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کاربرد نوع شرط:
- جایگاه : پژوهشی
- مجله: Journal of Pharmaceutical and Health Sciences (JPHS)
- نوع مقاله: Journal Article
- کلمات کلیدی: Escherichia coli,urinary tract infection,Cloning,cellular immune system
- چکیده:
- چکیده انگلیسی: Urinary tract infections are one of the most common infectious diseases that lead to significant health problems in the world. Urinary tract infections are referred to any infection in any part of the renal system. Uropathogenic Escherichia coli, Proteus mirabilis, and Klebsiella are main organisms that are involved in these infections.
After identifying same protective and conserved virulence sequences in these microorganisms with similarity upper than 80%, sequences of synthetic gene was provided by bioinformatics techniques and ordered from Thermo Fisher Scientific Company. PCR amplification of this gene was performed by specific primers designed for this purpose. Construction of gene was performed by overlap PCR. The synthetic gene was cloned into pET28a vector. Our gene was amplified in E. coli Top10 tested.
To confirm cloning, three methods including colony PCR, digestion and sequencing were used. First, two techniques were performed using horizontal electrophoresis, and also the synthetic gene showed significant homology with the sequence (99% Identified) in sequencing. Sequencing of this gene showed that fusion was constructed correctly. Determination of biochemical properties such as 3D structure, Ramachandran and comparison of Non-redundant Set of PDB structure was done by bioinformatic software and had exact and expectable results.
A large part of the health system in the world is occupied by a urinary tract infection and governments spend a huge amount of money for the treatment and recovery of patients with these infections. On the other hands, antibiotic resistance in the not-far future will be a disaster for medical societies. This is the most important reason for the emergence of vaccine production against urinary tract infections.- انتشار مقاله: 30-05-1396
- نویسندگان: Jamil Kheirvari Khezerloo,Zohreh Haghri,Mana Oloomi,Mohammad Reza Asadi Karam,Mehri Habibi
- مشاهده
- جایگاه : پژوهشی
- مجله: Asian Pacific Journal of Cancer Prevention
- نوع مقاله: Journal Article
- کلمات کلیدی: Breast cancer,Prognosis,RT-PCR,CEA
- چکیده:
- چکیده انگلیسی: Background: Carcinoembryonic antigen (CEA) detection was evaluated in breast cancer (BC). The statistical correlation between the CEA mRNA and clinico-pathological features in the peripheral blood (PB) and tissue samples of BC was assessed. Materials and Methods: RT-PCR (Reverse transcription-polymerase chain reaction) analysis was applied to study the expression of CEA in PB of 30 healthy females and 30 patients with operable BC before receiving any therapy, as well as in the tissue of 30 BC patients. Results: CEA was observed in a number of normal subjects, but there was a significant difference between the patients and controls. The detected CEA mRNA from tissue samples were the same as PB of patients and a correlation was observed between the CEA mRNA in PB and tissue samples (Pearson chi-square = 8.62, P=0.003). In the PB, CEA mRNA was significantly different in HER-2 (-)/HR (+) compare with HER-2(+)/HR (-) tumor group (p=0.026). Finally, CEA in serum was also significantly different in HER-2(-)/HR (+) compared with HER-2(+)/HR (+) and HER-2(+)/HR (-) subtypes (p=0.008 and p=0.043, respectively). Conclusion: CEA mRNA evaluation is diagnostically valuable as a breast cancer marker. Additionally, CEA can significantly improve the sensitivity of diagnosis.
- انتشار مقاله: 29-01-1398
- نویسندگان: Neda Moazzezy,Saeid Bouzari,Mana Oloomi
- مشاهده