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RIOK1 includes two alternatively spliced transcript variants, which encode different isoforms.
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we demonstrate that RIOK1 promotes lung colonization in vivo and that RIOK1 is overexpressed in different subtypes of human lung- and breast cancer.
methionine adenosyltransferase II alpha (MAT2A (show MAT2A ELISA Kits)), and the arginine methyltransferase, PRMT5, as vulnerable enzymes in cells with MTAP (show MTAP ELISA Kits) deletion.
The RIO kinase fold generates a versatile ATPase enzyme, which in the case of Rio1 is activated following the Rio2 step to regulate one of the final 40S maturation events, at which time the 60S subunit is recruited for final quality control check.
These results imply that, in glioblastoma cells, constitutive Akt (show AKT1 ELISA Kits) signaling drives RIO kinase overexpression, which creates a feedforward loop that promotes and maintains oncogenic Akt (show AKT1 ELISA Kits) activity through stimulation of mTor (show FRAP1 ELISA Kits) signaling.
RioK1, a new interactor of protein arginine methyltransferase 5 (PRMT5), competes with pICln for binding and modulates PRMT5 complex composit (show NCL ELISA Kits)ion and substrate specificity.
Describes a function for human RIOK1 as a component of the protein arginine methyltransferase 5 complex, conferring specificity for nucleolin (show NCL ELISA Kits) as a methylation substrate.
This gene includes two alternatively spliced transcript variants, which encode different isoforms. The function of this gene has not been determined.
serine/threonine-protein kinase RIO1