Brown T D, Rickwood D, MacGillivray A J, Klein G
J Gen Virol. 1978 Sep;40(3):511-7. doi: 10.1099/0022-1317-40-3-511.
EBNA-containing chromatin from Raji cells was solubilized by treatment with high concentrations of urea and salt and fractionated by hydroxyapatite chromatography. Fractions eluting at different phosphate concentrations were analysed for the presence of EBNA by means of an anti-EBNA-specific 125I-labelled IgG absorption assay. The antigen was found in fractions containing non-histone chromatin proteins.
来自拉吉细胞的含EBNA染色质通过用高浓度尿素和盐处理使其溶解,并通过羟基磷灰石色谱法进行分级分离。通过抗EBNA特异性的125I标记IgG吸收测定法分析在不同磷酸盐浓度下洗脱的级分中是否存在EBNA。该抗原存在于含有非组蛋白染色质蛋白的级分中。