Abstract
A simplified, fast, and innovative method was developed to count the total cell number in blastocysts. Murine blastocysts (N = 195) were used in this study. They were obtained after 10h culture of initial blastocysts, compact morulae grades I and II recovered from superovulated mouse. After culture, the blastococysts were selected to test the new proposal of counting. The process was done after embryo fixation in a sodium citrate solution, and adherence in glass slide. Following, the coloration was done using a fast panoptic coloration kit. As a result, it was possible to identify the blastomeres and count them in each blastocyst. This method provided a fast and effective analysis of the total cell number when compared with other techniques. Moreover, this new method shows advantages related to the cell visualization, which can be done in more simple equipment like stereoscopic microscope. Other interesting observed point was the long period of time and quality that the coloration stays on slides, considering other techniques.
Highlights
À FAPEMIG, pelo apoio financeiro; à CAPES, pela concessão da bolsa de estudo; e à Germovet, por ceder equipamentos e material para a realização deste estudo
Murine blastocysts (N = 195) were used in this study. They were obtained after 10h culture of initial blastocysts, compact morulae grades I and II recovered from superovulated mouse
The blastococysts were selected to test the new proposal of counting
Summary
À FAPEMIG, pelo apoio financeiro; à CAPES, pela concessão da bolsa de estudo; e à Germovet, por ceder equipamentos e material para a realização deste estudo. A simplified, fast, and innovative method was developed to count the total cell number in blastocysts.
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