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. 2016 Mar 24;17(4):435. doi: 10.3390/ijms17040435

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© 2016 by the authors; licensee MDPI, Basel, Switzerland.

This article is an open access article distributed under the terms and conditions of the Creative Commons by Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/).

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Determining the RNA interference efficiency of the LV (lentivirus)-EBLN1-shRNA vector in OL. (A) Relative expression of EBLN1 detected by quantitative reverse transcription polymerase chain reaction (qRT-PCR); (B) the electrophoresis of qRT-PCR products. CON (control), uninfected group; NC (negtive control), LV-NC-shRNA group; KD (Knockdown) 1, LV-EBLN1-shRNA1 group; KD2, LV-EBLN1-shRNA2 group; KD3, LV-EBLN1-shRNA3 group. M, DL2000 Maker; B, blank control. * p < 0.001 vs. NC, ** p < 0.05 vs. NC.