• Bluetongue Virus (BTV), Bovine anti -, Negative Control.

    病原蓝舌病毒(BTV),阴性对照

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  • Results: The spots were clear, negative control without interference by TLC.

    结果:薄层色谱斑点清晰阴性对照干扰

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  • Results the spots in the TLC were clear and identified without the interference of negative control.

    结果薄层图谱斑点清晰阴性对照干扰

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  • Results: The spots in TLC were clear and easy to be identified, negative control without interference.

    结果薄层色谱斑点清晰易于辨别阴性对照干扰。

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  • Methods:Rats were divided into blank control group, negative control group, model group and icariin treatment group.

    方法分为空白对照组阴性对照组、模型、淫藿苷治疗组;

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  • From 31 days all rats were sensitized and chanllenged to induce asthma with OVA but in negative control group using N.

    生后日龄第31天时,所有大鼠OVA制作哮喘模型,阴性对照组N

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  • Virus without anti-Smad was served as negative control, and that without adenovirus vector was served as blank control.

    空载病毒作为阴性对照组,以病毒载体作为空白对照组。

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  • ResultsCompared with negative control group, lung congestion and lung edema of ligustrazine low-dose group were mitigated.

    结果阴性对照组相比,川芎嗪低剂量组织病理显示肺淤血肺水肿明显减轻

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  • The rate of PCE micronucleus induced by different dosages showed no significant difference from the negative control group.

    剂量诱导PCE微核细胞率阴性对照组比较显著性差异

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  • Compared with negative control group, the doubling time of both positive control group and experimental groups was prolonged.

    阴性对照组比较阳性对照组实验组细胞群体倍增时间增加。

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  • Each 10 guinea pigs were immunized with fresh HAM homogenate, albumen solution (positive control) and PBS (negative control).

    新鲜羊膜组、新鲜蛋清组(阳性对照)PBS液组(阴性对照),10豚鼠

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  • Flow cytometric analysis of MCF-7 cells, using MUC1 (VU4H5) Mouse mAb (blue) compared to a nonspecifc negative control antibody (red).

    使用MUC1VU4H5单抗(蓝色MCF-7细胞进行流式分析对照使用阴性对照抗体红色)。

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  • Methods The sera of schistosomiasis cattle, negative control cattle and fascioliasis cattle were detected with DDIA and compared with COPT.

    以确定的最适条件血吸虫病阴性对照肝片形吸虫病牛的血清进行检测并和环卵沉淀试验(COPT)检测结果进行比较

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  • Methods:To test it with sodium tetraphenylborate method increasing negative control and the control of reagent and cancel carboration ash steps.

    方法:采用四苯硼检测增加阴性对照管及试剂对照管,取消炭化化的步骤

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  • Objective: To measure the samples of antler powder, Runing Granules containing antler powder and negative control sample (without antler powder).

    目的鹿角鹿角粉的乳冲剂、乳宁冲剂阴性样品进行检测

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  • Flow cytometric analysis of C2C12 cells using HSP27 Antibody (Rodent Preferred) (blue) compared to a nonspecific negative control antibody (red).

    使用HSP27抗体啮齿类偏好)()和非特异阴性对照抗体(红),C2C12细胞进行流式细胞仪分析

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  • Results The degree of airsacculitis and fibrosis in model group are obviously higher than the negative control group by pathological observation.

    结果肺组织病理形态学观察发现模型小鼠肺泡纤维化程度明显高于阴性对照组

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  • On the negative control sections, almost all cells were semitransparent, and without coloration , and the background of slices almost had no color.

    用作阴性对照样品切片上,镜下几乎所有细胞半透明着色深染细胞,切片背景基本着色

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  • Nonphosphorylated MKK3/MKK6 Control Cell Extracts: Total cell extracts from NIH/3T3 cells, prepared without treatment, serve as a negative control.

    非磷酸化的MKK3/MKK6细胞提取物未经处理NIH/3T3细胞提取物,作为阴性对照

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  • Compared with the negative control group, the Zn, fe, ca, Mg concentrations of the low, moderate and high DHPO groups were not significantly different.

    剂量大鼠肾脏中锌含量阴性对照组相比差异无统计学意义。

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  • In other hand, in the groups with low energy level but added NSP enzymes, the nutrients digestibility were higher than the negative control significant.

    同时,对照组相比,处于同等低能水平条件下,添加NSP可使能量及其他养分利用率显著提高

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  • Figure 4 a: Amplification curves of positive and negative controls in specific test. We can see that negative control did not amplify and was a straight line.

    4A特异性实验中的阳性阴性对照扩增曲线,阴性对照图中显示条直线,扩增。

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  • Also provides complete components including positive and negative control cells for convenient detection of DNA fragmentation in cultured cells by flow cytometry.

    该试剂盒提供完整组份包括阳性阴性对照细胞便于采用流式细胞术检测培养细胞中的片段化dna

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  • Immortalized human embryonic kidney cell line HEK293 and the human embryonic lung fibroblasts HELF were used as positive control and negative control, respectively.

    同时以端粒酶阳性的永生化纤维细胞HEK293作为阳性对照,以端粒酶阴性的人胚成纤维细胞HELF作为阴性对照。

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  • To verify testing conditions, a negative control is performed using the chosen diluent in place of the test preparation. There must be no growth of micro-organisms.

    检测试验条件是否符合要求,取试验稀释液代替供试品做阴性对照试验,阴性对照试验微生物生长

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  • The animal model of tail scales of mouse was taken. To be divided into three groups: the normal saline negative control group, the low dose group, the high dose group.

    通过小鼠鳞片实验模型,设生理盐水剂量组,观察各组对小鼠尾部鳞片颗粒层形成的影响

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  • Methods Rats were randomly divided into negative control (no treatment) group, positive control (1% sulfadiazine silver cream) group and test (CSP) group, respectively.

    方法将大鼠随机分为阴性对照组(空白)、阳性对照组(1%磺胺嘧啶乳膏组)实验组(CSP组)。

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  • The result showed that VEGF ASODN had obviously inhibitive effect on expression of VEGF in U937 cell, as compared with scrambled sequence and negative control (P<0.05).

    结果显示VEGFASODNU937细胞VEGF的表达有明显的抑制作用,错义序列组空白对照组相比有显著差异(P<0 .0 5 ) ;

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  • The phagocytosis rate results showed that compared with negative control, both venom injection and parasitization could suppress the phagocytosis rate of pupal hemocytes.

    吞噬测定结果表明对照相比,寄生毒液处理显著降低蛹血细胞吞噬能力。

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  • Comparison of tie results of the high dosage groups of amiprophos and of MMS with that of the negative control (P<0.01) showed marked significance as well a dose response.

    剂量MMS空白对照组比较,有非常显著意义P<0.01),且有剂量效应关系。

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