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. 2001 Nov 13;98(24):13501–13506. doi: 10.1073/pnas.241517598

Table 4.

Postimplantation development of oocytes fertilized by ICSI with fresh, frozen, or freeze-dried spermatozoa

Sperm treatment Medium for sperm dispersion and storage Mouse strain Sperm storage time, days No. 2-cell embryos* transferred (No. exps.) No. recipients Examination on day 14 post coitum
No. (%) implants No. (%) normal fetuses Range
Fresh Hepes-CZB B6D2F1 94 (8) 12 75 (80) 54 (57)b 0–83
C57BL/6J 48 (6) 6 36 (75) 26 (54)c 29–73
129/SvJ 54 (4) 4 37 (69) 22 (41) 13–58
BALB/c 65 (4) 4 36 (55) 16 (25) 14–40
Frozen and kept at −75°C EGTA B6D2F1 Up to 28 66 (4) 8 46 (70) 31 (47) 14–70
C57BL/6J Up to 28 76 (7) 8 68 (89)a 42 (54)d 30–90
129/SvJ Up to 42 43 (4) 4 31 (72) 19 (44) 38–67
Freeze-dried and kept at 4°C EGTA B6D2F1 Up to 14 98 (5) 8 72 (73) 37 (38)b 11–56
C57BL/6J Up to 56 176 (17) 18 112 (64)a 43 (24)c,d 0–69
129/SvJ Up to 56 60 (6) 6 46 (77) 24 (40) 27–50
BALB/c Up to 35 75 (6) 6 58 (77) 16 (21) 6–40

Statistically significant χ2 comparisons between treatments within strains:  

a

,  

c

, and  

d

, P < 0.001;  

b

, P < 0.01. 

*

In all strains two-cell embryos were derived from syngeneic gametes. 

CD-1 females (albino) mated with vasectomized CD-1 males (albino). Two-cell embryos transferred on the first day of pseudopregnancy. 

Composition of EGTA medium: 50 mM NaCl, 50 mM EGTA, and 10 mM Tris⋅HCl.