Abstract
Delivery of conventional antisense oligonucleotides or small interfering RNA (siRNA) molecules into hematolymphoid cells for targeted gene silencing has been proven to be difficult. Here, we describe a simple protocol to knockdown specific gene(s) in malignant hematolymphoid cells using “GapmeR.” This protocol could be applicable to a wide range of cell-types and thus solves an important problem for researchers working with cell lines or primary cells derived from patients with hematolymphoid malignancies.
Original language | English |
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Title of host publication | Methods in Molecular Biology |
Publisher | Humana Press Inc. |
Pages | 209-219 |
Number of pages | 11 |
DOIs | |
Publication status | Published - 2020 |
Externally published | Yes |
Publication series
Name | Methods in Molecular Biology |
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Volume | 2176 |
ISSN (Print) | 1064-3745 |
ISSN (Electronic) | 1940-6029 |
Bibliographical note
Publisher Copyright:© Springer Science+Business Media, LLC, part of Springer Nature 2020.
ASJC Scopus Subject Areas
- Molecular Biology
- Genetics
Keywords
- GapmeR
- Gene knockdown
- HuT78
- Lymphoma cells
- RNAi
- STAT3