Acox2 (GeneName), Peroxisomal acyl-coenzyme A oxidase 2 (ProteinName), ACOX2_RAT.
Rat Acox2/ Peroxisomal acyl-coenzyme A oxidase 2 ELISA Kit
3-alpha, 7-alpha, 12-alpha-trihydroxy-5-beta-cholestanoyl-CoA 24-hydroxylase, 3-alpha, 7-alpha, 12-alpha-trihydroxy-5-beta-cholestanoyl-CoA oxidase, Trihydroxycoprostanoyl-CoA oxidase, THCA-CoA oxidase, Thcox
Natural and recombinant rat Peroxisomal acyl-coenzyme A oxidase 2
Serum, plasma, tissue homogenates, cell culture supernates and other biological fluids
Oxidizes the CoA esters of the bile acid intermediates di- and tri-hydroxycoprostanic acids.
MGSPMHRVSL | GDHWSWQVHP | DIDSERHSPS | FSVERLTNIL | DGGLPNTVLR |
RKVESIIQSD | PVFNLKKLYF | MTREELYEDA | IQKRFHLEKL | AWSLGWSEDG |
PERIYANRVL | DGNVNLSLHG | VAMNAIRSLG | SDEQIAKWGQ | LCKNFQIITT |
YAQTELGHGT | YLQGLETEAT | YDEARQELVI | HSPTMTSTKW | WPGDLGWSVT |
HAVVLAQLTC | LGVRHGMHAF | IVPIRSLEDH | TPLPGITVGD | IGPKMGLEHI |
DNGFLQLNHV | RVPRENMLSR | FAEVLPDGTY | QRLGTPQSNY | LGMLVTRVQL |
LCKGILPSLQ | KACIIATRYS | VIRHQSRLRP | SDPEAKILEY | QTQQQKLLPQ |
LAVSYAFHFT | ATSLSEFFHS | SYSAILKRDF | SLLPELHALS | TGMKATFADF |
CAQGAEICRR | ACGGHGYSKL | SGLPTLVARA | TASCTYEGEN | TVLYLQVARF |
LMKSYLQAQA | SPGATPQKPL | PQSVMYIATQ | RPARCSAQTA | ADFRCPDVYT |
TAWAYVSTRL | IRDAAHRTQT | LMKSGVDQHD | AWNQTTVIHL | QAAKAHCYFI |
TVKNFKEAVE | KLDKEPEIQR | VLQRLCDLYA | LHGVLTNSGD | FLHDGFLSGA |
QVDMAREAFL | DLLPLIRKDA | ILLTDAFDFS | DHCLNSALGC | YDGHVYERLF |
EWAQKYPANT | QENPAYKKYI | RPLMLGWRHK | M
This product has not yet been referenced specifically in any publications.
"Molecular characterization of the human peroxisomal branched-chain acyl-CoA oxidase: cDNA cloning, chromosomal assignment, tissue distribution, and evidence for the absence of the protein in Zellweger syndrome."
"ACOX2 deficiency: An inborn error of bile acid synthesis identified in an adolescent with persistent hypertransaminasemia."
"Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score."
"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."
"Assignment of the human peroxisomal branched-chain acyl-CoA oxidase gene to chromosome 3p21.1-p14.2 by rodent/human somatic cell hybridization."
"The CoA esters of 2-methyl-branched chain fatty acids and of the bile acid intermediates di- and trihydroxycoprostanic acids are oxidized by one single peroxisomal branched chain acyl-CoA oxidase in human liver and kidney."
"Separate peroxisomal oxidases for fatty acyl-CoAs and trihydroxycoprostanoyl-CoA in human liver."
"Architecture of the human interactome defines protein communities and disease networks."
"ACOX2 deficiency: A disorder of bile acid synthesis with transaminase elevation, liver fibrosis, ataxia, and cognitive impairment."
"SR protein kinases promote splicing of nonconsensus introns."
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