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The code plate is equipped with intelligence code, energy code, constitution code, ovulation conclusion table of women with normal catamenia as well as code positioning cooperation method.

8 ,其组成包括衬盘、生理周期盘、代码定位盘和标尺,生理周期盘、代码定位盘和标尺分别配装在衬盘的正、反两面,由盖拴固定在衬盘,生理周期盘的月日盘周圈设有月日相应标识,精力盘、智力盘和体力盘周圈分别设有精、智和体力生理周期循环变化标识,内圈盘依次位于相邻外圈盘标识内圈:代码定位盘的年份盘周圈设有 00-99 个年份标识,代码盘设有智力代码、精力代码、体力代码标识和月经正常女性排卵时间推算表以及代码定位操作方法;标尺为两把,分别配装在生理周期盘和代码定位盘,生理周期盘的标尺设有指示标尺线,代码定位盘的标尺设有定位代码标识框;本实用新型优生测算器结构简单,测算内容显示直观,操作简便。

Meanwhile for responding the GEELY Holding Group well the greatly GEELY strategy and obtains more resources and the development, the company reports after the GEELY Holding Group board of directors and has control over can authorize, in persisted the Shanghai culture will make the vehicle idea and in the Shanghai school intermediate automobile manufacture base localization invariable foundation increases the SMA automobile to construct the GEELY Holding Group upscale vehicle the production base, the new energy automobile and the classical vehicle type research and development base, the mold and the advanced equipment manufacturing center three big new localizations, In completes the existing SMA automobile limited company, Shanghai SMA GUORUN automobile limited company, the SMA engine company, the SMA research institute limited company, the SMA trading company, in the SMA automobile international Trading company's foundation, prepares for construction the establishment the Shanghai LTI China automobile Co., Limited and the SMA mold manufacture Co., Limited company which cooperates with English famous LTI Corporation, thus utilize GEELY Holding Group the international resources to realize the SMA automobile industry rapid development enabling SMA automobile to become China and even the world famous enterprise.

同时为更好地响应吉利控股集团的大吉利战略和得到更多的资源和发展,公司报经吉利控股集团董事会和经管会批准后,在坚持海派文化造车理念和海派中级汽车制造基地定位不变的基础增加将海华普汽车建设成吉利控股集团高档车的生产基地、新能源汽车与经典车型的研发基地、模具及先进设备制造中心的三大新定位,在做好现有海华普汽车有限公司、海华普国润汽车有限公司、海华普发动机公司、海华普研究院有限公司、海华普汽车销售公司、海华普汽车国际销售公司的基础,筹建成立和英国著名的LTI公司合作的海英伦帝华汽车部件有限公司和海华普模具制作有限公司,从而更好地利用吉利控股集团的国际化资源实现海华普汽车产业的飞速发展,让海华普汽车成为中国乃至世界的驰名企业。

The better condition synthesizing the assorted minerals of zirconolite and sphene doping neodymium is holding 30 min at 1230℃, and the better formula is nCa(subscript 1-x/2-y/4 Zr(subscript 1-y/4);Al(subscript x/2) Ti(subscript 2-x/2O7): nCa(subscript 1-x NdAl Ti(subscript 1-x)SiO5[4/(4-y)]:1. Nd(superscript 3+) can enter crystal lattices of ite and sphene. Sphene can immobilize Zr(subscript 4+), Al(subscript 3+) and Nd(subscript 3+); Zr(subscript 4+) and Nd(subscript 3+) replace Ca(subscript 2+), and Al(subscript 3+) replaces Ti(subscript 4+). Zirconolite can immobilize Al(subscript 3+) and Nd(subscript 3+) Nd(subscript 3+) replaces Ca(subscript 2+) and Zr(subscript 4+), and Al(subscript 3+) and replaces Ti(subscript 4+).

研究表明:钙钛锆石和榍石组合矿物固化体较佳的合成条件是在1230℃条件下保温30min,较佳配方的摩尔比为nCa(下标 1-x/2-y/4 Nd(下标 x+y/2)Zr(下标 1-y/4)Al(下标 x/2)Ti(下标 2-x/2) O7:nCa(下标 1-x Nd Ti(下标 1-x)-SiO5=[4/(4-y)]:1;Nd(标 3+)能够进入钙钛锆石和榍石晶格,榍石能够固溶Zr(标 4+)、Al(标 3+)、Nd(标 3+),Zr(标 4+)和Nd(标 3+)取代Ca(标 2+)位,Al(标 3+)占据Ti(标 4+)位,钙钛锆石能够固溶Al(标 3+)、Nd(标 3+),Nd(标 3+)进入Ca(标 2+)位和Zr(标 3+)位,Al(标 3+)占据Ti(标 4+)位。

2B8a was weakly reactive to neutrophils (23.72%) and negative for T cells, NK, DC, RBC and Plt. The antibody reacted to all 3 marrow CD34+ cells with an average positive rate of 39.33% while it was negative for G-CSF-mobilized CD34+ peripheral blood stem/progenitor cells (PBSC, 1.25%). Cell line analysis showed that the antibody notably reacted to three out of 4 cell lines (Raji, SMS-SB, Nalm-6 and Nall-1) with the positive rates of 98.78%, 98.61%, 94.93% respectively and weakly to one of them with 5.68% in B lineage cell lines and monoblastic cell line (U937, 67.78%) while it was only weakly positive or negative for other myeloid leukemia cell lines including Meg01 (33.40%), HL-60 (29.70%),K562 (28.19%), KG1a (16.23 %) and HEL92.1.7 (8.02%). Among 4 T lineage leukemia,5 neuroblastoma and 1 colon cancer cell lines tested, only Molt-3 was found weakly positive (31.40%) for 2B8a, while the remaining 3 T cell lines (Molt4, JM and CCRF-CEM), 5 neuroblastoma cell lines (LA-N1, KCNR, BE, SK-N-SH, SK-N-AS) and the colon cancer cell line (HR8348) tested were negative.

结果表明: 2B8a抗原在外周血B细胞表达(3/3例,平均阳性细胞数为26.29 %),而在T淋巴细胞和NK细胞不表达(0/3例);在粒细胞和单核细胞阳性表达均为2/3例,平均阳性细胞数分别是23.72 %和59.84 %;在DC细胞、红细胞和血小板均不表达(0/3例)。2B8a抗原在骨髓CD34+细胞的阳性表达是3/3例,平均阳性细胞数39.33 %,而在G-CSF动员的外周血CD34+细胞的阳性表达仅1/3例,平均阳性细胞数为1.25 %。2B8a抗原在B系细胞系Raji、SMS-SB、Nalm-6和Nall-1的平均阳性细胞数分别为98.78 %、98.61 %、94.93 %和5.68 %;在T系细胞系Molt-3的平均阳性细胞数为31.40 %,而在Molt-4、JM和CCRF-CEM 细胞不表达;在髓系细胞系U937、Meg-01、HL-60、K562、KG1a和HEL92.1.7的平均阳性细胞数分别为67.78 %、33.40 %、29.70 %、28.19 %、16.23 %和8.02 %;在神经母细胞瘤细胞系SK-N-SH、KCNR、BE、LAN-1和SK-N-AS细胞以及结肠癌细胞系HR8348细胞均不表达,而在羊膜细胞系FL细胞呈一定的阳性表达,平均阳性细胞数为45.03%。

Cell line analysis showed that the antibody notably reacted to three out of 4 cell lines (Raji, SMS-SB, Nalm-6 and Nall-1) with the positive rates of 98.78%, 98.61%, 94.93% respectively and weakly to one of them with 5.68% in B lineage cell lines and monoblastic cell line (U937, 67.78%) while it was only weakly positive or negative for other myeloid leukemia cell lines including Meg01 (33.40%), HL-60 (29.70%),K562 (28.19%), KG1a (16.23 %) and HEL92.1.7 (8.02%). Among 4 T lineage leukemia,5 neuroblastoma and 1 colon cancer cell lines tested, only Molt-3 was found weakly positive (31.40%) for 2B8a, while the remaining 3 T cell lines (Molt4, JM and CCRF-CEM), 5 neuroblastoma cell lines (LA-N1, KCNR, BE, SK-N-SH, SK-N-AS) and the colon cancer cell line (HR8348) tested were negative.

结果表明: 2B8a抗原在外周血B细胞表达(3/3例,平均阳性细胞数为26.29 %),而在T淋巴细胞和NK细胞不表达(0/3例);在粒细胞和单核细胞阳性表达均为2/3例,平均阳性细胞数分别是23.72 %和59.84 %;在DC细胞、红细胞和血小板均不表达(0/3例)。2B8a抗原在骨髓CD34+细胞的阳性表达是3/3例,平均阳性细胞数39.33 %,而在G-CSF动员的外周血CD34 细胞的阳性表达仅1/3例,平均阳性细胞数为1.25 %。2B8a抗原在B系细胞系Raji、SMS-SB、Nalm-6和Nall-1的平均阳性细胞数分别为98.78 %、98.61 %、94.93 %和5.68 %;在T系细胞系Molt-3的平均阳性细胞数为31.40 %,而在Molt-4、JM和CCRF-CEM 细胞不表达;在髓系细胞系U937、Meg-01、HL-60、K562、KG1a和HEL92.1.7的平均阳性细胞数分别为67.78 %、33.40 %、29.70 %、28.19 %、16.23 %和8.02 %;在神经母细胞瘤细胞系SK-N-SH、KCNR、BE、LAN-1和SK-N-AS细胞以及结肠癌细胞系HR8348细胞均不表达,而在羊膜细胞系FL细胞呈一定的阳性表达,平均阳性细胞数为45.03%。

The floatation rate of Pd (superscript 2+) reaches 100% when the concentrations of NaNO3, KBr and cetyl pyridinium bromide in solution are 0.05 g/mL, 3.0×10^(-2) mol/L, 5.0×10^(-4) mol/L(pH 4.0), respectively. Pd (superscript 2+) could be separated from Ru (superscript 3+), Al (superscript 3+), Cr (superscript 3+), Ni (superscript 2+), Ga (superscript 3+), Fe (superscript 3+) and Zn (superscript 2+) by floatation quantiatively. A method of flotation separation and enrichment of Pd (superscript 2+) was established.

当溶液中硝酸钠、溴化钾、溴化十六烷基吡啶的浓度分别为0.05 g/mL,3.0×10^(-2)mol/L,5.0×10^(-4)mol/L,在pH 4.0时,Pd(标 2+)的浮选率达到100%,Pd(标 2+)可与Ru(标 3+),Al(标 3+),Cr(标 3+),Ni(标 2+),Ga(标 3+),Fe(标 3+),Zn(标 2+)定量分离,据此建立了浮选分离和富集Pd(标 2+)的新方法。

MTT assay FAK signaling pathway inhibitor genistein on human corneal epithelial cell cytotoxicity;RT-PCR detection of human corneal epithelial cells adhesion to fungus at different times,extracellular matrix protein including laminin,fibronectin,FN glass,Ⅳcollagen,transmembrane protein integrinαⅤ,integrinβ1(ITGβ1),as well as the FAK signaling pathway FAK1,FAK2 and Paxillin gene expression;Western blot detection of the signal transduction pathway adhesion-associated protein ITGβ1,FAK and PAX expression and the inhibition of genistein. Immunocytochemical method was used to observe the LN,FN and FAK expression in human corneal epithelial cells during interaction with the fungues;Laser scanning confocal microscope had a cell positioning on FN,FAK and PAX,observed the changing of the human corneal epithelial cytoskeleton after stimulated by fungues;Quantitatived by flow cytometry to detect of human corneal epithelial cells with PAX at ITGβ1 fungal expression after adhesion;Optical microscopy quantitied the fungues and human corneal epithelial cell adhesion and recorded to determination the integral optical density afrer adhesion;Scanning and transmitted electron microscope observed the changing of cell ultrastructure after fungues and human corneal epithelial cell adhesion.

第一部分真菌激活人角膜皮细胞FAK信号转导通路的体外实验研究将三种常见致病真菌(白色念珠菌、烟曲霉菌和茄病镰刀菌)分别与人角膜皮细胞共孵育,MTT法检测FAK信号通路抑制剂染料木黄酮的对人角膜皮细胞的细胞毒性作用;RT-PCR检测真菌黏附人角膜皮细胞后不同时间细胞外基质层连蛋白、纤连蛋白、玻连蛋白、Ⅳ型胶原、跨膜蛋白整合素αV、整合素β1(ITGβ1),以及FAK信号通路中FAK1、FAK2和桩蛋白基因的表达情况;Western blot的方法检测黏附信号转导途径相关蛋白ITGβ1、FAK和PAX的表达,以及染料木黄酮对真菌刺激人角膜皮细胞FAK信息通路活化的抑制作用;免疫细胞化学方法观察人角膜皮细胞与真菌相互作用过程中LN、FN和FAK的表达;激光共聚焦显微镜对FN、FAK和PAX进行了细胞定位,并观察真菌刺激后人角膜皮细胞骨架的变化;流式细胞仪定量检测人角膜皮细胞ITGβ1与PAX在真菌黏附后表达的改变;光学显微镜观察真菌与人角膜皮细胞黏附数量,记录并测定了黏附后积分光密度值OD扫描及投射电镜观察了真菌与人角膜皮细胞黏附后,细胞超微结构的改变。

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According to the clear water experiment, aeration performance of the new equipment is good with high total oxygen transfer coefficient and oxygen utilization ratio.

曝气设备的动力效率在叶轮转速为120rpm~150rpm时取得最大值,此时氧利用率和充氧能力也具有较高值。

The environmental stability of that world - including its crushing pressures and icy darkness - means that some of its most famous inhabitants have survived for eons as evolutionary throwbacks, their bodies undergoing little change.

稳定的海底环境─包括能把人压扁的压力和冰冷的黑暗─意谓海底某些最知名的栖居生物已以演化返祖的样态活了万世,形体几无变化。

When I was in school, the rabbi explained everythingin the Bible two different ways.

当我上学的时候,老师解释《圣经》用两种不同的方法。