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ACOT4 (GeneName), Peroxisomal succinyl-coenzyme A thioesterase (ProteinName), ACOT4_HUMAN.
Product Name:

Human ACOT4/ Peroxisomal succinyl-coenzyme A thioesterase ELISA Kit

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

PTE2B, PTEIB, Acyl-coenzyme A thioesterase 4, Acyl-CoA thioesterase 4, PTE-2b, Peroxisomal acyl coenzyme A thioester hydrolase Ib, Peroxisomal long-chain acyl-CoA thioesterase Ib, PTE-Ib

Detection Method:
ELISA
Specificity:
Natural and recombinant human Peroxisomal succinyl-coenzyme A thioesterase
Sample Type:
Serum, plasma, tissue homogenates, cell culture supernates and other biological fluids
Sample Data:
Research Area:
-
Human ACOT4 ELISA Kit
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Product Datasheets


General Annotation


Sub Unit:
N/A


Function:
Acyl-CoA thioesterases are a group of enzymes that catalyze the hydrolysis of acyl-CoAs to the free fatty acid and coenzyme A (CoASH), providing the potential to regulate intracellular levels of acyl-CoAs, free fatty acids and CoASH (PubMed:16940157). ACOT4 is a peroxisomal succinyl-coenzyme A thioesterase can also hydrolyze glutaryl-CoA and long chain saturated acyl-CoAs (PubMed:16940157).


Subcellular Location:
Peroxisome


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

[1].
"Analysis of the mouse and human acyl-CoA thioesterase (ACOT) gene clusters shows that convergent, functional evolution results in a reduced number of human peroxisomal ACOTs."

[2].
"A revised nomenclature for mammalian acyl-CoA thioesterases/hydrolases."

[3].
"The identification of a succinyl-CoA thioesterase suggests a novel pathway for succinate production in peroxisomes."

[4].
"Complete sequencing and characterization of 21,243 full-length human cDNAs."

[5].
"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."

[6].
"Rare and Coding Region Genetic Variants Associated With Risk of Ischemic Stroke: The NHLBI Exome Sequence Project."

[7].
"An enzyme assisted RP-RPLC approach for in-depth analysis of human liver phosphoproteome."

[8].
"Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium."

[9].
"A proteome-wide perspective on peroxisome targeting signal 1(PTS1)-Pex5p affinities."

[10].
"Toward a confocal subcellular atlas of the human proteome."
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