通过放射免疫测定中的竞争性抑制来确定抗体的互补位图。
The paratope mapping of antibodies was determined by competitive inhibition in radioimmunoassay.
它们也竞争性抑制引起疾病的“坏”细菌。
They can also out-compete "bad" bacteria that may cause disease.
一个非竞争性抑制剂的净结果相当于转化某些酶成为钝化形式。
The net result of a non-competitive inhibitor is equivalent to converting some of the enzyme present to an inactive form.
酶底物动力学分析表明，马桑内酯对该酶的抑制属非竞争性抑制。
The enzyme-substrate kinetic analysis indicated that it was the noncompetitive inhibition.
用l-酪氨酸作底物，测定了牛磺酸对酪氨酸酶的非竞争性抑制。
The noncompetitive inhibition of taurine on tyrosinase was determined with L - Tyrosine as substrate.
齐多夫定会竞争性抑制司他夫定的磷酸酰化，因此禁止与齐多夫定联合用药。
Zidovudine may competitively inhibit the intracellular phosphorylation of stavudine. Therefore, use of zidovudine in combination with Stavudine is not recommended.
用L—酪氨酸作底物，测定了银杏叶提取物对酪氨酸酶的非竞争性抑制作用。
The noncompetitive inhibition of EGb on tyrosinase was determined with L-Tryosine substrate.
产物竞争性抑制的存在将增加载体颗粒内的底物浓度，对效率因子的影响较小。
The effects of competitive product inhibition are shown to increase the substrate concentration in the carrier, and, additionally, to increase the effectiveness factors slightly.
而且CYP2D6能被多种药物竞争性抑制和诱导，药物联用时易产生相互作用。
Meanwhile, many drugs can influence the activity of CYP2D6 by competitive inhibition or induction, which is easy to cause interaction in coadministration.
美伐他汀是3羟甲基戊二酰辅酶a还原酶的有效的竞争性抑制剂，它是一种胆固醇生物合成调解酶。
Mevastatin is a potent competitive inhibitor of 3-hydroxy-3-methyl-glutaryl-coa reductase, a regulatory enzyme for cholesterol biosynthesis.
美伐他汀是3羟甲基戊二酰辅酶a还原酶的有效的竞争性抑制剂，它是一种胆固醇生物合成调解酶。
Mevastatin is a potent competitive inhibitor of 3-hydroxy-3-methyl-glutaryl (HMG) -coa reductase, a regulatory enzyme for cholesterol biosynthesis.
建立了固定化纤维素酶的反应动力学模型，该模型以米氏方程为基础并考虑了产物竞争性抑制的影响。
A kinetics model was developed for predicting and simulating immobilized cellulase performance, which follows Michaelis_Menten kinetics with competitive product inhibition.
作为天然核苷受体的竞争性抑制剂，糖环部分化学改造的核苷类似物在过去的几十年中得到了深入的研究。
As competitive inhibitors of natural nucleoside receptors, sugar-modified nucleoside analogues have been well studied in the past few decades.
AG 1112对重组人ck2的动力学研究表明：它与GTP和酪蛋白分别呈混合性和非竞争性抑制作用。
Kinetic studies of AG1112 on recombinant human CK2 showed that the inhibition was mixed (competitive is dominant) with GTP and noncompetitive with casein.
槲皮素竞争性抑制CYP3A2右美沙芬N脱甲基反应，非竞争性抑制CYP2E1氯唑沙宗6羟化反应。
QU exhibited competitive inhibition of CYP3A2 dextromethorphan N-demethylation reaction and expressed noncompetitive inhibition of CYP2E1 chlorzoxazone-6-hydroxylation reaction.
竞争性抑制竞争性抑制剂与底物竞争酶的活性部位，降低酶的约束力基板的可能性，并观察到的反应速度放缓。
Competitive INHIBITION Competitive inhibitors compete with substrate for an enzyme's active site, lowering the enzyme's likelihood of binding substrate and slowing the observed reaction velocity.
AG114对重组人ck2的动力学研究表明：它与GTP呈混合竞争性抑制作用，与酪蛋白呈非竞争性抑制作用。
Kinetic studies of AG114 inhibition on recombinant human CK2 showed that the inhibition was mixed competitive with GTP and noncompetitive with casein.
在前三种底物条件下，当高底物浓度时，L-苯丙氨酸表现出反竞争性抑制作用；低底物浓度时，则呈现激活作用。
As the former three substrates were employed, at high substrate concentration, L-Phe inhibited the enzyme uncompetitively and activated the enzyme at low substrate concentration.
竞争性抑制实验显示雷帕霉素与FK506和该蛋白质的结合存在竞争性，且雷帕霉素与该蛋白质的结合能力比FK506强。
In the competitive inhibition experiment, it showed that rapamycin and FK506 could bind this protein competitively and rapamycin had better binding capacity than FK506.
竞争性抑制实验显示雷帕霉素与FK506和该蛋白质的结合存在竞争性，且雷帕霉素与该蛋白质的结合能力比FK506强。
In the competitive inhibition experiment, it showed that rapamycin and FK506 could bind this protein competitively and rapamycin had better binding capacity than FK506.
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