Endo Y
J Chromatogr. 1981 Jan 23;205(1):155-64. doi: 10.1016/s0021-9673(00)81823-3.
Histamine, putrescine, spermidine, spermine and histone H1 in tissue extracts were separated step by step on a small cellulose phosphate column (3 x 0.6 cm). Borate buffers (pH 8.5) of different ionic strength were used for the separation. Histamine was determined fluorimetrically by reaction with o-phthalaldehyde. Other substances were determined spectrophotometrically by reaction with 2,4,6-trinitrobenzene sulphonate or fluorimetrically by reaction with fluorescamine. Quantitative determinations can be carried out on 0.1 nmol of histamine, about 1 nmol of polyamines and 0.5 microgram of histone H1 by fluorimetry, and 10--20 nmol of polyamines and 50 micrograms of histone H1 by spectrophotometry. The method is simple, does not require costly equipment and allows the analysis of many samples simultaneously.
组织提取物中的组胺、腐胺、亚精胺、精胺和组蛋白H1在一根小型磷酸纤维素柱(3×0.6厘米)上逐步分离。使用不同离子强度的硼酸盐缓冲液(pH 8.5)进行分离。组胺通过与邻苯二甲醛反应采用荧光法测定。其他物质通过与2,4,6 - 三硝基苯磺酸盐反应采用分光光度法测定,或通过与荧光胺反应采用荧光法测定。通过荧光法可对0.1纳摩尔组胺、约1纳摩尔多胺和0.5微克组蛋白H1进行定量测定,通过分光光度法可对10 - 20纳摩尔多胺和50微克组蛋白H1进行定量测定。该方法简单,无需昂贵设备,且能同时分析多个样品。