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摘要翻译
人α-防御素HNP-2基因真核表达载体的构建摘要目的:构建人α-防御素HNP-2真核表达载体。方法:利用PCR技术从质粒pET-28a(+)扩增人α-防御素HNP-2全长...
人α-防御素HNP-2基因真核表达载体的构建
摘 要
目的:构建人α-防御素HNP-2真核表达载体。方法:利用PCR技术从质粒pET-28a(+)扩增人α-防御素HNP-2全长基因,HindⅢ和EcoRⅠ分别酶切目的基因和载体pcDNA3.1(+),分别回收小片段和大片段,利用T4 DNA酶连接构建重组表达载体pcDNA3.1(+) /HNP-2,转化大肠杆菌DH5α,经快速PCR筛选和酶切、测序鉴定载体成功构建。 结果:经双酶切法酶切鉴定证实真核表达载体构建准确无误。结论:成功构建真核表达载体pcDNA3.1(+)/HNP-2,为进一步研究打下了基础 展开
摘 要
目的:构建人α-防御素HNP-2真核表达载体。方法:利用PCR技术从质粒pET-28a(+)扩增人α-防御素HNP-2全长基因,HindⅢ和EcoRⅠ分别酶切目的基因和载体pcDNA3.1(+),分别回收小片段和大片段,利用T4 DNA酶连接构建重组表达载体pcDNA3.1(+) /HNP-2,转化大肠杆菌DH5α,经快速PCR筛选和酶切、测序鉴定载体成功构建。 结果:经双酶切法酶切鉴定证实真核表达载体构建准确无误。结论:成功构建真核表达载体pcDNA3.1(+)/HNP-2,为进一步研究打下了基础 展开
2个回答
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The construction of human's α-defensinHNP-2 gene eukaryotic expression vector.
Summary
Objective:Build human α-defensinHNP-2 eukaryotic expression vector.
Method:Amplify human's α-defensinHNP-2full-length gene, from plasmid pET-28a(+) by using PCR ,Hind Ⅲ andEcoR Ⅰenzyme cut target gene and vector pcDNA3.1(+),Separately recoveringsmallfragments andthe large fragment,UsingT4 DNA ligase to construct recombinant expression vector pcDNA3.1(+)/HNP-2 and escherichia coli DH5α,
Identify carrier successfully build by rapiding PCR screening and restriction enzyme digestion, sequencing.
Consequent :
Confirmed the eukaryotic expression vector construct accurate by double digestion method
digestion appraisal
Conclusion:
Constructed the eukaryotic expression vector pcDNA3.1(+)/HNP-2 successful.
Summary
Objective:Build human α-defensinHNP-2 eukaryotic expression vector.
Method:Amplify human's α-defensinHNP-2full-length gene, from plasmid pET-28a(+) by using PCR ,Hind Ⅲ andEcoR Ⅰenzyme cut target gene and vector pcDNA3.1(+),Separately recoveringsmallfragments andthe large fragment,UsingT4 DNA ligase to construct recombinant expression vector pcDNA3.1(+)/HNP-2 and escherichia coli DH5α,
Identify carrier successfully build by rapiding PCR screening and restriction enzyme digestion, sequencing.
Consequent :
Confirmed the eukaryotic expression vector construct accurate by double digestion method
digestion appraisal
Conclusion:
Constructed the eukaryotic expression vector pcDNA3.1(+)/HNP-2 successful.
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