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ACSF2 Antibody [F15E3]

Cat.No.: F4977

    Application: Reactivity:
    • F4977-wb
      Lane 1: Jurkat

    Usage Information

    Dilution
    1:2000-1:10000
    1:8000
    Application
    WB, FCM, ELISA
    Reactivity
    Human
    Source
    Rabbit Monoclonal Antibody
    Storage Buffer
    PBS, pH 7.2+50% Glycerol+0.05% BSA+0.01% NaN3
    Storage (from the date of receipt)
    -20°C (avoid freeze-thaw cycles), 2 years
    Predicted MW Observed MW
    68 kDa 51-71 kDa
    *Why do the predicted and actual molecular weights differ?
    The following reasons may explain differences between the predicted and actual protein molecular weight.

    Datasheet & SDS

    Biological Description

    Specificity
    ACSF2 Antibody [F15E3] detects endogenous levels of total ACSF2 protein.
    Clone
    F15E3
    Synonym(s)
    ACSF2; Medium-chain acyl-CoA ligase ACSF2, mitochondrial; UNQ493/PRO1009
    Background
    ACSF2 (acyl-CoA synthetase family member 2) is a mitochondrial matrix enzyme that catalyzes the activation of medium-chain fatty acids into acyl-CoA thioesters, a crucial step for β-oxidation and maintaining lipid homeostasis. It possesses a canonical AMP-binding superfamily architecture, including an N-terminal mitochondrial targeting sequence that is cleaved upon import, an ATP-grasp domain responsible for Mg-ATP binding, an A10-like subdomain forming the substrate-binding cleft for fatty acid interaction, and a C-terminal dimerization domain that enables obligatory homodimerization. ACSF2 operates via a two-step ping-pong mechanism, where ATP thioesterification forms an acyl-AMP intermediate followed by nucleophilic displacement by the CoA thiol to generate acyl-CoA and AMP, with a marked specificity for medium-chain fatty acids. This enzyme supports mitochondrial β-oxidation by enabling CPT1-independent import of medium-chain fatty acids, bypassing carnitine shuttle limitations. Deficiency of ACSF2 leads to combined malonic and methylmalonic aciduria (CMAMMA), resulting in the accumulation of dicarboxylic acids due to impaired fatty acid catabolism and deficits in protein lipoylation, which are essential for mitochondrial enzyme complex stability. Somatic overexpression of ACSF2 is associated with non-alcoholic fatty liver disease and hepatocellular carcinoma through dysregulated hepatic VLDL secretion and increased lipid droplet accumulation.
    References
    • https://pubmed.ncbi.nlm.nih.gov/36160020/
    • https://www.biorxiv.org/content/10.1101/2022.03.28.486105v1.abstract

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