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l-laudanine相关的网络例句

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与 l-laudanine 相关的网络例句 [注:此内容来源于网络,仅供参考]

L Hello! We are from China.l We want to Change to the flight LH3814 to Venise. The departing time is 16:15.l Where shall we get the boarding card?

您好!我们来自中国;l 我们要乘LH3814航班转机前往威尼斯,抵离时间是16:15.l 能否告知我们该在哪里办理登机牌?

Vmax of high and low affinitive L-arginine transport decreased about 50.5% and 45.8% respectively (P<0.01). Oral adiminstration of L-arginine improved vascular NO production, cGMP content (P<0.01) and Vmax of L-arginine transport.

口服L-Arg治疗的大鼠血管NO生成和cGMP含量都较钙超载大鼠明显增高(P< 0.01),L-Arg高、低亲和性转运的Vmax增加。

Vmax of high and low affinitive L-arginine transport decreased about 50.5% and 45.8% respectively (P<0.01). Oral adiminstration of L-arginine improved vascular NO production, cGMP content (P<0.01) and Vmax of L-arginine transport.

口服L-Arg 女性治疗的大鼠血管NO生成和cGMP含量都较钙超载大鼠丰满明显增高(P< 0.01),L-Arg高、低亲和性转运的Vmax增加。

He activity of y-GT also had dose- dependent and time-dependent effect and became lowest on day 7 at the concentration of 0.5 and 1.0 umol/L. The activity of TAT increased. On day 4, the cells treated with 0.25, 0.5 and 1.0 umol/L of As2O3 had higher activity compared with control group (P.05) and it continued afterwhile.

AT随着各给药组时间的延长而上升,并随给药剂量增大而上升程度更大,培养第4天,0.25 μmol/L浓度的亚砷酸组TAT的比活性较对照组高(P<0.05),0.5 μmol/L、1 μmol/L浓度的亚砷酸组TAT的比活性较对照组更高(P<0.01),以后各天给药组均高于对照组(P<0.01)。

Responses of stomata to different concentration of NaCl stress (0,50,150,300 and 500 mmol · L-1), stomatal movements and differentiation of different phyllotaxyleaves after long time treated with 300 mmol · L-1 NaCl were investigated using the Amaranthus tricolor L.

为材料,研究了不同浓度(0、50、150、300、500 mmol · L-1)NaCl 处理后气孔的应答反应和300 mmol · L-1 NaCl 长时间处理后对不同叶序叶片气孔开闭和分化的影响。

Poly-[N-(2-hydroxyethyl)-L-glutamine] was then obtained by aminolysis of PBLG with 2-aminoethanol.

以L -谷氨酸为单体,经r -羧基的苄基保护,与光气/甲苯液反应制备L-谷氨酸苄酯的羧酸酐,均聚得L -谷氨酸苄酯,然后经由 2 -氨基乙醇胺解得聚 [N -( 2 -羟乙基)-L -谷酰胺 ] 。

Methods: Picric performance rate method is used to measure anhemolytic samples, factitious hemolytic samples, post-factitious hemolytic samples with 0.88mol/L H2O2 37℃ water bath for 20min, post-factitious hemolytic samples with 0.88mol/L H2O2 37℃ water bath for 30min, anhemolytic samples with 0.88mol/L H2O2 37℃ water bath for 20min to deal with five of the numeral value of creatinine in blood samples.

用苦味酸速率法测定未溶血、人为溶血、人为溶血后加0.88mol/L H2O237℃水浴20m in、人为溶血后加0.88mol/LH2O2 37℃水浴30min、未溶血加0.88mol/L H2O2 37℃水浴20m in五种处理的血液样品中肌酐值。

The linear ranges all were 5~200 mg/L and the detection limits (S/N=3) were 0.20 and 0.15 mg/L for arsanilic acid and sulfanilic acid, respectively.

阿散酸和对氨基苯磺酸的线性范围均为5~200 mg/L,检出限(S/N=3)分别为0.20 mg/L和0.15 mg/L。

The apparent quantum efficiency of SO〓〓/TiO〓 was 10 times of that of TiO〓 catalyst for the photocatalytic degradation of bromomethane. Therefore, the SO〓〓/TiO〓 superacid catalyst is promising for practical application in environmental remediation.It was found that both L and B acid sites exist on SO〓〓/TiO〓 photocatalyst while only L acid sites on TiO〓 photocatalyst. On the basis of experimental results, the synergistic model of superacidic centers was proposed for SO〓〓/TiO〓 photocatalyst to explain the photocatalytic behavior and the mechanism of superacidifing effects, assuming that the adjacent L and B acid sites induced by SO〓〓 comprise cooperatively the superacidic center on superacid photocatalyst. The group cooperation of the superacidic center could strengthen the surface acidity, increase surface acid sites and the adsorbtion of O〓, promote separation of photogenerated electron-hole pair, enhance the interfacial transfer of charges and reversibility of water adsorption. Consequently the excellent photocatalytic activity, reaction stability and resistibility to humidity of SO〓〓/TiO〓 superacid photocatalyst may attributed to the group cooperated effect of the superacidic center on the photocatalyst.

研究结果表明:SO〓〓与TiO〓表面的结合为螯合式双配位结构;TiO〓光催化剂表面经H〓SO〓浸渍处理后,提高了表面酸性,改善了催化剂结构和光催化性能,当H〓SO〓浸渍浓度为1.0mol.L〓、烧结温度为450℃时,可制得SO〓〓/TiO〓超强酸催化剂(H〓<-12.14),其结构和光催化活性得到明显改善,与TiO〓相比,SO〓〓/TiO〓光催化剂的锐钛矿含量高、晶粒小、BET比表面积大、孔径分布集中、光谱吸收边蓝移,具有优异的光催化氧化活性、稳定性及抗湿性能,光催化降解溴代甲烷的表观量子效率比TiO〓催化剂提高了一个数量级,是一种有实际应用前景的高效光催化剂;由此提出了SO〓〓/TiO〓超强酸催化剂表面集团协同作用的超强酸中心模型,认为在SO〓〓/TiO〓超强酸催化剂表面,由SO〓〓诱导的相邻L酸中心和B酸中心组成了集团协同作用的超强酸中心,其集团协同作用显著地增强了催化剂表面酸性、增大了表面酸量及O〓吸附量、促进了光生电子和空穴的分离及界面电荷转移,具有可逆吸附水的性能,是SO〓〓/TiO〓超强酸催化剂具有优异的光催化氧化活性、很好的活性稳定性及抗湿性能的重要原因。

The chlorophyll contents and photosynthesis decreased gradually with the increasing of Cu2+ concentration. The respiration rose gradually in the range of 0.01~10 mg/L Cu2+ and fell gently over 10 mg/L. These results indicated that Chlorococcum sp.

在1 mg/L Cu2+浓度下,绿球藻对Cu2+的去除率最高为90.5%;叶绿素含量及光合作用强度随Cu2+浓度的升高逐渐降低;呼吸强度在0.01~10 mg/L Cu2+浓度范围内逐渐升高,大于10 mg/L Cu2+则逐渐降低。

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