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Acox2 (GeneName), Peroxisomal acyl-coenzyme A oxidase 2 (ProteinName), ACOX2_RAT.
Product Name:

Rat Acox2/ Peroxisomal acyl-coenzyme A oxidase 2 ELISA Kit

Cat.#:
-
Brand:
EIAab®
Regulatory Status:
Alternative:

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

Detection Method:
ELISA
Specificity:
Natural and recombinant rat Peroxisomal acyl-coenzyme A oxidase 2
Sample Type:
Serum, plasma, tissue homogenates, cell culture supernates and other biological fluids
Sample Data:
Research Area:
Cardiovascular
Rat Acox2 ELISA Kit
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Product Datasheets


General Annotation


Sub Unit:
N/A


Function:
Oxidizes the CoA esters of the bile acid intermediates di- and tri-hydroxycoprostanic acids.


Subcellular Location:
Peroxisome


This product has not yet been referenced specifically in any publications.

[1].
"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."

[2].
"ACOX2 deficiency: An inborn error of bile acid synthesis identified in an adolescent with persistent hypertransaminasemia."

[3].
"Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score."

[4].
"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."

[5].
"Assignment of the human peroxisomal branched-chain acyl-CoA oxidase gene to chromosome 3p21.1-p14.2 by rodent/human somatic cell hybridization."

[6].
"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."

[7].
"Separate peroxisomal oxidases for fatty acyl-CoAs and trihydroxycoprostanoyl-CoA in human liver."

[8].
"Architecture of the human interactome defines protein communities and disease networks."

[9].
"ACOX2 deficiency: A disorder of bile acid synthesis with transaminase elevation, liver fibrosis, ataxia, and cognitive impairment."

[10].
"SR protein kinases promote splicing of nonconsensus introns."
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