mProX™ Human ESRRB Stable Cell Line
- Product Category:
- Membrane Protein Stable Cell Lines
- Subcategory:
- Nuclear Receptor
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Published Data
Fig.1 Effects of Fgf/Erk signalling inhibition on TS cell transcription factors.
Comparing cells treated with Mek inhibitor PD0325901 ('PD03') for 3, 12, and 24 hours to untreated controls, Western blot analysis revealed the lack of phosphorylated Erk1/2; levels of overall Erk1/2 stayed unaltered. After three hours of PD03 treatment, eSRRB was decreased, and after twelve hours, it was almost nonexistent.
Ref: Latos, Paulina A., et al. "Fgf and Esrrb integrate epigenetic and transcriptional networks that regulate self-renewal of trophoblast stem cells." Nature communications 6.1 (2015): 7776.
Pubmed: 26206133
DOI: 10.1038/ncomms8776
Research Highlights
These findings suggest that Esrrb might function as a bookmarking factor during mitosis, providing a different angle from which to view sequence-specific transcription factors' involvement in the epigenetic regulation of pluripotency, self-renewal, and genome reprogramming.
Festuccia, Nicola, et al. "Mitotic binding of Esrrb marks key regulatory regions of the pluripotency network." Nature cell biology 18.11 (2016): 1139-1148.
Pubmed:
27723719
DOI:
10.1038/ncb3418
Transcription factors (TFs) that cooperate in DNA binding incorporate the cellular environment to facilitate cell specification throughout the developmental process. The pluripotent identity of naive mouse embryonic stem cells can persist indefinitely, as they originate from the early stages of development.
Knudsen, Teresa E., et al. "A bipartite function of ESRRB can integrate signaling over time to balance self-renewal and differentiation." Cell Systems 14.9 (2023): 788-805.
Pubmed:
37633265
DOI:
10.1016/j.cels.2023.07.008