Camiolo S M, Siuta M R, Madeja J M
Prep Biochem. 1982;12(4):297-305. doi: 10.1080/00327488208065678.
Quantitation of plasminogen activators present in tissue may depend to a large extent on the extraction procedure used to solubilize the enzymes. Potassium thiocyanate solution is known to be an efficient solubilizer, but it can inhibit assay systems other than fibrin plates. An equally effective acetate-detergent extractant is reported here which can be used with the highly sensitive azocaseinolytic assay procedure. The results indicate that a three-fold increase in activator activity can be extracted from selected tissues relative to that previously reported for a phosphate-detergent extractant. The extraction medium contains 75 mM K acetate, 0.3 M NaCl, 0.1 M L-arginine, 10 mM EDTA, 0.25% Triton X-100, final pH 4.2.
组织中纤溶酶原激活剂的定量在很大程度上可能取决于用于溶解这些酶的提取程序。硫氰酸钾溶液是一种有效的增溶剂,但它会抑制除纤维蛋白平板以外的检测系统。本文报道了一种同样有效的醋酸盐 - 去污剂提取剂,它可用于高度灵敏的偶氮酪蛋白分解检测程序。结果表明,相对于先前报道的磷酸盐 - 去污剂提取剂,从选定组织中提取的激活剂活性可提高三倍。提取介质包含75 mM醋酸钾、0.3 M氯化钠、0.1 M L - 精氨酸、10 mM乙二胺四乙酸、0.25% Triton X - 100,最终pH值为4.2。