• Objective:To explore a simple and reliable technique to keep positive DNA controls.

    目的探索能获得阳性DNA对照简便可靠方法

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  • We applied the sister chromatid exchange (SCE) technique to pregnant women with antibodies against cytomegalovirus (CMV) positive, to detect the lesion and repair of DNA in the lymphocytes.

    采用孕妇外周血淋巴细胞姐妹染色单体交换SCE技术检测巨细胞病毒CMV抗体阳性孕妇淋巴细胞DNA损伤修复

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  • Meanwhile, biochemical reaction, coagglutination test, metabolism-inhibition test, polymerase chain reaction (PCR), and DNA sequence assay were employed to identify those positive cultures.

    阳性培养物用生化反应、协同凝集试验代谢抑制试验、聚合酶链反应DNA测序加以鉴定

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  • Methods HBV genotypes were detected by polymerase chain reaction (PCR) and restriction fragment length polymorphism analysis (RFLP) in 136 HBV DNA positive patients who were born in Shanghai.

    方法采用聚合酶链反应-限制性片段长度多态性分析(PCR - RFLP)检测136例HBVDNA阳性的上海籍HBV感染者的基因型。

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  • Objective: To identify positive clones from DNA recombinants rapidly.

    目的DNA重组体中快速鉴定出阳性克隆

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  • Plasmid DNA and chromosomal DNA of the strain CEOI all obtained positive dot-blot to plasmid probe and chromosomal probe correspondingly.

    dna染色体dna分别与质粒探针和染色体探针杂交出现典型阳性杂交斑。

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  • Objective to observe the therapeutic effect of autologous cytokine-induced killer cells (CIK) on HBV DNA positive patients with liver cirrhosis.

    目的观察体细胞因子诱导杀伤细胞(CIK细胞)治疗HBVDNA阳性肝硬化患者近期疗效。

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  • All the 6 genotypes (9 strains) of measles virus showed DNA positive strand, it means this RT-PCR method is sensitive for measles viruses.

    结果96种基因型麻疹病毒RT PCR均呈现阳性条带,说明本研究采用的RT PCR方法敏感

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  • The positive control cell line DNA was mixed in different proportions with the DNA extracted from reactive lymphoid tissue to test the sensitivity of the touch-down PCR.

    阳性细胞系DNA模板反应增生性淋巴组织DNA不同比例混合扩增检测降落式PCR灵敏度

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  • Objective To study the effect of HBV-DNA positive serum on phenotypic transformation of renal tubular epithelial cells.

    目的研究HBV - DNA阳性血清小管上皮细胞表型转化作用

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  • Objective To acknowledge the existence and replication of TTV DNA in peripheral blood mononuclear cells(PBMC) of patients with serum TTV DNA positive.

    目的了解TTV阳性肝炎患者外周血单个核细胞PBMC)TTVDNA存在复制情况。

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  • Sandwich ELISA, dot blotting and DNA sequencing methods were used for the identification of positive clones.

    通过硝酸纤维膜斑点印迹进行阳性克隆鉴定

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  • Results: 39 out of 41 HCMV-DNA positive samples were identified positive and all of the 232 HCMV-DNA negative samples were negative by this method.

    结果41例证实为HCMV - DNA阳性标本中该产前诊断方法检测39例方法对232例HCMV - DNA阴性标本诊断为阴性。

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  • Methods To introduce DNA encoding the wild- type and mutant channel into immortalized tyrosine hydroxylase- positive CNS- derived neurons, CAD cells.

    方法一类酪氨酸脱氢酶阳性神经细胞(一种中枢神经源细胞),又称CAD细胞,引入DNA编码野生突变型离子通道

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  • Specific antibody was screened by 3 rounds of panning of phage antibody library with the fusion protein. The antigen binding activity and DNA sequences of positive clones were determined and analyzed.

    融合蛋白为固相抗原噬菌体抗体进行3,并对所获阳性克隆进行抗原结合活性测定DNA序列测定。

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  • Provides complete reagents including positive and negative control slides for convenient detection of DNA fragmentation in tissue sections and fixed cell preps. Results can be analyzed by microscopy.

    提供完整组份包括阳性阴性对照组织切片便于检测组织切片固定细胞中的片段dna结果通过显微镜分析

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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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  • But in control group, positive rate was only less than 5%, and we could only see a single normal DNA strip.

    对照细胞呈现阳性染色者每视野超过5%,DNA凝胶电泳只见正常基因组dna带。

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  • Result in the PCR amplification sensitivity testing revealed that 0.021 egg DNA template would be enough to amplify this specific positive band.

    PCR扩增敏感性检测结果表明,0.021个虫卵dna模板即可扩增特异性阳性条带

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  • TB-DNA was detected in 8 of 41 malignant tumor tissues (19 5%), moreover, the incidence locations of TB-DNA positive malignant tumors were mostly similar to that of tuberculosis.

    结果41例恶性肿瘤组织检出TB - dna阳性患者8例,占19.5 %,TB - dna阳性患者肿瘤发病部位基本结核病好发部位一致。

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  • The appearance of double bands in several inbred lines by some primers was probably caused by electrophic difference between positive and negative DNA chains.

    在试验中某些亲本自交系出现双带,分析认为可能由于正负链电泳行为差异造成的。

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  • Objective To study the clinical application of DNA chip for common Gram-positive bacteria identification and drug resistance detection.

    目的利用基因芯片技术进行常见革兰阳性细菌细菌鉴定耐药性检测

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  • HPV DNA testing already has a poor positive predictive value, especially in younger girls, they point out, and the absolute number of true positive tests would decrease substantially in this scenario.

    他们指出HPVDNA检验阳性预测值已经不高特别是年轻的女性这种情况下,阳性检验绝对数目将会显著降低

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  • DNA sequence assays showed that 5 of the 6 positive clones displayed the same peptide sequences.

    DNA测序结果显示所得到6个噬菌体阳性克隆中,有5个阳性克隆递呈相同的氨基酸序列。

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  • Aim To explore the effect lamivudine (LMV) on the liver function of patients with HBV DNA positive pulmonary tuberculosis.

    目的探讨拉米呋啶(LMV)HBVDNA阳性肺结核患者肝功能干预作用

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  • That implies that these regions are so important for the organism that their DNA sequences are maintained by positive selection.

    意味着这些区域对于机体如此重要以至于它们DNA序列通过主动选择来保持

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  • And there was a positive correlation between the area and DNA content.

    并且面积DNA含量之间具有明显的正相关关系。

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  • Results For 18 nasopharyngeal carcinoma patients, positive rates of EB virus DNA in plasma and leucocytes were 61%(11/18);

    结果18鼻咽癌患者外周血血浆白细胞检测EB病毒DNA阳性率相同,均为61%(11/18);

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  • The positive cells were selected by G418, genome DNA of the positive cells was extracted and sequenced.

    g 418筛选阳性细胞提取阳性细胞基因组d NA测序

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  • Results: Reliable detection of DNA methylation of TLX3 and FOXE3 segregated ALL from those clear of disease with minimal false-negative and false-positive results.

    结果:在最小限度阴性假阳性结果中,TLX3和FOXE3DNA甲基化检测可有效鉴别ALL

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