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CERK converts ceramide to ceramide 1-phosphate (C1P), a sphingolipid metabolite. Additionally we are shipping CERK Kits (11) and CERK Proteins (4) and many more products for this protein.
Showing 10 out of 86 products:
Human Polyclonal CERK Primary Antibody for WB - ABIN391126
Mitsutake, Kim, Inagaki, Kato, Yamashita, Igarashi: Ceramide kinase is a mediator of calcium-dependent degranulation in mast cells. in The Journal of biological chemistry 2004
Show all 6 Pubmed References
Human Polyclonal CERK Primary Antibody for ICC, IF - ABIN251388
Dória, Ribeiro, Wang, Cotrim, Domingues, Williams, Domingues, Helguero: Fatty acid and phospholipid biosynthetic pathways are regulated throughout mammary epithelial cell differentiation and correlate to breast cancer survival. in FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2014
Polyclonal CERK Primary Antibody for WB - ABIN540755
Wijesinghe, Massiello, Subramanian, Szulc, Bielawska, Chalfant: Substrate specificity of human ceramide kinase. in Journal of lipid research 2005
our findings identify a functional role for Cerk in breast cancer recurrence and suggest the clinical utility of agents targeted against this prosurvival pathway.
Data suggest that inhibition of ceramide kinase (CerK) [by specific gene silencing or pharmacological inhibition] drastically reduced cell proliferation in a neuroblastoma (show ARHGEF16 Antibodies) cell line.
TNF-alpha (show TNF Antibodies) exposure of human SH-SY5Y neuroblastoma (show ARHGEF16 Antibodies) caused a profound increase in CERK activity.
Expression of hCERK enhanced ceramide-1-phosphate formation and release of arachidonic acid in Ca(2 (show CA2 Antibodies)+) ionophore-stimulated cells.
We have identified a differential role for ceramide kinase in mast-cell activation
ceramide kinase and its product, C-1-P, have roles in arachidonic acid release and production of eicosanoids
CERK translocates during activation from the cytosol to a lipid raft fraction
Pleckstrin (show PLEK Antibodies) homology domain of CERK is not only indispensable for its activity but also act as a regulator of CERK activity.
sphingoid chain was also required for substrate recognition by CERK
Recombinant CERK was analyzed with regard to dependence on divalent cations, to substrate delivery, specificity, and stereoselectivity. CERK associated with the plasma membrane in CHO (show COL11A1 Antibodies) cells, which is mediated by the N-terminal putative pleckstrin (show PLEK Antibodies) domain.
there are significant differences in eicosanoid levels in ex vivo CERK(-/-) cells compared with wild-type counterparts, but the effect of the genetic ablation of CERK on eicosanoid synthesis and the serum levels of C1P was not apparent in vivo
role of ceramide kinase in obesity and insulin (show INS Antibodies) resistance
Results indicate that C1P produced by CERK has a negative effect on the processing/secretion of TNFalpha (show TNF Antibodies) via modulation of TACE (show ADAM17 Antibodies) activity.
role of CerK on the activation of mast cells
The mechanism of ceramide-mediated inhibition is likely to involve conversion of ceramide to ceramide 1-phosphate by CERK.
LPS (show TLR4 Antibodies) inhibits the transcriptional activity of the Cerk proximal promoter;transcriptional repression of Cerk by LPS (show TLR4 Antibodies) is not a primary consequence of LPS (show TLR4 Antibodies)-induced cell cycle blockade.
Findings suggest that CerK is not necessary for survival at an individual level, but might be involved in higher brain function related to emotion.
CerK is essential to ceramide 1-phosphate formation via phosphorylation of Cer (show CBLN1 Antibodies)
Ceramide kinase is a key regulator of ceramide 1-phosphate, dihydroceramide and ceramide levels, with important implications for neutrophil homeostasis and innate immunity regulation.
CERK converts ceramide to ceramide 1-phosphate (C1P), a sphingolipid metabolite. Both CERK and C1P have been implicated in various cellular processes, including proliferation, apoptosis, phagocytosis, and inflammation (Kim et al., 2006
, Ceramide kinase
, acylsphingosine kinase
, lipid kinase 4
, lipid kinase LK4