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ELISA相关的网络例句

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与 ELISA 相关的网络例句 [注:此内容来源于网络,仅供参考]

At 10 weeks, smooth muscle bundles were observed and there were no significant difference between the two groups of the number of neogenesis capillary and positive VEGFR2 expression cells. To understand the release of exogenous growth factors from small intestinal submuscosa in bladder regeneration, the release of vascular endothelial growth factor and basic fibroblast growth factor from SIS in vitro were evaluated by ELISA and MTT method.

尽管文献报道制备的小肠粘膜下层中含有少量细胞生长因子,但尚不明确其在动物体内是否仍具有生物活性,为了解小肠粘膜下层在膀胱组织修复中外源性生长因子VEGF和bFGF释放,我们用ELISA法和MTT法体外测量冻干SIS在PBS孵育液中VEGF和bFGF的含量及对上皮细胞的增殖作用;用猪小肠粘膜下层行大鼠膀胱部分修复。

At pre-operation, post-operation 6 h, 3 d and 7 d detect the leave of plasm prethrombotic state molecular marker tissue factor, tissue factor pass inhibitory, thrombus precursor protein, plasminogen activator inhibitory-1(PAI-1), P-Selectin, Thrombin-Antithrombin complexes, D-dimer with ELISA, transmission immunity nephelometer. Results Malignant tumor patients, the levels of plasma TF, TpP, D-D in 6 h and 3 d of post-operation rose to peak value.

分别于术前、术后6 h3、d和7 d用ELISA、透射免疫比浊法检测其血浆血栓前状态分子标志物D-二聚体(D-dimer, D-D)、血栓前体蛋白(thrombus precursor protein, TpP)、凝血酶抗凝血酶复合物(thrombin-antithrombin complexes, TAT)、组织因子(tissue factor, TF)、P选择素(P-Selectin, P-S)、组织因子途径抑制物(tissue factor pass inhibitory, TFPI)、纤溶酶原激活物抑制物1(plasminogen activator inhibitory-1, PAI-1)的水平。

Finally, the change of neuroglia which expressing GFAP and CD11b was counted by immunohistochemistry and the expression of IFN-γ/IL-10 in serum was measured by ELISA.

用免疫组化法测定腰髓中表达GFAP和CD11b的阳性细胞数;用ELISA法测定血清IFN-γ和IL-10水平。

Methods ①In situ hybridization was applied to observe the changes ofhypothalamic CRHmRNA positive cells after PX and melatonin supplementation;②Immunohistochemistry was used to observe the changes of CRH positive cellsin hypothalamus and CRH staining in median eminence of neurohypophysis after PXand melatonin supplementation;③ELISA was applied to detect the changes of CRHconcentration in serum after PX and melatonin supplementation.

①运用CRHmRNA 原位杂交的方法来观察松果体摘除及补充外源性褪黑素后下丘脑室旁核CRHmRNA 阳性细胞的变化;②应用免疫组织化学染色的方法观察松果体摘除及补充外源性褪黑素后下丘脑室旁核CRH 阳性细胞和神经垂体正中隆起CRH 阳性染色的变化;③运用ELISA 法检测松果体摘除及补充褪黑素后血清CRH 浓度的变化。

Results ①Compared to sham group, ISH and IHC of rat hypothalamic CRHshow positive cells numbers increase, positive areas enlarge and average gray scaledecreases, which reveals the expression of hypothalamic CRH neurons enhances afterPX;②The enhancement of ISH and IHC of hypothalamic CRH in PX rats aftermelatonin supplementation dose-dependently recovers, but it can't return to be normaleither in high dose group or in low dose group and either at 4th week or at 8th week;③IHC of CRH in median eminence of neurohypophysis shows positive areas enlargeand average gray scale decreases, which reveals the releasing of CRH fromhypothalamic CRH neurons increases;④ELISA of CRH in serum shows thedifferences of CRH concentrations among all groups are not significant, which indicates PX and melatonin supplementation have no significant effect on CRH levels.

结果: ①松果体摘除后大鼠下丘脑室旁核CRH 原位杂交和免疫组化的结果与假手术对照组相比均显示阳性细胞数增多、阳性面积增加、平均灰度降低,提示松果体摘除后下丘脑CRH 神经元的表达增强;②松果体摘除大鼠补充褪黑素后,下丘脑CRH 原位杂交和免疫组化染色增强呈剂量依赖性恢复,不过不论是低剂量组还是高剂量组,也不论是术后4 周还是术后8周,均不能恢复至正常;③松果体摘除后神经垂体正中隆起CRH 免疫组化结果显示阳性面积增加、平均灰度降低,提示下丘脑CRH 神经元释放CRH 增加;④ELISA 法检测血清CRH结果示各组血清CRH 浓度差异没有显著性,表明松果体摘除及补充褪黑素对血清CRH 水平没有显著影响。

Results ①Compared to sham group, ISH and IHC of rat hypothalamic CRHshow positive cells numbers increase, positive areas enlarge and average gray scaledecreases, which reveals the expression of hypothalamic CRH neurons enhances afterPX;②The enhancement of ISH and IHC of hypothalamic CRH in PX rats aftermelatonin supplementation dose-dependently recovers, but it can't return to be normaleither in high dose group or in low dose group and either at 4th week or at 8th week;③IHC of CRH in median eminence of neurohypophysis shows positive areas enlargeand average gray scale decreases, which reveals the releasing of CRH fromhypothalamic CRH neurons increases;④ELISA of CRH in serum shows thedifferences of CRH concentrations among all groups are not significant, whichindicates PX and melatonin supplementation have no significant effect on CRH levels.

结果: ①松果体摘除后大鼠下丘脑室旁核CRH 原位杂交和免疫组化的结果与假手术对照组相比均显示阳性细胞数增多、阳性面积增加、平均灰度降低,提示松果体摘除后下丘脑CRH 神经元的表达增强;②松果体摘除大鼠补充褪黑素后,下丘脑CRH 原位杂交和免疫组化染色增强呈剂量依赖性恢复,不过不论是低剂量组还是高剂量组,也不论是术后4 周还是术后8周,均不能恢复至正常;③松果体摘除后神经垂体正中隆起CRH 免疫组化结果显示阳性面积增加、平均灰度降低,提示下丘脑CRH 神经元释放CRH 增加;④ELISA 法检测血清CRH结果示各组血清CRH 浓度差异没有显著性,表明松果体摘除及补充褪黑素对血清CRH 水平没有显著影响。

Before the first immune and 1 week after strengthened immune, take blood and measure AsAb with ELISA method, measure the immune integral of IgG and IgA in uterus tunica intima with SABC method; meanwhile, compare the pregnant rats and average nidation points in all groups.

在首次免疫前、各次加强免疫后1周取血ELISA法测定AsAb,SABC法检测子宫内膜IgG、IgA免疫积分,同时比较各组大鼠受孕数及孕鼠平均着床点数。

Methods Volunteers of medical staff responsible for respiratory infection from 7 hospitals in Hubei province were enrolled. A self-report standard questionnaire was used to assess the general state of well-being and the frequency of airway infection during recent two years. Sera from the medical staffs and from the age-matched healthy subjects of nonmedical occupation were tested by ELISA for SCPIgG.

方法随机抽样湖北地区7所医院中经常接诊呼吸道感染患者自愿参加的健康医务人员,以问卷方式询问他们近2年发生呼吸道感染的机会;以ELISA法检测血清CP特异性免疫球蛋白G抗体,并与健康体检非医务成人SCPIgG抗体资料进行比较。

For recombinant nucleoprotein and spike protein,we developed an ELISA to test these two antibodies.

以ELISA法分别检测抗-SARS-CoVIgM和IgG抗体、SARS-CoVN蛋白和S蛋白IgG抗体。

Oncidium and Cymbidium with symptom of viral disease affect with ORSV or CyMV by ELISA.

利用ELISA技术在感病文心兰和大花惠兰样品可以检测到建兰花叶病毒和齿兰环斑病毒。

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