proenzyme

MMP-3 proenzyme protein expression could be detected in normal rat liver .

在正常大鼠肝组织中有MMP-3的酶原表达。

Results Preparations of highly purified MBL and proenzyme MASPs were obtained .

结果获得高度纯化的MBL和酶原形式的MASP。

AIM To investigate the dynamic alteration of gelatinase A ( metalloproteinase-2 , mmp-2 ) proenzyme protein expression in the process of experimental liver fibrosis .

目的研究实验性肝纤维化过程中明胶酶A（mmp-2）酶原蛋白表达的动态变化。

Caspase-3 proenzyme is composed of one large-subunit and one small-subunit and only after being cut and activated can Caspase-3 perform its function .

该酶原由一个大亚基和一个小亚基组成，只有被切开并激活后Caspase-3才能够行使其功能。

The carbon tetrachloride-induced hepatic fibrosis rat models were used . MMP-3 proenzyme protein expression in the different stages of liver fibrosis was measured by half quantitative analysis of Western blot .

建立四氯化碳中毒性大鼠肝纤维化模型，采用半定量Western免疫印迹方法，对肝纤维化不同阶段肝内MMP-3的酶原蛋白的表达水平进行了检测。

Of the system , P0 is one of the important components ; it has two activities , MPO and DPO , and exists as proenzyme PPO in the insect .

其中，PO是PPO系统的关键成分之一，它是以酶原形式PPO存在于昆虫体内，具有MPO和DPO两种酶活性。

MAIN OUTCOME MEASURE : cellular mitochondrial function , cellular caspase 9 and caspase 3 activity , release of mitochondrial CytC and cleavage of caspase 3 proenzyme .

主要观察指标：细胞线粒体功能、细胞内caspase-9和caspase-3活性、线粒体细胞色素C的释放和caspase-3酶原的降解。

Splittings of synovial cell of rheumatoid arthritis and asparagic acid specific cysteine protease-3 proenzyme treated with resveratrol in various concentrations for 24 hours were studied with Western-blot method .

采用Western-blot分析不同浓度白藜芦醇处理24h的类风湿关节炎滑膜细胞，天冬氨酸特异性半胱氨酸蛋白酶3酶原的裂解。