摘要
从孵化48~55小时鸡胚中抽取血液,每只胚胎可获血液2~6μl左右。一步法离心分离原始生殖细胞,可使其浓度由0.1%以下提高到50%以上。将多余血细胞用微量吸管移走后,加入添加10%胎牛血清的TCM—199做为培养基,37.5℃,5%CO2,95%空气,饱和湿度下培养,原始生殖细胞可成活24小时左右。
Blood of 48hr- 55hr chick embryoes was drawn from heart or vitelline vein. Two-six microliters of blood could be drawn from each embryo.After one-step centrifugation, chick PGCs. could be concentrated from 0. 1 % to 50%,at the interface of b 6.3%(w/v)and 14.4 %(w/v)Ficou bilayer.Moved out the other blood cells with a micropipitte,added TCM - 199with 10% FCS to the PGCs as culture medium,in-vitro cultured in anincub ator with condition of 37. 5℃,5% CO2 and saturatinn,moisture,chick PGCs could survive for about 24hrs.
出处
《生物技术》
CAS
CSCD
1996年第2期11-13,共3页
Biotechnology
关键词
鸡
原始生殖细胞
体外培养
分离
Chick
Primordial Germ Cells
In-Vitro Culture