Use of a composition which regulates oxidation/reduction reactions intracellularly and/or extracellularly in a staining or sorting process
A composition and cell technology, applied in the field of sorting and staining sperm cells, can solve the problems of reduced forward motility and the like
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Embodiment 1
[0091] Bull semen was collected from sexually mature bulls using an artificial vagina, and the samples were diluted with 2 parts of carbonate buffer and transferred to the staining facility in a temperature-controlled container at 25°C. Once received, the semen was analyzed for concentration, motility, and motility using the Hamilton-Thorn Motility Analyzer (IVOS) according to standard and well-known methods (Farrell et al., Theriogenology, 49(4):871-9 (March 1998)). sex and forward motility. Depending on the semen concentration, pipette a small aliquot of the carbonated sperm suspension, centrifuge it at 500Xg for 5 minutes, remove the supernatant and resuspend the pellet in TCA buffer, pH 7.3 at 41°C, to prepare 1 mL of 150×10 6 Sperm / ml of suspension. An additional 1 mL of 150 × 10 6 Sperm / ml suspension. Aliquots of 10 mM Hoechst in water were added to the sperm suspension to give a dye concentration of 400 μM Hoechst. The sperm suspension was left in a 41°C water bath ...
Embodiment 2
[0093] Sperm samples were obtained and prepared in the same manner as in Example 1 except for the following differences: the buffers used to suspend sperm for staining and IVOS analysis were TCA and TCA containing 10 μM vitamin K. The results of the IVOS analysis are summarized in figure 2 .
Embodiment 3
[0095] Sperm samples were obtained and prepared in the same manner as in Example 1 except for the following differences: the buffers used to suspend sperm for staining and IVOS analysis were TCA and TCA containing 100 μM vitamin K. The results of the IVOS analysis are summarized in image 3 .
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