Baranov V S, Lebedev V M, Poleev A V, Mikhaĭlova E P, Rybalko A V, Shved N V
Biull Eksp Biol Med. 1990 Aug;110(8):196-8.
Samples of chorionic villi and embryonic tissues (brain, brain--sheaths) are thoroughly washed with Hank's solution, immediately subjected to hypotonic treatment (0.9% sodium citrate plus few drops of 0.01% colchicine) 37 degrees C, 30 min, prefixed 20 min with equal amount of standard fixative mixture, twice fixed in standard fixative solution (1 hour, -10 degrees C), hydrated with equal volume of distilled water (5-10 min), dried, macerated directly on the slide with 60% acetic acid. The cell suspension is then evenly spread on the slide surface, dried, postfixed and stained. The method provides sufficient amount of metaphase and prometaphase mitotic plates suitable for differentiating staining in 1.5-2 hours after sampling and might be recommended for routine chromosomal analysis in prenatal diagnosis of inherited diseases during early pregnancy.
绒毛膜绒毛和胚胎组织(脑、脑鞘)样本用汉克氏溶液彻底冲洗,立即在37℃下进行低渗处理(0.9%柠檬酸钠加几滴0.01%秋水仙碱)30分钟,用等量标准固定剂混合物预固定20分钟,在标准固定液中固定两次(1小时,-10℃),用等体积蒸馏水水化(5 - 10分钟),干燥,直接在载玻片上用60%乙酸浸解。然后将细胞悬液均匀铺展在载玻片表面,干燥,后固定并染色。该方法能提供足够数量的中期和早中期有丝分裂板,适合在取样后1.5 - 2小时进行鉴别染色,可推荐用于妊娠早期遗传性疾病产前诊断的常规染色体分析。