catalog number :
MBS711296
products full name :
Rabbit anti-human acyl-Coenzyme A oxidase 2, branched chain polyclonal Antibody
products short name :
acyl-Coenzyme A oxidase 2, branched chain
products name syn :
acyl-Coenzyme A oxidase 2; branched chain; ACOX2; BCOX; BRCACOX; BRCOX; THCCox
other names :
Acyl-Coenzyme A oxidase 2, branched chain; Peroxisomal acyl-coenzyme A oxidase 2; peroxisomal acyl-coenzyme A oxidase 2; THCA-CoA oxidase; trihydroxycoprostanoyl-CoA oxidase; acyl-Coenzyme A oxidase 2, branched chain; peroxisomal branched chain acyl-CoA oxidase; 3-alpha,7-alpha,12-alpha-trihydroxy-5-beta-cholestanoyl-CoA oxidase; 3-alpha,7-alpha,12-alpha-trihydroxy-5-beta-cholestanoyl-CoA 24-hydroxylase; acyl-CoA oxidase 2, branched chain; 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; THCCox
other gene names :
ACOX2; ACOX2; BCOX; BRCOX; THCCox; BRCACOX; THCA-CoA oxidase; THCCox
uniprot entry name :
ACOX2_HUMAN
reactivity :
Human, Mouse, Rat
purity :
Antigen Affinity Purified
tested application :
ELISA (EIA), Immunohistochemistry (IHC), Immunofluorescence (IF)
other info1 :
Immunogen: Human ACOX2
other info2 :
Storage Buffer: PBS with 0.02% Sodium Azide, 50% Glycerol, pH 7.3. -20 degree C, Avoid freeze / thaw cycles.
ncbi acc num :
AAH47700.1
ncbi mol weight :
76,827 Da
ncbi pathways :
Beta-oxidation Of Pristanoyl-CoA Pathway 106138!!Bile Acid And Bile Salt Metabolism Pathway 106144!!Bile Acid Biosynthesis, Cholesterol = Cholate/chenodeoxycholate Pathway 413432!!Bile Acid Biosynthesis, Cholesterol = Cholate/chenodeoxycholate Pathway 468297!!Metabolic Pathways 132956!!Metabolism Pathway 477135!!Metabolism Of Lipids And Lipoproteins Pathway 160976!!PPAR Signaling Pathway 83042!!PPAR Signaling Pathway 450!!Peroxisomal Lipid Metabolism Pathway 106136
ncbi summary :
The product of this gene belongs to the acyl-CoA oxidase family. It encodes the branched-chain acyl-CoA oxidase which is involved in the degradation of long branched fatty acids and bile acid intermediates in peroxisomes. Deficiency of this enzyme results in the accumulation of branched fatty acids and bile acid intermediates, and may lead to Zellweger syndrome, severe mental retardation, and death in children. [provided by RefSeq, Mar 2009]