Most mammalian cells contain multiple species of DNA dependent DNA polymerases.

大部分哺乳动物细胞均含有多种依赖DNA的DNA聚合酶.

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The template specificities found with DNA polymerases from human leucocytes is summarized in Table 1.

人的白血病DNA聚合酶的模板特异性简列于表1.

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PCR were using to detect bla ( TEM ), bla ( SHV ) and bla ( CTX - M ) genes.

应用聚合酶链反应(PCR)方法扩增产ESBLs株的bla ( TEM ) 、 bla ( SHV ) 和bla ( CTXM ) 基因.

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The expressions of bcl - x, bax and eNOS were measured by SQ - RT - PCR technique.

采用半定量逆转录聚合酶链反应(SQ-RT-PCR)法检测内皮细胞bcl-x 、 bax以及 eNOS表达.

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Methods: Polymer - ase chain reaction ( PCR ) was used to determine the ACE genotype.

方法: 采用聚合酶链反应 ( PCR ) 方法检测ACE基因型.

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Methods Reverse transcription - polymerase chain reaction ( RT - PCR ), and immunohistochemical method were used.

方法采用反转录 - 聚合酶链反应 ( RT -PCR ) 法和免疫组织化学方法.

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DNA molecule to RNA polymerase binds, initiating the transcription of RNA.

一种rna模板上的dna形成的聚合酶, 尤其在逆转录酶病毒中发现.

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Inhibits platelet aggregation. DNA polymerase inhibitor. Shows antifungal activity.

抑制血小板聚集. DNA聚合酶抑制剂. 显示抗真菌活性.

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Expression of TGF � � 1 was evaluated by RT PCR technique.

逆转录聚合酶链反应(RT?PCR)方法测定肺组织内TGF?β1的表达.

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Conclusion: PCR and ELISA techniques can be used for diagnosis of NTM infection.

结论: 　所用的聚合酶链反应和ELISA有助于诊断非结核分枝杆菌感染.

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Objective : To establish DNA typing for HLA - DR 4 antigen by chain reaction with sequence - specific primers ( PCR - SSP ).

目的: 采用顺序特异引物聚合酶链反应(PCR-SSP ) 建立人类白细胞抗原DR4位点的DNA分型方法.

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BOX - PCR and PBP fingerprint techniques were used to analyze the homology among strains.

并以盒式聚合酶链反应(PCR)和青霉素结合蛋白(PBP)基因指纹等分子生物学方法分析菌株间的亲缘关系.

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In this study, The mRNA expression of VLA - 4 in bone marrow mononuclear cells was measuerd by RT - PCR.

研究采用逆转录-聚合酶链反应(RT -PCR )法检测慢性再障患者治疗前后骨髓单个核细胞VLA -4 的mRNA表达水平.

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Researchers believe that the bird virus polymerase allows for faster replication, and thus more aggressive.

研究人员认为,禽流感病毒聚合酶允许更快的复制, 从而更加积极.

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The fundamental mechanism of transcription is conserved among cellular RNA polymerases, the researchers explained.

转录的基本机制就存在于进化保守的RNA聚合酶中.

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