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The two arms assigned to each rat were separated by at least 2 other arms.
Peripheral blood lymphocytes from a healthy donor and spleen lymphocytes from mouse and rat were separated by density gradient centrifugation on Ficoll Hypaque (Pharmacia).
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The rats were separated into two groups.
The liver, spleen, kidney, and ovary/testis of rats were separated and weighed.
The skulls of the rats were separated and fixed with 10% formalin for micro-computed tomography (micro-CT) analysis.
Thirty-day old male WisThirty-day oldseparated into 4 groups: control, obese, calorie restriction (CR), and calorie restriction with triiodothyronine admalestration (CRT).
(H) Protein solutions from the lungs of male and female rats were separated by IEF (linear pH gradient from pH 3 to 10) and SDS-PAGE (13% polyacrylamide gel) methods, respectively.
The rats were separated into the following groups: group A, no operation without an anticancer drug (control rats); group B, a gastric operation; group C, chemotherapy; and group D, a gastric operation followed by chemotherapy.
Three ways of cranial irradiation, nasal cavity and intravascular irradiation were tested with combined injection of 125I-NT 20 μg/kg and pheophorbide 100 μg/kg to rats, and organs of rats were separated and determined the radioactivity.
108 Wistar rats were separated into euglycemic (EG) controls and STZ-treated hyperglycemic (HG) groups, and received bilateral femoral custom rectangular implants of two surface topographies: grit blasted (GB) and grit-blast with a superimposed calcium phosphate nanotopography (GB-DCD).
Hence, the present study was designed to investigate the gastrointestinal (GI) disturbances after an intraperitoneal (IP) administration of irinotecan in rats.Twenty Wistar rats were separated into two groups of ten.
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CEO of Professional Science Editing for Scientists @ prosciediting.com