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Expression, purification and antibody preparation of recombinat SARS-CoV X5 protein / 药学学报
Acta Pharmaceutica Sinica ; (12): 1157-1160, 2008.
Article in Chinese | WPRIM | ID: wpr-232625
ABSTRACT
X5 protein is one of the putative unknown proteins of SARS-CoV. The recombinant protein has been successfully expressed in E. coli in the form of insoluble inclusion body. The inclusion body was dissolved in high concentration of urea. Affinity Chromatography was preformed to purify the denatured protein, and then the product was refolded in a series of gradient solutions of urea. The purified protein was obtained with the purity of > 95% and the yield of 93.3 mg x L(-1). Polyclonal antibody of this protein was obtained, and Western blotting assay indicated that the X5 protein has the strong property of antigen. Sixty-eight percent of the recombinant protein sequence was confirmed by LC-ESI-MS/MS analysis.
Subject(s)
Full text: Available Index: WPRIM (Western Pacific) Main subject: Viral Proteins / Recombinant Proteins / Molecular Sequence Data / Gene Expression Regulation, Viral / Inclusion Bodies / Chemistry / Amino Acid Sequence / Severe acute respiratory syndrome-related coronavirus / Allergy and Immunology / Escherichia coli Limits: Animals Language: Chinese Journal: Acta Pharmaceutica Sinica Year: 2008 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Viral Proteins / Recombinant Proteins / Molecular Sequence Data / Gene Expression Regulation, Viral / Inclusion Bodies / Chemistry / Amino Acid Sequence / Severe acute respiratory syndrome-related coronavirus / Allergy and Immunology / Escherichia coli Limits: Animals Language: Chinese Journal: Acta Pharmaceutica Sinica Year: 2008 Type: Article