mProX™ Human CACNA1C Stable Cell Line
- Product Category:
- Membrane Protein Stable Cell Lines
- Subcategory:
- Ion Channel Cell Lines
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Published Data
Fig.1 CCAT is Translated from an Independent Transcript Driven by an Exonic Promoter.
mRNA isolated from Neuro2A cells producing Cav1.2-Gal4 channel constructs with or without the CMV promoter was subjected to Northern blot analysis. The mRNA from untransfected cells is in the first lane.
Ref: Gomez-Ospina, Natalia, et al. "A promoter in the coding region of the calcium channel gene CACNA1C generates the transcription factor CCAT." PloS one 8.4 (2013): e60526.
Pubmed: 23613729
DOI: 10.1371/journal.pone.0060526
Research Highlights
Numerous large-scale genome-wide association studies have repeatedly demonstrated that the risk of psychiatric diseases is increased by genetic variation in CACNA1C. The voltage-gated calcium channel Cav1.2 subunit, which is encoded by CACNA1C, has been functionally linked to a wide range of neuropsychiatric disorders.
Moon, Anna L., et al. "CACNA1C: association with psychiatric disorders, behavior, and neurogenesis." Schizophrenia bulletin 44.5 (2018): 958-965.
Pubmed:
29982775
DOI:
10.1093/schbul/sby096
Numerous mental illnesses have been linked to calcium channel subunits, such as CACNA1C. In particular, genome wide association studies (GWAS) have consistently found a high correlation between schizophrenia and bipolar disorder and the single nucleotide polymorphism (SNP) rs1006737 in CACNA1C's intron 3.
Eckart, Nicole, et al. "Functional characterization of schizophrenia-associated variation in CACNA1C." PLoS One 11.6 (2016): e0157086.
Pubmed:
27276213
DOI:
10.1371/journal.pone.0157086