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1.PEROXIDATION EFFECTS ON LIPOSOME OF ACTIVE OXYGEN SPECIES PRODUCED BY THE SYSTEM OF ADP-FeCl_3-XANTHINE-XANTHINE OXIDASE
ADP-FeCl_3-黄嘌呤-黄嘌呤氧化酶体系产生的活性氧对脂质体的过氧化影响收藏指正
2.METHODS :①Studies on xanthine oxidase(XO) inhibitory activity of Qi salt in vitro ;
方法 :通过体外测定黄嘌呤氧化酶 (XO)抑制率来观察Qi盐对UA形成的影响 ;收藏指正
3.A study on the resistance of transfected cells with hSOD gene to superoxide a_nion_induced cytotoxicity caused by paraquat and xanthine (X)/xanthine oxidase (XO) is carried out in this paper.
研究了已获得稳定表达的hSOD基因导入细胞 (CMV -SOD细胞 )对百草枯 (paraquat)和黄嘌呤 (X) /黄嘌呤氧化酶 (XO)产生的超氧阴离子造成的细胞毒性的抵抗作用 .收藏指正
4.METHODS: Aortic smooth muscle cells from 4-6months-healthy abortive fetuses were incubated for 24 hours with xanthine (100 μmol/L) and xanthine oxidase (5 U/L) in vitro .
方法 :体外培养胎儿主动脉平滑肌细胞 ,加入含 10 0 μmol/L黄嘌呤 ,5U/L黄嘌呤氧化酶的无血清培养液 ,孵育 2 4h ,收集细胞上清液。收藏指正
5.Determination of hypoxanthine and xanthine in fish by the coupled reaction of enzyme (fluorometric method)
酶偶联反应测定鱼中的次黄嘌呤和黄嘌呤(萤光光度法)收藏指正
6.Objective To explore the effect of propofol on xanthine oxidase(XO) activity during hepatic ischemia-reperfusion injury (HIRI).
目的　探讨异丙酚对肝缺血 /再灌注损伤 (HIRI)时黄嘌呤氧化酶 (XO)活性的影响。收藏指正
7.ESR spectrum of hypoxanthine-xanthine oxidase and Fe ++ —H 2O 2 system were significantly reduced or disappear by NADH.
NADH使得次黄嘌呤—黄嘌呤氧化酶体系和Fe+ + —H2 O2 体系的ESR信号明显减弱甚至消失 ;收藏指正
8.A novel technology to determine the activity of xanthine oxidase(XOD) through the chromogenic reaction of 4-aminoantipyrine(AAP),phenic acid(PA) and hydrogen peroxide(H_2O_2),which was produced via the oxidation of xanthine catalyzed by XOD,under the help of horseradish peroxidase(HRP) was(proposed).
研究了以辣根过氧化物酶-苯酚-4-氨基安替比林反应显色新体系,检测黄嘌呤氧化酶(XOD)活力的新方法。收藏指正
9.This paper describes a new method for determination of xanthine (Xa) at a poly (acridine orange)(POAO)modified electrode by 2.5th order differential voltammetry.
报道了聚吖啶橙 (POAO)修饰电极多阶半微分伏安法测定黄嘌呤 (Xa)。收藏指正
10.Method Cultured CAEC were incubated with xanthine(26.3 μmol·L 1 )plus xanthine oxidase (17u·L 1 )(X XO)for 4 hours. The contents of NO,ET 1,PGE 2 and TXA 2 were measured by means of Griess assay,immunoradiation assay and ELISA,respectively.
方法培养的犬呼吸道上皮细胞与黄嘌呤（26．3μmol·L?1）及黄嘌呤氧化酶（17u·L?1）孵育4h后，应用酶联免疫、放射免疫及Gries还原法，测定条件培养液中NO，ET?1，PGE2和TXA2含量。收藏指正
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