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[求助]
NADH还原型辅酶I在什么Buffer中保存稳定?
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我是学化学的,对生物不是很了解,最近在查阅NADH还原型辅酶I的保存Buffer的资料,看到以前的帖子有说用tris buffer PH~8的,帖子里也贴有文献, 但是只是没有文献出处,想请教各位生物高手,能否告知这篇文献的出处,或者发给我这篇文献? 另外只说了可用tris buffer PH~8,那么buffer浓度是多少呢?配制酶的浓度又是多少呢,还是酶的浓度是根据要测定的东西来定,比如我们要测定ALT,AST的, 那么NADH的浓度应该是多少呢?希望各位多多指点,万分感谢! 文献内容如下: Colowick, Kaplan, and Ciotti (4) observed that the rate of hydrolysis of the nicotinamide-ribose linkage of NAD at 100” increases with increasing pH above pH 6.0. The rates of hy- drolysis obtained in various buffers at pH 7.5 were found to de- pend on the type of buffer used. Tris and acetate buffers did not increase the rate of hydrolysis above that observed with un- buffered NAD at this pH, whereas phosphate and citrate buffers enhanced it 3- to 4-fold. It was noted (1) that Tris could almost completely abolish this stimulatory effect of phosphate and citrate buffers |
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