Khalid G, Neumann H, Flemans R J, Hayhoe F G
J Clin Pathol. 1979 May;32(5):482-7. doi: 10.1136/jcp.32.5.482.
G-banding of chromosome metaphase preparations derived from haemic cells of healthy individuals and from patients with acute myeloid leukaemia was performed with the aid of trypsin, papain, and pretreatment of the chromosome spreads with emulphogene before proteolytic digestion. Papain digestion revealed more distinguishable bands than did trypsin digestion. Pretreatment of the chromosome spreads with emulphogene greatly enhanced the number of distinguishable bands for both enzymes. The combination of pretreatment with emulphogene and digestion with papain revealed optimal numbers of bands for individual chromosomes essentially identical with those agreed at the Paris Conference 1971. The use of the emulphogene-papain technique appears also to offer an advantage in the banding of chromosomes from leukaemic cells.
利用胰蛋白酶、木瓜蛋白酶,并在蛋白水解消化前用乳化剂对染色体涂片进行预处理,对健康个体和急性髓性白血病患者血细胞来源的染色体中期标本进行G显带。木瓜蛋白酶消化显示出比胰蛋白酶消化更多的可区分带。用乳化剂对染色体涂片进行预处理极大地增加了两种酶可区分带的数量。乳化剂预处理和木瓜蛋白酶消化相结合,显示出各条染色体的最佳带数,与1971年巴黎会议商定的基本一致。乳化剂 - 木瓜蛋白酶技术在白血病细胞染色体显带方面似乎也具有优势。