نتایج جستجو برای: overlap extension pcr

تعداد نتایج: 366558  

Journal: :iranian journal of biotechnology 2008
malihe nazari jahantigh kamran ghaedi mohamad hossein nasr isfahani somayeh tanhaei farzaneh rabiee

epitope tagging is a method of expressing proteins whereby an epitope for a specific monoclonal antibody is fused to a target protein using recombinant dna techniques. the aim of this study was to sub-clone the peroxisomal protein (pep) cdna into a mammalian expression vector leading to the formation of a  chimeric pep-cdna containing the flag epitope. the flag-pep recombinant cdna was construc...

2013
Letian Chen Fengpin Wang Xiaoyu Wang Yao-Guang Liu

Functional genomics requires vector construction for protein expression and functional characterization of target genes; therefore, a simple, flexible and low-cost molecular manipulation strategy will be highly advantageous for genomics approaches. Here, we describe a Ω-PCR strategy that enables multiple types of sequence modification, including precise insertion, deletion and substitution, in ...

2017
Hui Zhang Chang-Jun Liu Hui Jiang Lu Zhou Wen-Ying Li Ling-Yun Zhu Lei Wu Er Meng Dong-Yi Zhang

Molecular cloning methods based on primer and overlap-extension PCR are widely used due to their simplicity, reliability, low cost and high efficiency. In this article, an efficient mega primer-mediated (MP) cloning strategy for chimaeragenesis and long DNA fragment insertion is presented. MP cloning is a seamless, restriction/ligation-independent method that requires only three steps: (i) the ...

Background: Formation of secondary structure such as DNA hairpins or loops may influence molecular genetics methods and PCR based approaches necessary for genetic engineering, in addition to gene regulation. Materials and Methods: A polymerase chain reaction with splice overlap extension (SOE-PCR) was used to create fully synthetic 1F5 chimeric anti-CD20 heavy- and light-chain genes. The chi...

Background: The immune antigen of Bacillus anthracis is a protein that can attach to the surface receptor of all human cells. At the surface of cancer cells, there is a receptor that activates the uPA (Urokinase plasminogen) that do not exist in normal human cells. Objectives: The aim of this study was changing the location of the attachment of the PA gene by a dir...

Background: The immune antigen of Bacillus anthracis is a protein that can attach to the surface receptor of all human cells. At the surface of cancer cells, there is a receptor that activates the uPA (Urokinase plasminogen) that do not exist in normal human cells. Objectives: The aim of this study was changing the location of the attachment of the PA gene by a dir...

2013
Ran Chai Cuiwei Qiu Dongren Liu Yuancheng Qi Yuqian Gao Jinwen Shen Liyou Qiu

Mushroom β-glucans are potent immunological stimulators in medicine, but their productivities are very low. In this study, we successfully improved its production by promoter engineering in Pleurotus ostreatus. The promoter for β-1,3-glucan synthase gene (GLS) was replaced by the promoter of glyceraldehyde-3-phosphate dehydrogenase gene of Aspergillus nidulans. The homologous recombination frag...

Journal: :research in molecular medicine 0
fatemeh khademi medical biology research center, p. o. box: 6714869914, sorkheh lizheh, kermanshah, iran pantea mohammadi medical biology research center, p. o. box: 6714869914, sorkheh lizheh, kermanshah, iran kheirollah yari medical biology research center, p. o. box: 6714869914, sorkheh lizheh, kermanshah, iran ali mostafaie medical biology research center, p. o. box: 6714869914, sorkheh lizheh, kermanshah, iran

background: formation of secondary structure such as dna hairpins or loops may influence molecular genetics methods and pcr based approaches necessary for genetic engineering, in addition to gene regulation. materials and methods: a polymerase chain reaction with splice overlap extension (soe-pcr) was used to create fully synthetic 1f5 chimeric anti-cd20 heavy- and light-chain genes. the chimer...

Journal: :Applied and environmental microbiology 2015
Man Hwan Oh Je Chul Lee Jungmin Kim Chul Hee Choi Kyudong Han

The traditional markerless gene deletion technique based on overlap extension PCR has been used for generating gene deletions in multidrug-resistant Acinetobacter baumannii. However, the method is time-consuming because it requires restriction digestion of the PCR products in DNA cloning and the construction of new vectors containing a suitable antibiotic resistance cassette for the selection o...

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