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1Vatche and Tamar Manoukian Division of Digestive Diseases, Department of Medicine,University of California, Los Angeles, 2Vatche and Tamar Manoukian Division of Digestive Diseases, Integrated Molecular Technologies (IMT) Core, Department of Medicine,University of California, Los Angeles, 3Division of Hematology and Oncology, Department of Medicine,University of California, Los Angeles
Chapters
- 00:04Title
- 00:40Vector Design and Generation
- 01:52Virus Generation
- 04:24Particle Count using p24 Enzyme-linked Immunosorbent Assay Kit
- 07:07dCas9 and gRNA Transduction, Selection, and Clone Creation
- 10:18Results: Using CRISPR Technology to Overexpress Multiple Splice Variants of a lncRNA
- 12:08Conclusion
Las técnicas tradicionales basados en cDNA sobreexpresión tienen una aplicabilidad limitada para la sobreexpresión de larga noncoding RNAs debido a sus múltiples formas de empalme con la funcionalidad potencial. Esta revisión informa un protocolo usando tecnología de CRISPR para sobreexpresar múltiples variantes de empalme de un ARN largo cubierta.
