Tantravahi R, Miller D A, Miller O J
Cytogenet Cell Genet. 1977;18(6):364-9. doi: 10.1159/000130782.
Metaphase chromosome preparations were made from leukocyte cultures of normal individuals. The cells were fixed in methanol:acetic acid (3:1 v/v), then dropped on cold, wet slides which were air-dried before storage at 4 degrees C. The slides were stained to identify the chromosomes by one of the following procedures: (1) Quinacrine. Slides were stained for 10 min in quinacrine mustard solution, rinsed in running tap water for 2 min, and mounted in Tris-maleat buffer, pH 5.6.
中期染色体标本取自正常个体的白细胞培养物。细胞用甲醇:乙酸(3:1 v/v)固定,然后滴在冰冷、湿润的载玻片上,空气干燥后于4℃保存。载玻片通过以下方法之一进行染色以识别染色体:(1)喹吖因。载玻片在喹吖因芥子溶液中染色10分钟,在流动自来水中冲洗2分钟,然后用pH 5.6的Tris-马来酸盐缓冲液封片。