激活

FN and LN (the non-collagenous index) out of ECM were measured by immuno-histochemistry mean, and the accumulation of ECM was measured by typeⅠand Ⅲ collagen ,α-SMA was chosen as a symbol of the activated reposit fat cell. TGF-β〓 was chosen as a symbol of the cellular factor made the reposit fat cell activated. We observed the mechanism of 286 through the variety of the upper indexes during the experiment.

用免疫组化方法测评肝细胞外基质中的非胶原指标FN、LN，胶原指标Ⅰ、Ⅲ型胶原等在实验过程中的变化作为判定ECM沉积增多的事实指标；用a-平滑肌肌动蛋白作为贮脂细胞被激活的标志物指标；用转化生长因子-β〓作为激活贮脂细胞的细胞因子指标；通过观测上述指标在实验中的变化，来探讨"268方"的作用机理。

FN and LN(the non-collagenous index) out of ECM were measured by immuno-histochemistry mean, and the accumulation of ECM was measured by type I amd III coHagen, a -SMA was chosen as a symbol ef .the activated reposit fat cell.TGF- P1 was chosen as a symbol of th ieccellular factor made the reposit fat cell activated.We observed the mi sclnanism of 286 through the variety of the upper indexes during the experiment.

用免疫组化方法测评肝细胞外基质中的非胶原指标FN、LN，胶原指标Ⅰ、Ⅲ型胶原等在实验过程中的变化作为判定ECM沉积增多的事实指标；用a-平滑肌肌动蛋白作为贮脂细胞被激活的标志物指标；用转化生长因子-β_1(TGF-β_1)作为激活贮脂细胞的细胞因子指标；通过观测上述指标在实验中的变化，来探讨"268方"的作用机理。

So we propose that before the precursor is cleaved into DG and mediator, it is released from plasma membrane first, through activating some kind of enzyme by insulin or PIPLC; meanwhile, only insulin can activate the resynthesis mechanism of the precursor, in the contrast, PIPLC was inactive at this course.

推测：胰岛素或PIPLC作用于完整细胞或膜时，激活了某种酶，使前体先从膜上释放至胞外，再被水解为介体和DG，同时胰岛素还能激活再合成前体的机制，而PIPLC却不能。

The biocatalyzed characters of the purified cellulases were investigated with the CMC-Na as substrate. The most appropriate catalyzed temprature for cellulase 1 is 60 "C,and 65 for cellulase 2. The two enzymes have the extreme stability at the temperatures no more than 50.The CMC-Na has the protective effect on the cellulase. The pH stability range of cellulase 1 is 4 ~ 8, and 6-9 for cellulase 2. Zn2+, Ca2+, Mg2+, K+, Li+can ativate cellulase 1. K+, Li"1 can ativate cellulase 2. Cellulase 1 can mainly decompose CMC and salicin. Cellulase 2 can decompose not only CMC and salicin, but other substrates feebly.

以羧甲基纤维素为底物时，酶1的最适催化温度为60℃，酶2的最适催化温度为65℃，在50℃以下稳定性较好，底物对酶有较强的保护作用；酶1和酶2的最适pH分别为5.5和5.5～6.0，酶1的pH稳定性范围为4～8，酶2的稳定性范围为6～9；Zn~(2+)，Ca~(2+)，Mg~(2+)，K~+，Li~+对酶1有激活作用，K~+，Li~+对酶2有激活作用；酶1主要对CMC和水杨素有分解作用，对其它底物几乎不分解；酶2除了可以分解CMC和水杨素外，对其它底物也有微弱的分解作用。

Yet, in the temperature range of 700-750℃, the deformation activation energies were much higher than the self-diffusion activation energy of grain boundary.

在850℃变形激活能与晶界自扩散激活能十分相近，表明晶界扩散控制的晶界滑动是超塑性变形的主要机制。

At the temperature range of 800～850℃, the deformation activation energy was very close to self-diffusion activation energy of grain boundary, which shows the main deformation mechanism is grain boundary sliding controlled by grain boundary diffusion.

在850℃变形激活能与晶界自扩散激活能十分相近，表明晶界扩散控制的晶界滑动是超塑性变形的主要机制。

And the integral sensitivity and spectral response performance parameters of the GaAs photocathode after high-temperature activation and low-temperature activation were compared.

计算并比较了高温激活和低温激活后阴极的积分灵敏度和光谱响应特性参数。

Two spotted spider mite feeding induced octadecanoid signaling pathway that resulted in activation of PⅠ-Ⅱ gene and expression of relative genes, further more PⅠ-Ⅱ protein were accumulated.

二点叶螨对番茄植株的捕食激活了脂肪酸途径，导致PI-Ⅱ基因的激活，从而诱导PI-Ⅱ蛋白的积累及相关基因的表达。

A new algorithm is proposed for identifying active subnetwork by considering both difference and correlation of gene expression profile.

提出一种融合表达谱差异性和相关性信息的激活子网辨识算法，能够在蛋白质相互作用网络中辨识高功能相关度的激活子网。

The complement system of teleost fish, like that of higher vertebrates, can be activated through all three pathways of complement.

正如更为高等的脊椎动物的补体系统一样，硬骨鱼类的补体系统可以通过三种补体激活途径得以激活。

With the development of highway construction, the speed of cars has been gradually increased.

随着公路的发展，汽车的车速也在不断提高。

So we basically had to develop a bond with the animal in terms of socializing with it.

所以我们就主要想通过跟它沟通的方式来建立一种良好的关系。