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Version 1.61 added recognition of AGEIA PhysX accelerator card, added synchronization with other sysinfo/monitoring tools in order to avoid collisions, fixed interpreting of PnP node 32-bit memory resources, enhanced support of VIA C7 and added recognition of C7-M and Eden processors, recognition of Intel 3000/3010 (Mukilteo-2/2P) chipsets, preliminary recognition of Intel Crestline chipset.

在新的版本中加入了对ATI RS350M、M18的支持;增强了对Intel 915、925和E7525芯片组的支持;加入了对LGA775平台的识别能力;加入了对AMD Sempron的支持;加入了对Trident/XGI Volari-XP5的支持;针对NV4X和ATI R4xx更新了GPU/Mem clock calculation;针对i915、i925和ICH6芯片组合增加了更多信息的显示;新版本还加入了对Winbond W83647HF硬件监视器的支持;增强了对VIA KT880芯片组的支持…… XHoy

Methods The inter-leukin2activity was observed by MTT colormietric assay,the interleukin2receptor expression of lymphocyte mem-brane was examined by immunofluoresence technique and lymphocyte blastogenesis in peripheral blood was measured by morphologic observation.

通过体外实验,运用MTT比色法、免疫荧光技术、淋巴细胞转化试验等实验方法,检测白细胞介素2活性、淋巴细胞膜白细胞介素2受体含量及外周血淋巴细胞转化功能。

A successful operation clears the carry flag and allows a program to allocate mem- ory from it.

一个成功的手术清除携带国旗,并允许一个项目,拨出膜 ory从它。

The invention is directed a patterned contact sheet and to a method of bonding a cover wafer to an interposer wafer using the patterned contact sheet having a waffle-like pattern of a plurality of ridges and plurality of wells to form a cover/interposer combination or unit that can be bonded to a substrate having a MEMs device thereon, the cover wafer, interposer wafer and substrate together forming a protective packaging for the MEMS.

本发明涉及在制造过程中保护临界表面的形成有图案的接触片材以及一种使用形成有图案的接触片材将盖子片粘合到插入物片上以形成盖子/插入物组合或单元的方法,所述接触片材具有华夫饼干状图案的许多脊和许多井,所述盖子/插入物组合或单元可粘合到具有MEM设备的基材上,所述盖子片、插入物片和基材一起形成MEM用的保护性封装。

Methods: M-CSF-dependent bone marrow cells were isolated from 5-6 weeks old mice, and cultured in the presence of MCSF (25μg/L) with different concentrations of TNF-α(0, 1, 10, 100 μg/L) for 5 days, the formation of TRAP multinucleated cells was observed. These cells were also cultured in the presence of both RANKL (30 μg/L) and M-CSF (25 μg/L) with or without 10 μg/L TNF-α for4, 5, 6 and 9 days. The number of TRAP multinucleated cells and resorption pits on dentine slices were counted under light microscope.

选用小鼠巨噬细胞集落刺激因子依赖性非附着性骨髓细胞,在含有25μg/L M-CSF和0,1,10,100μg/L TNF-α的α-MEM培养液中培养5d后,观察抗酒石酸酸性磷酸酶染色阳性多核细胞的形成;细胞在含有25μg/L M-CSF和30μg/L sRANKL的α-MEM培养液中进行培养,比较加入和不加入10μg/L TNF-α培养4、5、6和9d后,所形成的TRAP多核细胞的数目和骨吸收面积。

Methods: M-CSF-dependent bone marrow cells were isolated from 5-6 weeks old mice, and cultured in the presence of M-CSF (25 μg/L) with different concentrations of TNF-α(0, 1, 10, 100 μg/L) for 5 days, the formation of TRAP multinucleated cells was observed.

选用小鼠巨噬细胞集落刺激因子依赖性非附着性骨髓细胞,在含有25μg/LM-CSF和0,1,10,100μg/LTNF-α的α-MEM培养液中培养5d后,观察抗酒石酸酸性磷酸酶染色阳性多核细胞的形成;细胞在含有25μg/LM-CSF和30μg/LsRANKL的α-MEM培养液中进行培养,比较加入和不加入10μg/LTNF-α培养4、5、6和9d后,所形成的TRAP多核细胞的数目和骨吸收面积。

The results showed that the metabolizable energy for maintenanceand erude protein for maintenace of the clucks on the average were 925.82KJ/W0.75/d,10.200.7g/W0.75/d in 1st to 21th day of age and 884.52KJ/W0.75d.8.23g/W0.75/d in 22th to 49th day of age,respectively.

结果表明,樱桃谷肉鸭的平均维持代谢能和维持粗蛋白的需要量是:1~21日龄MEm=925.8 KJ/W~(0.75)/d,CPm=10.2g/W~(0.75)/d:21~49日龄MEm=884.5 KJ/W~(0.75)/d,CPm=8.2g/W~(0.75)/d。

But interestingly, this proliferation activity was not observed in 10% NCS-MEM or 4% BSA-serum free MEM.

有趣的是sOGP在体外的成骨活性作用必须有血清白蛋白和血清中某些因子的参与。

However, when two maturing oocytes fused and two spindle will form in the big cell, the chromosomes will not intermingle. In the present study, we removed GV from one oocyte and transfer to the perivetelline space of another GV oocyte. After fusion the resulting oocytes which contained two GVs were cultured further in MEM.

在本实验中,我们利用小鼠GV期卵母细胞将一枚卵母细胞的生发泡取出后移至另一未经去核处理的GV期卵母细胞透明带下,经三次电脉冲作用后将融合的含有两个GV的卵母细胞放入MEM成熟培养液中培养,在培养成熟的不同阶段分别收集卵母细胞进行免疫荧光染色观察微管及核的变化。

The results showed that after 2 h of culture in MEM the chromosomes of oocyte were seperated to form telophase I while a small spindle was observed around chromosomes of primary spermatocyte. However, two clear spindles were observed in the oocytes cultured in CB containing MEM. After further culture, the chromosomes of both primary spermatocyte and oocyte intermingled and formed one large spindle.

在无CB的培养液中培养的卵母细胞培养2小时后,卵母细胞已经进入第一次减数分裂的后期,染色体开始被拉向两极,而精母细胞的MI纺锤体才刚刚形成,虽然继续培养两者染色体可以合二为一并形成一个纺锤体,但是有些染色体发生滞后;当卵母细胞在含有CB的培养液中培养2小时后,在卵母细胞内形成两个相似大小的MI纺锤体,进一步培养形成一个大的纺锤体,染色体正常。

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