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inhibitor相关的网络例句

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与 inhibitor 相关的网络例句 [注:此内容来源于网络,仅供参考]

The broth dilution method was used to determine MICs of fluoroquinolones against the QnrS-positive isolates. The accumulation of ciprofloxacin and the effect of efflux pump inhibitor, carbonyl cyanide m-chlorophenyl hydrazone for tested isolates of E.coli were measured by a fluorescenece method.

采用肉汤微量稀释法测定QnrS阳性株对氟喹诺酮类药物的MIC,荧光测定法检测盐酸环丙沙星在QnrS阳性株体内浓度的变化及能量抑制剂碳酰氰间氯苯腙对菌体内药物蓄积的影响。

The inhibitor efficiency will decrease with the increase in the concentration of hydrochloric acid.

大蒜汁在三种油田注水中也有一定的缓蚀作用,缓蚀效率在42%到64%之间。

Inhibitor of leukotriene A4 hydrolase and of enkephalin degradation in cell preparations from brain.

白三烯A4水解酶和脑细胞降解产生的脑啡肽的抑制剂。

The experiment was carried out by hydroponics and with application of ion channel inhibitor TEA at low K+ concentration.

钾是植物细胞中最丰富的离子,是植物必需大量元素之一,在植物的生长和发育中起重要作用[1-4]。

When measuring the water permeability, people used to make the cell in the circumstance of hypotonicity. Our research has contrast the other method to make the cell in the circumstance of hyperosmotic using FluoStar Optima in CHO-V163S-AQP4、FRT-V163S-AQP1 and SMMC-7221-V163S. We has confirmed that the latter is more sensitive and accurate than the former in the process of high throughput screening AQP inhibitor drug on the first time.

在测定细胞水通透性变化时,人们通常采用给细胞造成低渗环境的方法,本研究将给细胞造成高渗环境的方法与之做了对比研究,应用FluoStar Optima荧光仪对CHO-V163S-AQP4、FRT-V163S-AQP1以及SMMC-7221-V163S进行两种方法对比测定,首次证明了,在高通量药物筛选AQP阻断剂过程中,后者较前者灵敏度更高、测定结果更准确。

The research was conducted to observe the effect of hypoxanthine and a uricase inhibitor on the rat's serum uric acid levels in order to establish a new, experimental pathological model of the rat's gout.

目的:观察次黄嘌呤、尿酸酶抑制剂对大鼠血清尿酸水平的影响,拟建立一种新型实验性大鼠痛风病理模型。

MethodsThe same dosage of hypoxanthine, different uricase inhibitor are used singly or combined to replicate hyperuricemia model, inspect the uric acid in serum at different periods of time.

方法采用相同剂量次黄嘌呤,不同剂量尿酸酶抑制剂单次和连续给予复制代谢性高尿酸血症模型,测定造模后不同时段大鼠血尿酸值。

AIM To determine the optimal doses of hypoxanthine and uricase inhibitor oxonic acid potassium salt for establishment of hyperuricemia rat model, and provide experimental evidence to prepare continual hyperuricemia and gout animal model.

目的 确定次黄嘌呤与尿酸酶抑制剂氧嗪酸钾伍用制备高尿酸血症大鼠模型的合适剂量,为制备持续性高尿酸血症及痛风大鼠模型提供实验依据。

Hypoxanthine and a uricase inhibitor were combined into the model drug to work out the rat's animal model for hyperuricemia. A comparison was made between the effect of hypoxanthine and that of the model drug on the subject's serum uric acid levels. Also, such factors as the dose effect and time effect of the model-building drug were investigated.

采取合用次黄嘌呤和尿酸酶抑制剂为模型药物,制备一种尿酸生成增多型大鼠高尿酸血症动物模型,比较了单用次黄嘌呤及合用尿酸酶抑制剂对受试动物血清尿酸水平的影响,并对造模药物的量效、时效关系等因素进行了考察。

Results Hypoxanthine was administered via stomach, while unease inhibitor was injected subcutaneously by lanolin mixed with olefin, which made the uric acid in serum higher than control group about 12 hours.

结果 采用灌胃给予次黄嘌呤,皮下注射以羊毛脂石蜡油为溶剂配制的尿酸酶抑制剂,可使受试动物血尿酸值明显高于空白对照组(P.01),且可维持12h。

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