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TLX1 (HOX11) Immortalization of Embryonic Stem Cell–Derived and Primary Murine Hematopoietic Progenitors
Abstract
The ability to generate genetically engineered cell lines is of great experimental value. They provide a renewable source of material that may be suitable for biochemical analyses, chromatin immunoprecipitation assays, structure‐function studies, gene function assignment, and transcription factor target gene identification. This unit describes protocols for TLX1 (HOX11)‐mediated immortalization of murine hematopoietic progenitors derived from in vitro differentiated murine embryonic stem cells, or from primary mouse fetal liver or bone marrow. A wide variety of hematopoietic cell types have been immortalized using these procedures including erythroid, megakaryocytic, monocytic, myelocytic, and multipotential cell types. These lines are typically cytokine dependent for their survival and growth. Curr. Protoc. Stem Cell Biol. 7:1F.7.1‐1F.7.19. © 2008 by John Wiley & Sons, Inc.
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“The overexpression of the HOX11 and TLX1 genes can lead the hematopoietic precursor cells, mouse fetal liver, or bone marrow towards immortalization.”
From Cell Immortality: In Vitro Effective Techniques to Achieve and Investigate Its Applications and Challenges (2024) · cites this paper as [88]
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Cited by
Chalak, M., Hesaraki, M., Mirbahari, S. N., Yeganeh, M., Abdi, S., Rajabi, S., & Hemmatzadeh, F. (2024) · Life · doi:10.3390/life14030417 · Cited by 66
Liu, Z., Ciocea, A., & Devireddy, L. (2014) · Molecular and Cellular Biology · doi:10.1128/mcb.00231-14 · Cited by 41
Metadata
- Authors
- Hawley, R. G., Hawley, T. S., & Cantor, A. B.
- Affiliations
- The George Washington University Medical Center Washington D.C.
- Flow Cytometry Core Facility, The George Washington University Medical Center Washington D.C.
- Department of Pediatric Hematology‐Oncology, Childrens's Hospital Boston Boston Massachusetts
- Venue
- Current Protocols in Stem Cell Biology
- Publisher
- Wiley
- Published
- 2008-12
- Volume
- 7
- Issue
- 1
- ISSN
- 1941-7322
- 1938-8969
- PMC
- PMC2633409
- Cited by
- 4
- References
- 2
- Language
- en
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