ACOX2 (GeneName), Peroxisomal acyl-coenzyme A oxidase 2 (ProteinName), ACOX2_HUMAN.
Human 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
Natural and recombinant human 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-hydroxycholestanoic acids.
MGSPVHRVSL | GDTWSRQMHP | DIESERYMQS | FDVERLTNIL | DGGAQNTALR |
RKVESIIHSY | PEFSCKDNYF | MTQNERYKAA | MRRAFHIRLI | ARRLGWLEDG |
RELGYAYRAL | SGDVALNIHR | VFVRALRSLG | SEEQIAKWDP | LCKNIQIIAT |
YAQTELGHGT | YLQGLETEAT | YDAATQEFVI | HSPTLTATKW | WPGDLGRSAT |
HALVQAQLIC | SGARRGMHAF | IVPIRSLQDH | TPLPGIIIGD | IGPKMDFDQT |
DNGFLQLNHV | RVPRENMLSR | FAQVLPDGTY | VKLGTAQSNY | LPMVVVRVEL |
LSGEILPILQ | KACVIAMRYS | VIRRQSRLRP | SDPEAKVLDY | QTQQQKLFPQ |
LAISYAFHFL | AVSLLEFFQH | SYTAILNQDF | SFLPELHALS | TGMKAMMSEF |
CTQGAEMCRR | ACGGHGYSKL | SGLPSLVTKL | SASCTYEGEN | TVLYLQVARF |
LVKSYLQTQM | SPGSTPQRSL | SPSVAYLTAP | DLARCPAQRA | ADFLCPELYT |
TAWAHVAVRL | IKDSVQHLQT | LTQSGADQHE | AWNQTTVIHL | QAAKVHCYYV |
TVKGFTEALE | KLENEPAIQQ | VLKRLCDLHA | IHGILTNSGD | FLHDAFLSGA |
QVDMARTAYL | DLLRLIRKDA | ILLTDAFDFT | DQCLNSALGC | YDGNVYERLF |
QWAQKSPTNT | QENPAYEEYI | RPLLQSWRSK | L
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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