mProX™ Human TRPC7 Stable Cell Line
- Product Category:
- Membrane Protein Stable Cell Lines
- Subcategory:
- Ion Channel Cell Lines
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Published Data
Fig.1 Ultraviolet B (UVB)-induced pathology decreased in TRPC7 knockdown cells.
Senescent and nonsenescent cells in different TRPC knockdown keratinocytes were counted after a 24-hour UVB exposure, and the ratio between the two was computed. Senescence-associated β-galactosidase (SA-β-gal) staining was used to identify cell senescence.
Ref: Hsu, Wen-Li, et al. "Nociceptive transient receptor potential canonical 7 (TRPC7) mediates aging-associated tumorigenesis induced by ultraviolet B." Aging Cell 19.1 (2020): e13075.
Pubmed: 31755176
DOI: 10.1111/acel.13075
Research Highlights
TRP canonical 7 (TRPC7) is a nociceptive mechanoreceptor; mutations in the p53 gene family particularly cause TRPC7 channels to trigger the onset of UVB-induced skin aging and tumor growth.
Hsu, Wen-Li, et al. "Nociceptive transient receptor potential canonical 7 (TRPC7) mediates aging-associated tumorigenesis induced by ultraviolet B." Aging Cell 19.1 (2020): e13075.
Pubmed:
31755176
DOI:
10.1111/acel.13075
TRPC7 uses two different methods to control how automated mESC-CMs are. In addition to positively regulating the membrane clock through its impact on NCX activity, TRPC7 also positively regulates the intracellular Ca2+ clock by controlling the activities of both RyR2 and SERCA.
Liu, Xianji, et al. "TRPC7 regulates the electrophysiological functions of embryonic stem cell-derived cardiomyocytes." Stem Cell Research & Therapy 12.1 (2021): 1-18.
Pubmed:
33941260
DOI:
10.1186/s13287-021-02308-7