mProX™ Human CSNK1E Stable Cell Line
- Product Category:
- Membrane Protein Stable Cell Lines
- Subcategory:
- Kinase Cell Lines
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Published Data
Fig.1 Loss of CSNK1E function abrogates Wnt/β-catenin signaling.
A β-catenin expression construct, pRL-SV40, the specified shRNA construct, and the β-catenin-responsive pTOPFLASH reporter constructs were cotransfected into 293T cells. Immunoblot study of MCF7 cells 72 hours after transduction with shRNA against CSNK1E, showing levels of nuclear (right) and cytoplasmic (left) β-catenin.
Ref: Kim, So Young, et al. "CK1ε is required for breast cancers dependent on β-catenin activity." PloS one 5.2 (2010): e8979.
Pubmed: 20126544
DOI: 10.1371/journal.pone.0008979
Research Highlights
Finding circadian genes that are differently expressed in KIRC and evaluating their significance in the development of KIRC were the objectives of this investigation. There were 553 differentially expressed rhythm genes (DERGs) in KIRC; of them, 253 were down-regulated and 300 were up-regulated.
Li, Shujing, et al. "Effects and prognostic values of circadian genes CSNK1E/GNA11/KLF9/THRAP3 in kidney renal clear cell carcinoma via a comprehensive analysis." Bioengineering 9.7 (2022): 306.
Pubmed:
35877357
DOI:
10.3390/bioengineering9070306
In this Korean population, CSNK1E SNP rs2075984 appeared to be crucial in the onset of bipolar disorder. The phase preference as determined by the CS does not appear to be related to this connection. Larger sample sizes and additional SNPs are required for further research on CSNK1E.
Lee, Kyu Young, et al. "Genetic association study of CSNK1E gene in bipolar disorder and circadian characteristics." Nordic Journal of Psychiatry 72.8 (2018): 599-604.
Pubmed:
30445897
DOI:
10.1080/08039488.2018.1509125