Volume 5, Issue 4 (Winter 2013 2014)                   2014, 5(4): 831-836 | Back to browse issues page


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samaei N, Naderi M, khajeh H, moradipour N, gholipour N, *,Zarghami Moghaddam P. Optimization of PCR product of GC rich astrocyte elevated gene 1 promoter. North Khorasan University of Medical Sciences 2014; 5 (4) :831-836
URL: http://journal.nkums.ac.ir/article-1-141-en.html
Abstract:   (4840 Views)

Abstract Background and Objectives: Most housekeeping genes, tumor-suppressor genes, and approx 40% of tissue specific genes contain G+C sequences in their promoter region that are very difficult to amplify. AEG-1 plays a significant role in invasion, metastasis, angiogenesis and chemoresistance, apoptosis, angiogenesis and aging Material and Methods:In this study, we proposed an improved polymerase chain reaction (PCR) method to be used for successful amplification of the Astrocyte elevated gene -1gene promoter region that contains >70% G+C content in a sequence of 495 bp and some transcription initiation sites in hepatocellularcarcinoma patient. Results: The results showed that using of DMSO co-amplification touchdown PCR and pfu enzyme can inhibit the formation of secondary structure in DNA Sequences and increase the PCR product. Conclusion: Therefore, this method can be recommended to amplify other GC-rich genomic templates.

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Type of Study: Orginal Research | Subject: Basic Sciences
Received: 2015/01/1 | Accepted: 2015/01/1 | Published: 2015/01/1

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