• FluTrackers.com Inc. does not provide medical advice. Information on this web site is collected from various internet resources, and the FluTrackers board of directors makes no warranty to the safety, efficacy, correctness or completeness of the information posted on this site by any author or poster. The information collated here is for instructional and/or discussion purposes only and is NOT intended to diagnose or treat any disease, illness, or other medical condition. Every individual reader or poster should seek advice from their personal physician/healthcare practitioner before considering or using any interventions that are discussed on this website. By continuing to access this website you agree to consult your personal physican before using any interventions posted on this website, and you agree to hold harmless FluTrackers.com Inc., the board of directors, the members, and all authors and posters for any effects from use of any medication, supplement, vitamin or other substance, device, intervention, etc. mentioned in posts on this website, or other internet venues referenced in posts on this website.
  • We are not asking for any donations. Do not donate to any entity who says they are raising funds for us.

Construction and expression of eukaryotic expression vector of NS1 protein of influenza A (H1N1)

tetano

Editor, Senior Moderator
Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2011 Mar;27(3):287-289.
[Construction and expression of eukaryotic expression vector of NS1 protein of influenza A (H1N1).]

[Article in Chinese]

Zhang WS, Bian Q, Wen T, Chi Y, Li Y, Jiao YJ.

Key Laboratory of Enteric Pathogenic Microbiology, Ministry of Health, Institute of Pathogenic Microbiology, Jiangsu Provincial Center for Disease Prevention and Control, Nanjing 210009, China.
Abstract

AIM: To insert the full-length NS1 gene of influenza A (H1N1) into an eukaryotic expression vector PXJ40-HA, and to evaluate the expression of NS1 gene in transfected 293T cells.

METHODS: The NS1 gene of influenza A (H1N1) was amplified by RT-PCR and cloned into pMD18-T vector to construct a plasmid, named pMD18-T-NS1.The pMD18-T-NS1 and the PXJ40-HA were both digested using the same restrict enzymes and ligated, yielding the recombinant eukaryotic expression vector PXJ40-HA-NS1. The expression of the NS1 gene in transfected 293T cells was tested by Western blot.

RESULTS: The recombinant eukaryotic expression vector PXJ40-HA-NS1 was successfully constructed. The NS1 protein was observed to be expressed in 293T cells.

CONCLUSION: The full-length NS1 gene is obtained and its recombinant eukaryotic expression plasmid is successfully constructed. This study is of help to further understanding the biological function of NS1 protein and the mechanism of diseases induced by influenza A virus.

PMID: 21419049 [PubMed - as supplied by publisher]

http://www.ncbi.nlm.nih.gov/pubmed/21419049
 
Back
Top