ABHD12 (GeneName), Lysophosphatidylserine lipase ABHD12 (ProteinName), ABD12_BOVIN.
Bovine ABHD12/ Lysophosphatidylserine lipase ABHD12 ELISA Kit
Abhydrolase domain-containing protein 12, 2-arachidonoylglycerol hydrolase ABHD12, Monoacylglycerol lipase ABHD12, Oxidized phosphatidylserine lipase ABHD12
Natural and recombinant bovine Lysophosphatidylserine lipase ABHD12
Serum, plasma, tissue homogenates, cell culture supernates and other biological fluids
Lysophosphatidylserine (LPS) lipase that mediates the hydrolysis of lysophosphatidylserine, a class of signaling lipids that regulates immunological and neurological processes (By similarity). Represents a major lysophosphatidylserine lipase in the brain, thereby playing a key role in the central nervous system (By similarity). Also able to hydrolyze oxidized phosphatidylserine; oxidized phosphatidylserine is produced in response to severe inflammatory stress and constitutes a proapoptotic 'eat me' signal. Also has monoacylglycerol (MAG) lipase activity: hydrolyzes 2-arachidonoylglycerol (2-AG), thereby acting as a regulator of endocannabinoid signaling pathways. Has a strong preference for very-long-chain lipid substrates; substrate specificity is likely due to improved catalysis and not improved substrate binding (By similarity).
Endoplasmic reticulum membrane Single-pass membrane protein
MRKRTEPVAL | EHERRTASGS | PSAGPAAAAL | DADCRLKQNL | CLAGPGPAEP |
RCAADAGMKR | ALGRRKGLC | FRLRKILFFV | LGLYVAIPFL | IKLCPGIQAK |
LIFLNFVRVP | YFIDLKRPQD | Q GLNHTCNY | YLQPEEDVTI | GVWHTVPTVW |
WKNAQGKDQM | WYEDALSSSH | PIILYLHGNA | GT RGGDHRV | ELYKVLSSLG |
YHVVTFDYRG | WGDSVGTPSE | RGMTYDALHV | FDWIKVRSGD | NPV YIWGHS |
LGTGVATNLV | RRLCERETPP | DALILESPFT | NIREEAKSHP | FSVIYRYFPG |
FDWF FLDPI | TSSGIQFAND | ENVKHISCSL | LILHAEDDPV | VPFQLGRKLY |
NIAAPSRSFR | DFKVQ FIPF | HSDLGYRHKY | IYKSPELPRI | LREFLGKSEP |
This product has not yet been referenced specifically in any publications.
"Biochemical and pharmacological characterization of human α/β-hydrolase domain containing 6 (ABHD6) and 12 (ABHD12)."
"Biochemical and pharmacological characterization of the human lymphocyte antigen B-associated transcript 5 (BAT5/ABHD16A)."
"Two novel mutations in ABHD12: expansion of the mutation spectrum in PHARC and assessment of their functional effects."
"Targeted next-generation sequencing identifies a homozygous nonsense mutation in ABHD12, the gene underlying PHARC, in a family clinically diagnosed with Usher syndrome type 3."
"Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma."
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