Amplification, cloning and expression of Brucella melitensis bp۲۶ gene (OMP۲۸) isolated from Markazi province (Iran) and purification of Bp۲۶ Protein
محل انتشار: مجله آرشیو رازی، دوره: 68، شماره: 2
سال انتشار: 1392
نوع سند: مقاله ژورنالی
زبان: انگلیسی
مشاهده: 92
فایل این مقاله در 6 صفحه با فرمت PDF قابل دریافت می باشد
- صدور گواهی نمایه سازی
- من نویسنده این مقاله هستم
استخراج به نرم افزارهای پژوهشی:
شناسه ملی سند علمی:
JR_ARCHRAZI-68-2_004
تاریخ نمایه سازی: 6 دی 1402
چکیده مقاله:
Brucellosis is a debilitative disease that imposes costs on both economy and society. It is shown that although the vaccine can prevent abortion, it does not provide complete protection against infection. In Iran, Brucella melitensis is a common causative agent for brucellosis and BP۲۶ protein of this bacterium having a good antigenesity and an important vaccine candidate. In this study B. melitensis bp۲۶ gene was cloned first in to PTZ۵۷R/T vector and accessed on the PET۲۸a vector and sequenced. Recombinant vector transformed and expressed in to E. coli BL۲۱ (DE۳) and then recombinant protein was purified with Ni-NTA column of chromatography against His tag. Obtained rOmp۲۸ could be used as a research experimental tool to find its potential as a detection kit and vaccine candidate.
کلیدواژه ها:
نویسندگان
H. Basiri
Department of Microbiology, Islamic Azad University, Arak Branch, Arak, Iran