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ML相关的网络例句
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Can scavenge DPPH·strongly with IC_(50) of 0.164 mg/mL, and inhibit hemolysis of mice erythrocyte evidently with IC_(50) of 0.112 mg/mL. The reactive oxygen species resistant power of mice serum is enhanced by the pigment, the concentration of MDA resulting from peroxidation of lipid in mice liver tissue can be reduced, and the swelling of mice liver mitochondria can also be restrained. The preventing experiments of the pigment of Lycium ruthenicum Murr.

在药理学研究中体外抗氧化实验表明,PLR具有一定的抗氧化能力,表现出很强的DPPH·自由基清除活性,IC_(50)达到0.164 mg/mL;能显著的抑制小鼠红细胞溶血,IC_(50)为0.112mg/mL;能增强小鼠血清抗活性氧能力,抑制小鼠肝组织脂质过氧化产物MDA生成和小鼠肝线粒体肿胀度,并显示出一定的量效关系。

A549 cell line was stimulated with LPS (10 μg/mL) and then treated with Rs504393 (10 μg/mL) for 6 hours. ALI model was established with intranasal administration of LPS (5 mg/kg) in C57BL/6J mice. RS504393 (5 mg/kg) was administered 30 min before LPS dripped nasally. IL-8, IL-1β, plasminogen activator inhibitor-1, monocyte chemoattractant protein-2, and the expressions of CCR1 and CCR2b were studied by using Realtime-RT-PCR, ELISA and cyto-flowmetry.

体外实验选用A549细胞系,应用LPS(10μg/mL)刺激合并RS504393(10μg/mL)治疗6 h后,流式细胞仪技术检测CCR1和CCR2的表达,ELISA法检测细胞培养上清液内白介素-8的浓度;体内实验选用C57BL/6J小鼠,腹腔注射RS504393(5 mg/kg)预处理30 min后经鼻滴入JPS(5 mg/kg),LPS刺激4 h后收集BALF和肺脏标本,计数BALF内细胞总数,应用BCA法检测BALF内蛋白浓度,Realtime-RT PCR和ELISA法检测BALF和肺脏IL-1β、凝血酶原激活物抑制物-1和单核细胞趋化蛋白-2的表达。

Within the range of 1 X 10-8~9.72 10-10 g/ml, the concentration of Np and intensity to the fluorescence of Tiron-Tb present relations of linearity, the detection limit for Np is 0.127ng/ml, nearly 1000 times high of uranium does not interfere the determination of the neptunium.

在1×10~(-8)~9.72×10~(-10)g/ml范围内,Np的浓度与Tiron-Tb的相对荧光强度呈线性关系,方法检出限:1.27×10~(-10)g/ml,将近1000倍的铀存在时不产生干扰。

The results indicated that the amount of IL-6 from HDPCs stimulated by 100μg/ml LPS significantly decreased by 2.5、5、10、20μg/ml Chinese nutgall water extract in a dose-depent manner.

结果显示2.5、5、10、20μg/ml五倍子水提取物能明显抑制25μg/ml的LPS诱导HDPCs分泌IL-6,并呈浓度依赖性。

The results indicated that 100μg/ml LPS had significant damage on the ultrastructure of HDPCs . After 5μg/ml Chinese nutgall water extract were added , the damage of HDPCs'ultrastructure was decreased significantly.

结果显示100μg/ml内毒素对牙髓细胞超微结构有不同程度的损伤,加入5μg/ml五倍子水提取物后,牙髓细胞超微结构损伤明显减轻,细胞器结构基本恢复正常。

The additional supplements including glucose,ascorbic acid and insulin had the enhancement effects on C.andersoni development,while folic acid had no significantly effect on C. andersoni development and calcium pantothenate had inhibited effect.When added 50 mmol/L glucose,50μg/ml ascorbic acid,0.3 U/ml insulin into 10%FCS RPMI-1640 medium,the proliferation of C.andersoni had a great significantly increase,and the gene copies of C.andersoni were 8-fold compared with that in 10%FCS RPMI-1640 medium.

冻融法+蛋白酶K法+声裂法提纯隐孢子虫卵囊DNA效果最佳,其次为冻融法+声裂法和蛋白酶K法+声裂法,冻融法+蛋白酶K法效果最差。10%FCS是培养安氏隐孢子虫的最佳FCS浓度,葡萄糖、维生素C和胰岛素都具有促安氏隐孢子虫增殖作用,泛酸钙无促虫体增殖效果,而叶酸则抑制虫体增殖。10%FCS RPMI-1640培养液中加入50 mmol/L葡萄糖,50μg/ml维生素C和0.3 U/ml胰岛素促安氏隐孢子虫增殖效果最显著,虫体增殖8倍。

No interference was found with conventional drugs, except vancomycin and methylprednisolone. The average concentrations of phenacetin and paracetarnol were (5.94 ± 4.79) and (8.81 ± 2.91)μg/mL in serum,(3.25 ± 1.10) and (570.45 ± 187.13)μg/mL in urine in the 13 healthy volunteers.

除万古霉素和甲泼尼龙外,其他临床常用药物对测定无干扰。13名健康受试者血清中非那西丁和总对乙酰氨基酚浓度为(5.94±4.79)和(8.81±2.91)μg/mL;尿液中非那西丁和总对乙酰氨基酚浓度为(3.25±1.10)和(570.45±187.13)μg/mL。

However,the extracts of the plants with petroleum ether,at the concentration of 5mg/mL,resulted in a mortality of(34.77%) or 19.22% with or without light treatment,respectively,showing the effects of photoactivation.

猪毛蒿精油浓度0.5 mg/mL和5 mg/mL时,不显示出光活化效应,但在1 mg/mL时则表现出显著的光活化效果,光照与非光照的死亡率分别为83.65%和24.15%。

Using a VOLUMETRIC PIPET, pipet 1.0 mL of the acid mixture into a 30-50 mL

用 管移取1.0 mL酸混合物到一个30-50 mL的烧杯中。

When ready to start the kinetics trials, pipet 3 mL of one of the K3[Fe6]-NaNO3 solutions into an Erlenmeyer flask, and add 3 mL of the ascorbic acid-HNO3-EDTA solution.

准备开始做动力学试验时,用移液管移取其中一种K3[Fe6]-NaNO3溶液 3 mL,加到锥形瓶中,然后加入3 mL抗坏血酸-HNO3-EDTA溶液溶液F

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呼气,收缩臀部肌肉;拱起身体,尽量抬起头来,右腿伸直朝向天花板(膝微屈,以避免肌肉紧张)。

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