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After the \4ear resist alloy with high melting point is sprayed on the prototype , the spray formed layer is backupped, the prototype is separated from the spray layer , the post processing is completed, and a high precision perdurable metal tool is finally produced.

在该原型表面熔射高熔点耐磨合金后,通过对熔射层背衬补强、并将原型与熔射层分离以及后处理,即可制得高精度耐久金属模具。

After the \4ear resistant alloy with high melting point is sprayed on the prototype, the spray formed layer is backupped, the prototype is separated from the spray layer, the post processing is completed, and a high precision perdurable metal tool is finally produced.

在该原型表面熔射高熔点耐磨合金后,通过对熔射层背衬补强、并将原型与熔射层分离以及后处理,即可制得高精度耐久金属模具。

Urogenital swabs were inoculated on the conventional solid media, new solid media and urea liquid media as such.⑤Synovial fluid, synovial-membrane biopsy samples, blood, urogenital swabs and pharyngal swabs from RA were examed the presence of mycoplasmas using culture and Polymerase Chain Reaction assay.

46例泌尿生殖道标本直接划在固体培养基表面后洗脱在Uu液体培养基和Mh液体培养基中;另20例标本直接划在无青霉素的固体培养基后洗脱在Uu液体培养基中。

The induced hmscs-tert were examined by oil red-o staining, alkaline phosphates staining and von kossa staining. results the hmsc-tert was negative for cd34, cd45, cd44, cd106 and cd166. after the induction, accumulated cytoplasmatic red lipid droplets were clearly visible in the adipose cells by oil red o staining, and alkaline phosphates-positive pitchy grains formed in the intracytoplasm and calcium nodes were found by von kossa staining in the osteoblasts.

结果 hmsc-tert细胞表面抗原检测cd34、cd45、cd44、cd106、cd166均为阴性;脂肪细胞定向诱导后油红o染色见胞浆内有红色脂肪颗粒,成骨细胞定向诱导后见胞浆内有碱性磷酸酶染色阳性黑褐色颗粒,von kossa染色见有钙结节形成。

RESULTS: Both resting B cells and T cells did not express PD-L1 on their surface, however PD-L1 expression was significantly up-regulated on the surface of the activated B cells after 6 h stimulation with LPS or pokeweed mitogen, and the percentages of B cells that expressed PD-L1 reached a plateau at 24 h, which were (46.26±10.71)% with LPS and (43.67±6.14)% with PWM stimulation, respectively. No markedly change of PD-L1 expression on the surface of the activated T cells after stimulation with LPS was observed, but upregulation of PD-L1 expression was observed when stimulation with PWM.

结果: 静息B细胞和T细胞表面不表达PD-L1,LPS和PWM刺激6 h后表达PD-L1的B细胞百分率均显著高于静息B细胞,24 h达到最高,分别为(46.26±10.71)%和(43.67±6.14)%,之后随时间延长而降低;表达PD-L1的T细胞百分率在LPS刺激下无显著变化,但PWM刺激6 h后百分率明显高于静息条件,24 h达到最高,为(25.42±9.23)%,之后下降。

In order to overcome this problem, in this paper, the surface electric current of the conducting sea surface and the first-order scattering from the conducting plate are obtained by employing Physic Optics method. The backscattering field of the time-dependant sea surface is calculated by using Kirchhoff Approximation. Meanwhile, taking the advantage of a newly developed technique that utilizes the reciprocity theorem, the difficulty in formulating the secondary scattered fields from the composite target is reduced. The dependences of the backscattered field on the parameters, such as the wind speed and the sizes of the plate are discussed.

为了克服这一问题,本文应用物理光学近似求解了导体海面表面电流及导体平板的一阶散射场,应用基尔霍夫近似给出了海面的后向散射场,同时借助互易性定理降低了求解平板和海面之间二次耦合散射场的难度,讨论了平板尺寸、风速等对后向复合散射场的影响。

The curvature of the roofline is drastically accelerated towards the back-end so that the back-end roof surfaces are floating into each other.

曲率的roofline是大幅加快对后端,使后端屋顶表面的浮动相互转化。

It is made from parent metal resin, dimming powder and solvent, spray on glass surface and form film similar to sandblast and medicine glass and more colors will appear after color essence is added.

有成膜树脂,消光粉和溶剂组成,喷涂于玻璃表面后形成一层类似喷砂,药水砂玻璃效果的漆膜,加入色精调色后有更多的色彩效果。

The transverse cervical artery which crosses the anterior scalene muscle covers the part of the tumor and lies superficially.

而臂丛神经鞘瘤位于颈动脉分叉水平以下,紧贴前斜角肌后或后外方,颈横动脉横跨前斜角肌表面向肿瘤未被肌肉覆盖部分的浅面走行。

METHODS: The rib trabeculae were resected and broken, trypsinizated and washed completely by PBS. Bone surface and non-adhesive floating cells in cleaning fluid were observed with inverted microscope. Rib trabeculae was washed by DMEM culture medium once, and cultured in culture bottle. The culture liquid was replaced by new one once a week. The osteoblast was moved from the sclerite a week later. The cells were fused monolayer and could be subcultured 4 to 6 weeks later.

切下人肋骨骨小梁剪碎,胰酶消化后以PBS彻底冲洗直至于倒置显微镜下观察骨片表面及清洗液中无粘着及漂浮的细胞,以DMEM完全培养液清洗骨小梁1次,移入培养瓶内培养,每周更换培养液1次,1周后可见成骨细胞自骨片移出,4~6周细胞融合成单层可作传代培养。

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