Bronstein I, Fortin J J, Voyta J C, Juo R R, Edwards B, Olesen C E, Lijam N, Kricka L J
Tropix, Inc., Bedford, MA.
Biotechniques. 1994 Jul;17(1):172-4, 176-7.
Chemiluminescent assays are described for the secreted alkaline phosphatase (SEAP) and beta-glucuronidase (GUS) reporter gene products. These assays provide simple, sensitive, non-isotopic alternatives to existing detection methods and are performed in microplate or tube luminometers or in a scintillation counter. The SEAP reporter gene product is secreted from mammalian cells and is thus easily detected in a sample of culture medium. Sensitive detection of secreted placental alkaline phosphatase is performed with CSPD chemiluminescent alkaline phosphatase substrate, and approximately 3 fg of enzyme can be detected. GUS has become the major reporter gene used for the analysis of plant gene expression. Sensitive chemiluminescent detection of GUS activity can be performed with an assay system we have developed using Glucuron, a beta-glucuronidase substrate. This chemiluminescent assay detects 60 fg of GUS and is linear over six orders of magnitude of enzyme concentration. CSPD and Glucuron substrates have been incorporated into two new chemiluminescent reporter gene assay kits for SEAP and GUS.
本文描述了针对分泌型碱性磷酸酶(SEAP)和β-葡萄糖醛酸酶(GUS)报告基因产物的化学发光测定法。这些测定法为现有检测方法提供了简单、灵敏、非同位素的替代方法,可在微孔板或试管发光计中或闪烁计数器中进行。SEAP报告基因产物从哺乳动物细胞中分泌出来,因此很容易在培养基样品中检测到。使用CSPD化学发光碱性磷酸酶底物可对分泌型胎盘碱性磷酸酶进行灵敏检测,大约可检测到3 fg的酶。GUS已成为用于分析植物基因表达的主要报告基因。使用我们开发的一种检测系统,利用β-葡萄糖醛酸酶底物Glucuron可对GUS活性进行灵敏的化学发光检测。这种化学发光测定法可检测到60 fg的GUS,并且在六个数量级的酶浓度范围内呈线性。CSPD和Glucuron底物已被纳入两种用于SEAP和GUS的新型化学发光报告基因检测试剂盒中。