 47].
All animals were housed in a temperature and humidity controlled room with 12-12 hours light/dark cycles, two animals per cage (Makrolon type 4, Tecniplast, VA, Italy), and were allowed normal cage activities under standard laboratory conditions.
The rats were housed at the National Institute for Occupational Safety and Health animal facility, under temperature and humidity controlled conditions and a 12-hr light/dark cycle.
Animals were kept in temperature and humidity controlled environment with a 12/12 h light and dark cycle and free access to laboratory food pallet and water.
The animals were housed in a temperature and humidity controlled environment with a 12 h light/12 h dark cycle.
Animals were maintained in a temperature and humidity controlled room, with 12 h light-dark cycles, and were allowed food and water ad libitum.
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