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binding course相关的网络例句

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

Results Intercalative binding and groove binding coexisted between yeast dsDNA and GM.

结果:酵母DNA和甲磺酸加替沙星之间无静电作用,插入作用和沟槽作用共存。

These results indicated that palmatine had one common binding site on the immobilizedβ_2-AR column,the association constant was 2.93×10~4 L/mol at pH 7.2 and 25℃,while jatrorrhizine had two bingding sites,the association constants at these two sites were 1.93×10~4 and 1.56×10~5 L/mol,respectively.And the molar ratio of weak bingding sites to strong binding sites was 93:7.Palmatine and jatrorrhizine had competed for low-affinity site in immobilizedβ_2-AR.

结果表明,盐酸巴马汀与β_2-AR只有一类结合位点,在流动相pH 7.2,温度25℃时盐酸巴马汀与β_2-AR的结合常数为2.93×10~4 L/mol;盐酸药根碱与β_2-AR有两类结合位点,在这两类结合位点上的结合常数分别为1.93×10~4和1.56x10~5L/mol,两类结合位点数的比值为93:7,且盐酸巴马汀和盐酸药根碱竞争低亲和力的结合位点。

Studies of the binding of metal to calmodulin and the subsequent binding of metal-calmodulin complexes to the target protein/peptide revealed that the La-content calmodulin complexes to its target exhibit similar affinity with the Ca-calmodulin complexes.However, there were substle differences in protein conformation as well as the kinetical properties between the two kinds of metal-calmodulin complexes, suggesting Ln could produce cellular effects via the Ca/calmodulin signaling systems.

稀土离子和钙调蛋白的结合以及后续和靶酶的结合,在热力学上与钙离子激活蛋白具有相同的亲合力,但在动力学性质上以及细微构象上明显不同,显示稀土离子可通过细胞钙相关信号系统产生特别的生物效应。

Considering the merits of in vivo studies in biotransformation i. e. activation or inactivation, protein-binding such as sex hormone binding protein , toxicokinetics, and more evaluative in hazard identification and risk assessment, we selected a battery of short-term and long-term in vivo studies, including uterotrophic assay in weaning mice and ovariectomized adult mice, an in vivo multiple endpoints assay, and a gestational and lactational exposure assay to identify the estrogenic effects of endosulfan on the offspring.

考虑到体内试验在代谢转化、血浆蛋白如性激素结合蛋白的结合、代谢动力学等方面比体外试验优越,在危害鉴定和危险度评定中更有价值,我们选择了多项体内试验,包括对幼年小鼠和卵巢切除成年小鼠的子宫增殖作用、对成年去势小鼠的体内多终点观察以及大鼠孕期和哺乳期接触对雄性子代生殖系统结构和功能的改变,即去雄性化或雌性化作用等,来验证硫丹的体内雌激素样作用。

The results imply that the inhibition of NADPH is due to the earlier binding of NADPH to the enzyme which caused the arm to move from the condensation domain to the reduction domain so as to affect the binding of substrate malonyl CoA and inhibit the activity.

实验结果表明:NADPH对脂肪酸合成酶的抑制可能是由于NADPH在酶上过早的结合而使该酶的活臂向远离缩合中心的方向移动,从而影响了底物丙二酰辅酶A与酶的结合,造成酶活性的下降。

The macrocyclic polyamines are a kind of excellent ligands and have a substantially high binding affinity with transition metal ions. Macrocyclic polyamine metal complexes as enzyme models are widely used in chemical biology, medicine and gene therapy. 1, 4, 7, 10-tetrazacyclododecane is a representative macrocyclic polyamines compound and shows high binding affinity with transition metal ions, such as Zn, Cu and Co. Their metal complexes especially multinuclear complexes were widely used in DNA, RNA recognition.

大环多胺化合物是一类性质独特的优秀配体,具有良好的金属配位能力,其金属配合物作为人工酶模型广泛应用于核酸结构及功能研究、基因表达与调控、抗癌药物的研制等生物、化学和医学领域。1,4,7,10-四氮杂十二烷是典型的大环多胺化合物,对过渡金属离子Zn, Cu and Co有良好的配位能力,这些金属配合物特别是多核金属配合物被广泛应用于DNA识别中。

Using 〓-SCH 23390 (0.02-2 nM) and 〓-spiperone (0.02-2 nM) as ligands bound to 〓 and 〓 receptors in rat neostriatum, Scatchard curve showed aproximately a linear relationship for both 〓-SCH 23390 and 〓-spiperone binding, indicating they labeled separate one binding site.

应用〓和〓〓与大鼠新纹状体中〓、〓受体相结合,Scatchard作图显示均接近直线,表明分别标记受体的一个结合位点。

The data display sharp resolution of binding position [+/-50 base pairs], which facilitated our finding motifs and allowed us to identify noncanonical NRSF-binding motifs.

数据显示了结合位点灵敏的分辨率(+/-50bp),使得我们寻找motif 变得容易,并允许我们确定以前未发现的 NRSF-结合motifs。

Upon binding ATP or a nonhydrolyzable analog such as AMPPNP, RecA undergoes an allosteric transition into a high-affinity DNA-binding form. When RecA combines with dsDNA to form RecA-dsDNA nucleofiliment, it can unwind dsDNA and change the dsDNA structure.

在ATP或其类似物的辅助下,RecA可以直接与双股DNA结合而形成核丝,并将双股DNA加以解螺旋,并改变双股DNA的结构。

Results: 125 I Mel binding sites in optomeninx was the most, in eptochiasm and sniff ball was next; GTPγS dose dependently inhibited the binding.

结果 :视网膜 1 2 5 I- Mel特异结合量最高,视交叉及嗅球次之,其次为下丘脑、海马、脑干;动力学分析表明 Mel与其受体的结合为可逆性结合;特异性结合分析提示对 Mel呈高度特异性;10和 5 0μm ol/ L GTPγS使 1 2 5 I- Mel特异结合降低。

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