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Sperm preservation is a valuable technique for maintaining genetic resources in biomedical research. In the present study, 10mM Tris–HCl and 1mM EDTA (TE buffer; a simple solution without cryoprotection), was used to freeze or freeze-dry rat sperm. The results were compared with rat sperm frozen using a solution containing Equex STM and egg yolk. Sperm from Wistar and Sprague–Dawley (SD) rats were...
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