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binding energy相关的网络例句

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

However, the binding patterns between the HU-induced and uninduced HEL cells were different. The data in Southwestern-blot analysis showed that the molecular weights of the GATA factors binding to the HS2core DNA sequence were 43kd and 47kd respectively.

反义寡核苷酸技术及RT-PCR的结果表明,GATA-1的反义核苷酸抑制了羟基脲诱导的β-珠蛋白基因的表达,进一步证明了GATA-1因子在羟基脲诱导的HEL细胞分化过程中是不可缺少的促进因素。

Biotinylated lectins:UEA-Ⅰ, RCA-Ⅰ, DBA, PSA, PNA, BSL, LCA, WGA, ConA AND SBA were used as probes to identify lectin binding sites and to determine if lectin binding patterns change with age in the developing of human fetal esopha geal epithelium (8W, 14W, 20W, 28W and 32W).

采用十种生物素化凝集素UEA-I、DBA、PSA、B SL、PNA、LCA、RCA-I、SBA、ConA及WGA分别对8W、14W、20W 28W及32W的人胎儿食管上皮进行研究,以确定胎儿食管上皮在发育过程中凝集素的结合位点以及结合方式随年龄的变化。

METHODS: Cytometry and soft agar were employed in observing the biological characters of MEC-1 and Mc3 cell strain. The expressions of the two sub-types of MEC-1 and Mc3 cell strain, SSTR1 and SSTR2, were detected by hybridization in situ. The condition of the binding between MEC-1, Mc3 and 125I-RC-160 was analyzed by radioactive genin binding analysis.

采用细胞计数法、软琼脂法等观察MEC-1及Mc3细胞株生物学特性;以原位杂交法检测MEC-1,Mc3细胞株SSTR1及SSTR2两种亚型的表达情况;以放射配基结合分析法分析MEC-1,Mc3细胞与125I-RC-60的结合情况。

The results showed that though apoHb could be reconstituted with all FePs, it showed different functions. Binding of apoHb with hemin can enhance the heterolytic cleavage of O-O bond of H〓O〓, but inhibiting the cleavage when FeTCPP and FeTPPS〓 were used instead of hemin. The binding of apoHb with FeTTMAPP showed negligible influence on the cleavage of O-O bond in H〓O〓.

结果表明,虽然具有阴离子基团的FeTCPP和FeTPPS〓能够在天然血红蛋白中辅基位置的附近与脱辅基血红蛋白结合,但是由于结构上与天然辅基的差别,使得血红素蛋白中相应的氨基酸残基不能起到有效的作用,因此不但不能提高反而抑制了其过氧化物酶活性;而对于具有阳离子基团的FeTTMAPP,脱辅基血红蛋白对其活性没有明显的影响。

For example the whole book visions of luxury and bookbiding or heterotype or sewing binding or binding hardcover and air back processing without plugging a soft cloth hardcover, etc.

例如整书装订方式出现的豪华装、异型装、无线胶订或锁线胶订精装、空背加工不黏堵布的软精装等。

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。

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