Sentence examples for drive vector from inspiring English sources

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We sought to target endogenous p53 wt to both drive vector expression and inhibit tumor proliferation by including the p19Arf cDNA in the pCLPG retrovirus, a vector that contains a p53-responsive promoter used to control expression of the transgene.

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The propagator matrices, the blocked drive vectors, the specifically assigned response vectors, and the impedances of the dynamic systems at the stems of the junctions all assume new forms.

In some cases, a double promoter system has also been used to drive vector-based siRNA expression, where two promoters are in tandem or in opposite directions (11- 13).

With the insect transformation technology to create transgenic insects bearing genes that can be used for their control, transposons gained much attention to be potential gene drive vectors to spread transgenes among pest populations to achieve genetic control [ 14].

The purpose of this article is to document the details of in-flight calibration of the Swarm magnetometer package, including an empirical determination and removal of the Sun-driven vector disturbance field (delta vec {B}_mathrm {Sun}), based on a mitigation approach proposed by Vincent Lesur (Lesur et al. 2015).

TNF-α, TLR-4, and GADPH clones for use as standards were prepared by PCR from cDNA derived from PM and cloned into p-Drive vector (Qiagen, S.p.A., Milano, Italy).

Briefly, for each gene tested, reference plasmids containing the target sequence were produced (by cloning into p-drive Vector) and the amount of plasmid measured using a Nano-drop Spectrophotometer ND-10000, Labtech International).

Any endo-hydrogenase driven, vector H+ translocation, an energy-requiring process, would be necessarily slow by comparison with exo-hydrogenase activity, uncoupled from H+ translocation, and thus relatively fast.

When the pCLPG vector was employed for transfer of the p53 cDNA, a positive feedback regulatory mechanism was established that both drove vector expression and also blocked tumor cell proliferation [ 22].

In order to investigate the cellular localization of the putative SAMD9 protein, the open reading frame of the SAMD9 gene was cloned, an N-terminal EGFP tag was added and subcloned into a CMV driven vector pLP-EGFP-C1 (Clontech, USA).

To validate our reporter gene assay and rule out any technical differences in luciferase activity in NALM6 vs. CCRF-CEM cells, we assayed a CMV promoter-luciferase driven vector (pCMV-luc) and found no significant differences in both cell lines (data not shown).

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