Roy A C, Saha N, Tan S M, Kamarul F Z, Ratnam S S
Department of Obstetrics and Gynaecology, National University of Singapore.
Electrophoresis. 1992 Jun;13(6):396-7. doi: 10.1002/elps.1150130181.
A sensitive staining method for the detection of oxytocinase (EC 3.4.11.3) activity in electrophoresis gels has been described. The method is based on the enzymatic release of p-nitroaniline (PNA) from two specific synthetic oxytocinase substrates, S-benzyl-L-cysteine-p-nitroanilide (BCN) and L-leucine-p-nitroanilide (LN), respectively. The PNA is then diazotized with sodium nitrite and subsequently coupled to a chromogen, N-(1-naphthyl)-ethylenediamine dihydrochloride (NED) to produce a deep pink/magenta colored azo-dye at the site of oxytocinase activity.
本文描述了一种用于检测电泳凝胶中催产素酶(EC 3.4.11.3)活性的灵敏染色方法。该方法基于分别从两种特定的合成催产素酶底物S-苄基-L-半胱氨酸对硝基苯胺(BCN)和L-亮氨酸对硝基苯胺(LN)中酶促释放对硝基苯胺(PNA)。然后,PNA用亚硝酸钠重氮化,随后与显色剂N-(1-萘基)-乙二胺二盐酸盐(NED)偶联,在催产素酶活性位点产生深粉色/品红色的偶氮染料。