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Negative regulator of Notch signaling pathway involved furin, maintaining Notch in an immature inactive form, thereby promoting neurogenesis in embryos. Additionally we are shipping CHAC1 Antibodies (47) and and many more products for this protein.
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Chac1 expression is detrimental to arsenite-treated cell survival and TRIB3 (show TRIB3 Proteins) is critical for restraining the pro-death potential of Chac1 during arsenite stress.
Data indicate that Chac1 protein expression was only detected in the presence of MG132, a proteasome inhibitor.
The ChaC family is conversed across all phyla and represents a new pathway for glutathione degradation in living cells, and the first cytosolic pathway for glutathione degradation in mammalian cells.
Human CHAC1 Protein Degrades Glutathione, and mRNA Induction Is Regulated by the Transcription Factors ATF4 (show ATF4 Proteins) and ATF3 (show ATF3 Proteins) and a Bipartite ATF/CRE Regulatory Element.
Botch regulates Notch (show NOTCH1 Proteins) signaling through deglycination and identify a posttranslational modification of Notch (show NOTCH1 Proteins) that plays an important role in neurogenesis.
nisin exerts these effects on HNSCC, in part, through CHAC1, a proapoptotic cation transport regulator, and through a concomitant CHAC1-independent influx of extracellular calcium
High CHAC1 mRNA expression could be an independent indicator for elevated risk of cancer recurrence in breast and ovarian cancer
Negative regulator of Notch signaling pathway involved furin, maintaining Notch in an immature inactive form, thereby promoting neurogenesis in embryos. May also act as a pro-apoptotic component of the unfolded protein response pathway by mediating the pro-apoptotic effects of the ATF4-ATF3-DDIT3/CHOP cascade (By similarity).
cation transport regulator-like protein 1
, ChaC, cation transport regulator-like 1
, ChaC, cation transport regulator homolog 1 (E. coli)
, blocks Notch protein
, cation transport regulator homolog 1
, neuroprotective protein 7