1、

Using Alkaline Lysis Method for Recombine Plasmid DNA Extraction and PCR Verification

碱裂解法提取重组质粒DNA及PCR验证

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2、

Detection of abundance of Pseudomonas in environmental samples by real-time quantitative PCR

实时荧光定量PCR法检测环境假单胞菌属细菌丰度

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3、

The GRK 2/ 3 and the mRNA of CRH were measured by Western blot and reverse transcriptional polymerase chain reaction ( RT-PCR) respectively.

通过western blot实验研究室旁核GRK2/3的蛋白表达,逆转录多聚酶链反应(RT-PCR)技术研究室旁核CRH的转录活性。

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4、

A real-time quantitative PCR method of testing the plasma FLV load

鼠艾滋病模型血浆病毒载量荧光定量PCR检测方法的建立

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5、

Differential diagnosis of H5 、 H9 subtype of avian influenza virus by multiplex RT-PCR

禽流感病毒H5、H9亚型的多重RT-PCR鉴别诊断

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6、

Multiplex RT-PCR for Detection of Different Subtype ( H5 and H9) of Avian Influenza Virus

禽流感病毒H5和H9亚型多重RT-PCR快速检测方法的建立

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7、

Determination of the DAZ Gene in Human Sperm by Quantitative PCR

定量PCR法测定人精子中DAZ基因的相对含量

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8、

Use of fluorescent PCR in diagnosis of male infertility related DAZ Gene

荧光PCR在男性不育相关DAZ基因检测中的运用

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9、

RT-PCR method was established to identify the virus by type 1 and novel DHV primers respectively.

利用Ⅰ型和新型鸭肝炎病毒鉴别引物对提取的病毒RNA进行了RT-PCR扩增。

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10、

The mutant gene can be identified by PCR and testing enzyme activity of CPY. The mutant strain inheritance and ferment stability is well.

通过对目的基因的扩增和羧肽酶Y酶活检测验证基因敲除情况,并通过传代抗性试验与传代发酵稳定性实验验证突变株遗传稳定性良好。

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11、

Study on allele-specific diagnostic PCR of the traditional Chinese medicines of the deers

鹿类中药材的位点特异性PCR鉴定研究

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12、

Bacteria in colony were identified with gram stain and PCR method.

细菌通过革兰染色和PCR法鉴定。

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13、

The results showed that expression of Notch 1 receptor was detected in cord blood derived CD34+ cells by RT PCR.

结果表明,RT PCR方法检测到脐带血CD34+细胞表达Notch1受体。

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14、

Methods: RT-PCR was used to examine the expression of Notch-1 and its ligands on cord blood cells.

方法:RT PCR用于检测Notch1及其配体在脐带血细胞上的表达情况。

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15、

Development and Initial Application of nested RT-PCR Method for Japanese Encephalitis virus

日本脑炎病毒套式RT-PCR方法的建立与初步应用

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16、

Detection of Epstein-Barr virus DNA by two temperature PCR cycles

双温聚合酶链反应检测EB病毒

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17、

Amplification of the DNA Polymerase I Gene of Treponema Pallidum by PCR and its Application in Diagnosis of Primary Syphilis

PCR扩增梅毒螺旋体poIA基因及其在一期梅毒诊断中的应用

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18、

Methods: According to specific sequence of Treponema pallidum gene ( tpp47 gene), a pair of specific primers were designed and PCR assay was developed.

方法:根据梅毒螺旋体47ku膜蛋白基因序列,自行设计筛选一对特异寡核苷酸引物,建立梅毒螺旋体的PCR。

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19、

Objective: To establish PCR assay for rapid detection of Treponema pallidum.

目的:建立聚合酶链反应(PCR)用于快速检测梅毒螺旋体。

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20、

51 clinical samples were detected by dark-field microscopy and a double-primer PCR, the positive rates were 15.7% and 19.6%, respectively.

检测了51例临床标本,梅毒螺旋体暗视野显微镜检查阳性检出率为15.7%,双引物PCR阳性检出率为19.6%;

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