CERK (K298G, K303G), FLAG-Tag Recombinant

Catalog #
102044
$425 *
Size: 10 µg
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Description

Recombinant human CERK (ceramide kinase), encompassing amino acids 1-537(end). This construct contains a C-terminal FLAG-tag and two mutations of interest (K298G and K303G). This protein was affinity purified.

Synonyms
Acylsphingosine kinase, Lipid kinase 4 (LK4),Ceramide kinase, hCERK, KIAA1646
Product Info
Storage and Usage
Citations
Species
Human
Construct
CERK (K298G, K303G) (1-537(end)-FLAG)
Mutation
K298G, K303G
Host Species/Expression System
Sf9
Purity

≥85%

Format

Aqueous buffer solution.

Formulation

20 mM Tris-HCl, pH 7.4, 104 mM NaCl, 2.2 mM KCl, 20% glycerol, 3 mM DTT, and 80 µg/ml FLAG peptide 

MW
61 kDa
Amino Acids
1-537(end)
Genbank #
NM_022766
UniProt #
Q8TCT0
Tag(s)
C-terminal FLAG-Tag
Background

CERK (ceramide kinase), also known as acylsphingosine kinase, is a protein of the phosphotransferase family involved in ceramide phosphorylation in cell survival and proliferation and support of phagosome formation in leukocytes. It is found mostly in neutrophils, cerebrum granule cells and epithelial lung cells. The human gene includes a RARE (retinoic acid response element)-like transcription motif, which may function to promote expression of CERK in 5H-SY5Y cells when ATRA (all-trans retinoic acid) is present. The phosphorylation of ceramides produces C-1-P (ceramide-1-phosphate), which can help bring cPLA2 (cytosolic phospholipase A2) and CERK together and activate cPLA2. It was found that TPBC (triple-positive breast cancer) and TNBC (triple-negative breast cancer) present CERK dysfunction, and that inhibition of CERK expression or activity could slow down tumor growth. CERK may thus be a promising target in TNBC and TNPC, which currently have very limited therapeutic options.