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For pre-selection of iron compounds that ferrous sulfate, ferrous chloride, ferrous fumarate, carbonyl iron, amino acid chelated iron, iron asporotate, fenic chloride and ferric pyrophosphate were added in reconstituted skim milk to undergo in vitro digestion, respectively, and then the selected iron compounds were added in reconstituted whole milk to compare the iron bioavailability by estimating dialyzable ferrous iron, dialyzable total iron, nondialyzable and total ferrous iron, respectively.

取硫酸亚铁、反丁烯二酸亚铁、氯化亚铁、艰基铁、Iron asporotate、Amino acid chelated iron、氯化铁与焦磷酸铁等不同铁剂添加於脱脂还原乳中进行体外消化试验，並筛选生物利用性佳之铁剂分别添加於全脂还原乳中，以可透析二价铁、可透析总铁、未透析二价铁及总二价铁等作为评估之指標。

On the silicon substrate an epitomical layer is made,where IC components are formed subsequently.In an CVDprocess,the silicon substrates places in a vacuum crystal tube are first heated to 1,600°C by high-frequency radio power and then H⒉Cl⒉Si and certain gaseous compounds of As or P is injected into the tube to make a deposit of several um on their surface.Ions of As or P are impurity deliberately added to the singl-crystalline silicon structure to supply electrons that transmit "negative"current in the silicon crystals,which is called n-type silicon.Bcan be added as impurity to produce p-type silicon that supplies holes for transmitting "positive"current.Whether a p--type of an n-type silicon substrate is needed depends on what type of transistors is expected to be manufactured on it:n-p-n type of p-n-p type

对硅衬底上的一个epitomical层了，而IC零件形成subsequently.in一个CVD法（化学气相depsition ）过程中，硅衬底的地方在真空晶体管均先加热至1600 ° C时，由高频率的无线电功率，并然后h ⒉氯⒉硅和某些气态的化合物，砷或P ，是注入试管，使存款的几位嗯对他们surface.ions的作为或P是杂质刻意添加到单结晶硅的结构，以供应电子传递的&负面&目前，在硅晶体，即所谓N型silicon.b ，可以增加一条，作为杂质产生的p型硅供应孔转递&积极& current.whether一个P -类型的一个n型硅衬底，是需要靠哪些类型的晶体管预计将在制造上它： NPN型的PNP型

Both the HepG2 cells and L-O2 cells have the expression of RhoA protein. However, the expression level of RhoA in HepG2 is much higher than that in L-O2. we also discover that the number of HepG2 cells mults more greatly with the detection of Millicell cabin than that of L-O2 cells through the hole, and that the number of HepG2 cells mults obviously and predominantly if added to RhoA excitomotor and decreases, obviously if added to RhoA antagon.

RhoA蛋白在HepG2及L-O2两株细胞中均有表达，但肝癌细胞株HepG2的表达量远远高于正常细胞株L-O2；通过Millicell小室检测，发现HepG2细胞通过细胞小室虑孔的细胞比L-O2细胞明显增多；HepG2细胞在加入RhoA激动剂后通过细胞小室虑孔的细胞显著增多；HepG2细胞在加入RhoA拮抗剂后剂通过细胞小室虑孔的细胞显著减少。

Although the added value of this product is very high, but vendors are actual production is very difficult to achieve high added value, because the class labels in addition to business card printing and membership card equipment, filmogen it is required, you need to resolve two outstanding technical challenges: one is to eliminate static electricity, or high-speed cutting.

这栽产物虽然附加值出格矮，但是厂家在本质出产洋却很难达成矮的附加值，来因不离是，该类标签不兴了差制卡和会员卡制息摆设、薄膜质料有请求之外，还必给处置两个出色的技艺艰难：一是打消静电，二是矮速模切。

Although the added value of this product is very high, but vendors are actual production is very difficult to achieve high added value, because the class labels in addition to business card printing and membership card equipment, filmogen it is required, you need to resolve two outstanding technical challenges, a 1.2 is to eliminate static electricity was high speed die-cutting.

这栽产物虽然附加值出格矮。但是厂家在本质出产洋却很难达成矮的附加值，来因不离是，该类标签不兴了差制卡和会员卡制息摆设、薄膜质料有请求之外，还必给处置两个出色的技艺艰难，一是打消静电。二是矮速模切。

The molecular sieve is prepared in the steps: at the room temperature, hexadecyl trimethyl ammonium bromide is mixed and dissolved with the sodium hydroxide, and is added with TEOS in dropping way, and simultaneously added with Me metal salt water solution and lanthanum nitrate solution in dropping way; the pH value of the mixed solution is adjusted by acetic acid to be 10 to 11, and is mixed for 1 to 2 hours after being stabilized; the sol is moved into a polyfluortetraethylene bottle to be heated and crystallized for 2 days in the oven at the temperature of 100 DEG C; after filtering, washing and drying for nights, and being calcined in a muffle at the temperature of 550 DEG C for 3 to 7 hours, the dual-metal-atom improved MCM-41 mesoporous molecular sieve is obtained.

该分子筛的制备为室温下，将十六烷基三甲基溴化铵和氢氧化钠混合溶解，搅拌并滴加入TEOS，同时滴加入Me金属盐水溶液和硝酸镧溶液并搅拌，用乙酸调节pH值至10～11，稳定后搅拌1～2小时，溶胶转入聚四氟乙烯瓶中在100℃下烘箱水热晶化2天，经过滤、洗涤、干燥过夜，马弗炉550℃焙烧3-7h，得双金属原子改性MCM-41介孔分子筛产品。

During the intermissive fed-batch process, the feeding medium was added 10 times separately to make the total amount of C and N sources equal to those added in the batch process, and the yield of maduramicin was improved to 9645 μgmL^(-1), which is 15.7% higher than that obtained during the batch process. In the continuous fed-batch process, the maduramicin yield reaches 10328 μgmL^(-1), which is 6.0% higher than that obtained in the intermissive fed-batch process, and is 29.4% higher than that obtained in the batch process.

在间歇补料分批发酵工艺中，分10次补加培养基，使碳、氮源的总浓度与分批发酵相同，马杜霉素发酵单位提高到9645μgmL^(-1)，比分批发酵提高了15.7%；在连续补料分批发酵工艺中，马杜霉素发酵单位可达10328μgmL^(-1)，比间歇补料分批发酵提高了6.0%，比分批发酵提高了29.4%。

For example, when the added concentration was 0.04%, after heating for 8 days at (55±1)℃, the POV of teaseed oil added BHA, D-isoascorbic acid, ascorbyl laurate and D-isoascorbyl laurate were 66.6, 53.8, 35.0 and 20.6 meq/kg, respectively.

当添加量为油重的0.04%、在(55±1)℃下进行强氧化试验8d后，添加BHA、异V、V月桂酸酯和异V月桂酸酯的茶籽油的过氧化值分别为66.6、53.8、35.0和20.6 meq/kg。

In early November he was repeating an experiment with one of Lenard's tubes in which a thin aluminium window had been added to permit the cathode rays to exit the tube but a cardboard covering was added to protect the aluminium from damage by the strong electrostatic field that is necessary to produce the cathode rays.

在1895年伦琴正在调查外部影响的各类真空管设备，仪器由海因里希赫兹，约翰希托夫，威廉克鲁克斯，尼古拉特斯拉和菲利普冯勒纳德，放电时，是通过他们。 [ 7 ]在11月初他是在重复实验之一勒纳德的管道，其中一个薄铝窗口增加了允许退出阴极射线管，但纸板覆盖增加了保护铝损坏的强烈静电场是必要的生产阴极射线。

When reached logarithm growth phase, it was poured or the medium was removed. 5 mL medium containing 10 mg/L mitocin-C was added , kept at 37 ℃, and then cultured in saturated humidity warm box with the CO2 of 0.05 fraction volume for 2 or 3 hours. It was coated with 0.1% gelatin in 6-hole plate, laid for over 30 minutes, and then threw away or the medium with mitocin-C was removed, washed with phosptat buffer for 5 times so as to remove the mitocin-C. 2 mL 0.05% trypsin digestive cells were added, and it was observed under microscope. When crevice appeared, cells became round (about 2－4 minutes), digestion was stopped by adding medium of the same volume, and blew up with straws repetitively to make it into monoplast suspension. Special-used cover glass was put in the center of cell counting chamber. Cells were sucked in by glass siphon, and cell suspension flew out at bucket of up or down-sides of counting chamber, until the cover glass was filled with fluid. Living cell were inoculated at concentrations of 3×108, 5×108, 1×109 L－1 after their number counted.

选取2～5代的小鼠胚胎成纤维细胞，待其至对数生长期倒掉或吸掉培养基，加入含10 mg/L丝裂霉素C的细胞全培养液5 mL，置37 ℃，体积分数0.05的CO2饱和湿度温箱中培养二三小时，在6孔板中加入0.1%明胶包被，放置30 min以上，倒掉或吸掉含丝裂霉素C的培养基，磷酸盐缓冲液清洗5遍，尽量除去丝裂霉素C，加入2 mL 0.05%的胰蛋白酶消化细胞，镜下观察，当细胞间出现裂隙，细胞变圆时（约2～4 min），立即加入等量的全培养液终止消化，并用吸管反复吹打，使之成为单细胞悬液，在细胞计数板中央放置专用的盖玻片，用玻璃虹吸管吸取细胞，让虹吸管在盖玻片上或下侧的计数板凹槽处流出悬液，至盖玻片下被液体充满为止。

The changes of the HAF after liver injury may be related to the volume of blood loss, the intraabdominal pressure and the pneumoperitoneum duration.

肝撞击伤伴失血后肝动脉血流量的变化与失血量、气腹压力以及气腹持续时间等有密切联系。

Reneging on our commitments to the world's poor cannot be an austerity measure, she said.

放弃我们给世界上的穷国的承诺不能成为一种紧缩措施。