Copy number variation-associated lncRNAs may contribute to the etiologies of congenital heart disease.
Lu Y, Fang Q, Qi M, Li X, Zhang X, Lin Y, Xiang Y, Fu Q, Wang B
Commun Biol. 2023 Feb 17;6(1):189. doi: 10.1038/s42003-023-04565-z.
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Plasmids from Article
| ID | Plasmid | Purpose |
|---|---|---|
| 197902 | pLVX-shRNA2-zsGreen-PGK-puro_HSALNG0104472-163 | For the stable knockdown experiments using shRNA, a complementary sequence (HSALNG0104472-163) targeting the HSALNG0104472 transcript was inserted. |
| 197989 | PCDH-CMV-MCS-EF1a-gfp-T2A-puro_HSALNT0217290 | For the overexpression experiments, full length of the transcript (HSALNT0217290) for HSALNG0104472 was inserted. |
| 197991 | pLVX-shRNA2-zsGreen-PGK-puro_scramble shRNA | For the stable knockdown experiments using shRNA, scramble sequence was inserted as the control. |