مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

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Information Journal Paper

Title

RT-PCR CLONING AND EXPRESSION OF COMPLEMENTARY DNA FOR HUMAN TUMOR NECROSIS FACTOR ALPHA

Pages

  58-62

Abstract

 U-937, a monocytic cell line was induced with Phorbol Myristate Acetate (PMA) for human tumor necrosis factor alpha (hTNF-α) production. An optimized RT-PCR was employed for construction of hTNF- α complementary DNA (cDNA). The resulted fragment was verified by restriction digestion mapping with PvuII. The verified fragment was cloned in pUC18 plasmid and transformants were pelletted onto LB agar medium containing ampicillin, X-gal and IPTG. The resulting white colonies were verified by PCR and cultured in LB medium containing ampicillin and IPTG. The biological activity and the quantity of hTNF- α expression was assessed by an ELISA method using a monoclonal anti hTNF- α antibody together with a bioassay utilizing L-929 line as sensitive cells.  

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    Cite

    APA: Copy

    SEPEHRIZADEH, Z., KHORAMIZADEH, MOHAMMAD REZA, & TABATABAEI YAZDI, S.M.. (2003). RT-PCR CLONING AND EXPRESSION OF COMPLEMENTARY DNA FOR HUMAN TUMOR NECROSIS FACTOR ALPHA. DARU JOURNAL OF PHARMACEUTICAL SCIENCE, 11(2), 58-62. SID. https://sid.ir/paper/275192/en

    Vancouver: Copy

    SEPEHRIZADEH Z., KHORAMIZADEH MOHAMMAD REZA, TABATABAEI YAZDI S.M.. RT-PCR CLONING AND EXPRESSION OF COMPLEMENTARY DNA FOR HUMAN TUMOR NECROSIS FACTOR ALPHA. DARU JOURNAL OF PHARMACEUTICAL SCIENCE[Internet]. 2003;11(2):58-62. Available from: https://sid.ir/paper/275192/en

    IEEE: Copy

    Z. SEPEHRIZADEH, MOHAMMAD REZA KHORAMIZADEH, and S.M. TABATABAEI YAZDI, “RT-PCR CLONING AND EXPRESSION OF COMPLEMENTARY DNA FOR HUMAN TUMOR NECROSIS FACTOR ALPHA,” DARU JOURNAL OF PHARMACEUTICAL SCIENCE, vol. 11, no. 2, pp. 58–62, 2003, [Online]. Available: https://sid.ir/paper/275192/en

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