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serum-disease相关的网络例句

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与 serum-disease 相关的网络例句 [注:此内容来源于网络,仅供参考]

Results In HFRS cases from febrile stage to polyuric stage,serum levels of TNFα、IL-1β、IFNγ、IL-2、E-selectin、L-selectin and ICAM-1 were significantly increased as compared with control group( P <0.05~0.01),on the contrary, serum IL-4 and TGFβ-1 were significantly decreased and the IFNγ/IL-10 ratio was remarkablely elevated at the same time, though serum IL-10 level was higher than normal values.

结果 从发热期至多尿期,血清TNFα、IL-1β、IFNγ、IL-2、E-选择素、L-选择素和ICAM-1水平均高于对照组, P <0.05~0.01,而IL-4、TGFβ-1则显著降低,血清IL-10虽有所增加,但其增幅远比IFNγ为低,以致IFNγ/IL-10比值显著增高;TNFα、INFγ与BUN呈一致性变化趋势,而与血小板变化趋势相反。

METHODS: Bone marrow was sterilely separated from human. After heparinization, human BMSCs were harvested using density gradient centrifugation and adherence method. At the fifth passage, BMSCs at 1×108/L were incubated in the 6-well plate and divided into 2 groups. BMSCs in the edaravone group were 50% confluent and incubated in L-DMEM containing basic fibroblast growth factor and fetal bovine serum for 24 hours. After washing in PBS, these BMSCs were incubated in serum-free L-DMEM containing 20 mg/L edaravone for 24 hours. BMSCs in the blank control group were incubated in L-DMEM, supplemented with 10% fetal bovine serum.

无菌抽取的骨髓经肝素化后,采用密度梯度离心法及贴壁筛选法分离获得人骨髓间充质干细胞,传至第5代按1× 108 L-1接种于6孔板内,设立2组,依达拉奉组细胞达50%融合时用含碱性成纤维生长因子、胎牛血清的L-DMEM预诱导24 h,PBS洗涤后再用20 mg/L依达拉奉无血清L-DMEM诱导24 h;空白对照组始终用含体积分数为10%胎牛血清的L-DMEM培养,不加任何预诱导剂和诱导剂。

2DRG co-cultured with sciatic nerve undergoing Wallerian degeneration for 14days in vivo in serum free DMEM/F12,1sciatic nerve segment was added into co-culture system at the first moment,the axons were strong and straight and could adhered to each other,and the number of axons dramatically reduced compared with that of DRG cultured alone in serum free medium.2DRG cultured in serum free DMEM/F12for 4days,then the sciatic nerve segment was added into the culture system for 3days,the axons became straight and part of them adhered to each other.

分别在无血清和有血清的条件下将新生鼠的背根神经节和体内变性14天的大鼠坐骨神经段进行联合培养作为实验组,并以在相应条件下单独培养的DRG的轴突的生长情况作为对照组来观察比较轴突的生长情况。

Their hypolipidemic effects were investigated with normaland alloxan induced diabetic mice models. In normal mice group administrating 250mg/Kg/day s. c. injection for 8 days, clofibrate preparations almost significantly decreased serum level of triglyceride; furthermore, administrating 500mg/Kg/dayfor 8 days, whole preparations significantly lowered serum level of triglyceride andpartialy lowered serum level of cholesterol.

以正常及以Alloxan诱发糖尿病雄性小鼠为试验模式,评估制剂的降血脂效果:各制剂皮下注射250mg/kg/day 8日,大都能显著降低正常小鼠的三酸甘油脂的含量;同法给与500mg/kg/day 8日,则全部都有降低三酸甘油脂的含量,且也有部分降低胆固醇的效果。

After the rats were orally administered with 0.066 4 g/, 0.134 g/, 0.4 g/ lycopene and the oil for 30 days, the concents of serum MDA, the energy of serum SA, the energy of serum GSH-Px and the contents of lipofasciin in liver were observed.

各组大鼠分别经口灌胃给予0.066 4 g/?0.134 0g/?0.400 0 g/的番茄红素及食用油30天后,测定血清中MDA含量?超氧化物歧化酶活力?谷胱甘肽过氧化物酶活力?

Compared with these of fat-fed group, the body weight, blood glucose levels after oral glucose and the glucose area under curve, 40min and 90min blood glucose levels after insulin injection subcutaneously and the glucose area under curve in the insulin tolerance test, the fasting serum insulin, insulin resistance index, serum cholesterol, triglyceride and lower density lipoprotein cholesterol decreased, the fasting serum leptin, high density lipoprotein cholesterol and C18:2 were significantly increased in N-6 PUFAs group.

n-6脂肪酸组从第1~10周体重均较高脂组明显减轻,糖负荷后血糖和糖耐量试验中葡萄糖曲线下面积、皮下注射胰岛素后40min、90min血糖及胰岛素耐量试验中葡萄糖曲线下面积、血清胰岛素、胰岛素抵抗指数、血清胆固醇、甘油三酯和低密度脂蛋白含量均较高脂组明显降低;血清瘦素水平、高密度脂蛋白、18碳2烯酸较高脂组明显升高。

Rabbit was immunized by the conjugated alginate-BSA (1.0mg/kg) for 40-days routine immunity method; ELISA method was used to examine the titration of anti-alginate serum; The first generation parotid acinar cells were chosen to divided five groups (group A :contrast, group B: BAS, group C: alginate, group D: anti-alginate serum, group E: alginate +anti-alginate serum), We examined the proliferation of each part by MTT method at four times (lh, 6h,12h and 24h); In the meanwhile, The growth and shape of parotid acinar cells were observed under phase contrast microscope and scanning electron microscope.16 of the immunized rabbits by alginate were divided equally into Al and Bl groups, 12 normal rabbits were divided equally into A2 and B2 groups as control groups, Each rabbit was affused by 0.3ml(40fil/ml)alginate though parotid duct once time two days.

将藻酸盐与BSA偶连形成具有较强免疫原性的Alginate-BSA交联物免疫兔,按抗原量1.0mg/kg接种于新西兰白兔皮内,间隔10d加强免疫1次,共加强4次后,利用间接ELISA法检测藻酸盐抗体效价:将原代培养的兔腮腺腺细胞按10~4个/ml接种到96孔板上,置入细胞培养箱继续培养3d,分为5组:A空白对照组、B牛血清白蛋白组、C藻酸盐组、D抗藻酸盐血清组和E抗藻酸盐血清+藻酸盐组,分别加入PBS、牛血清白蛋白、藻酸盐或新鲜抗藻酸盐血清继续培养,分别于1h、6h、12h和24h不同的时间点,取出96孔培养板,采用MTT法检测5组腮腺腺细胞增殖情况

Methods 34933 serum samples were screened by ELISA method on Treponema pallidum antibody. The samples with probable positive result were retested by toluidine red unheated serum test and Treponema pallidum particle assay. Results There were 559 serum samples with probable positive result.

对34933例标本采用酶联免疫吸附试验进行梅毒螺旋体的初筛,初筛结果为可疑阳性的样本进行梅毒螺旋体明胶凝集试验和甲苯胺红不加热血清反应素试验的检测。

Serum sodium 126–135 mmol/l, normal serum creatinine. Continue diuretic therapy but observe serum electrolytes.

推荐 血清钠126~135 mmol/l,血肌酐正常:继续利尿治疗不过要注意观察血电解质。

We collected Leishmania promastigotes,washed its with 0.01mol/LpH7.2 buffers ,smashed its,and then measured protein content and titrated work concentration.2.We tested Kala-azar patients"serum and healthy persons"serum of epidemic area by ELISA. The results of three antigensmethods were the same, work concentration of serum was the same(l :100).Results:The protein content of three antigens is, 901 strain with 1000ug/ml,801 strain with 960ug/ml and 951 strain with 1100ug/ml. Suitable work concentration is, 901 strain with 10ug/ml ,801 strain with 12ug/ml and 951 strain with 11ug/ml.

1、抗原的提取:收集新疆不同地区分离得到的利什曼原虫前鞭毛体,经培养,用0.01mol/L pH7.2的磷酸盐缓冲液漂洗,超声粉碎,比色法测定其蛋白质含量,间接ELISA法滴定出抗原的工作稀释度。2、检测:用提取的三株抗原,分别进行间接ELISA法测定黑热病病人血清和疫区健康人血清抗体,并以肺结核病人血清、非疫区健康人血清做对照,三株抗原所用检测方法一致,血清工作稀释度均为1∶100。

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