hNaDC1 gene 5 flanking region of transcriptional regulatory sequences and identification of series of vectors.docVIP
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hNaDC1 gene 5 flanking region of transcriptional regulatory sequences and identification of series of vectors
PAGE \* MERGEFORMAT 11
hNaDC1 gene 5 ‘flanking region of transcriptional regulatory sequences and identification of series of vectors
Authors: Zhang Jiankai, Yang Ju-rong, LI Xue-Peng, HE Ya-ni
[Abstract] Objective To construct hNaDC1 gene 5 ‘flanking region of transcription regulating sequence series of firefly luciferase reporter gene expression vector. Methods PCR amplification hNaDC1 gene 5 ‘flanking transcriptional regulatory region fragments of different lengths: hNaDC1A (-2 232 / 136,2 368 bp), hNaDC1B (-1 640 / 136,1 776 bp), hNaDC1C (-1 084 / 136 , 1 221 bp), hNaDC1D (-253 / 136,389 bp), hNaDC1E (-2 232/-12, 2 244 bp), with pGL3 Basic for vector hNaDC1 gene 5 ‘flanking sequence of series of deletion plasmids. Recombinant enzyme by specific restriction enzyme digestion, and send sample sequencing. The results successfully constructed hNaDC1 gene 5 ‘flanking region transcriptional regulatory elements firefly luciferase reporter gene expression vector 5: pGL3 hNaDC1A ~ E. Conclusions for further research NaDC1 gene 5 ‘flanking region of the distribution of transcriptional regulatory elements and transcription regulatory elements and transcription factor interactions provide the basic experimental conditions.
[Keywords:] hNaDC1 gene regulation of gene expression vector
Abstract: Objective To construct the firefly luciferase report gene vectors for 5 ‘flanking regulated elements of hNaDC1 gene. MethodsThe DNA fragments hNaDC1A ~ E (-2 232 / 136) in 5’flanking region of hNaDC1 gene were amplified from the nephridial tissue by using PCR. The PCR products were directionally subcloned into pGL3 Basic vector. The recombined clones were identified by agarose gel electrophoresis after restriction endonuclease digesting and DNA sequencing. Results 5 expression vectors (pGL3 NaDC1A ~ E) for 5 ‘flanking regulated elements of hNaDC1 gene had been constructed. ConclusionThese expression vectors offer the basic experimental conditions for studying the
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