Fatty Acid Transport Protein 4 (FATP4)

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SLC27A4; ACSVL4; Long-Chain Fatty Acid Transport Protein 4; Solute Carrier Family 27 Member 4,Fatty Acid Transporter

Fatty Acid Transport Protein 4 (FATP4)
SLC27A4 encodes a member of a family of fatty acid transport proteins, which are involved in translocation of long-chain fatty acids cross the plasma membrane. This protein is expressed at high levels on the apical side of mature enterocytes in the small intestine, and appears to be the principal fatty acid transporter in enterocytes. Clinical studies suggest this gene as a candidate gene for the insulin resistance syndrome. Furthermore, overexpression of FATP4 in 293 cells facilitated uptake of long chain fatty acids with the same specificity as enterocytes, while reduction of FATP4 expression in primary enterocytes by antisense oligonucleotides inhibited fatty acid uptake by 50%. These results suggested that FATP4 is the principal fatty acid transporter in enterocytes and may constitute a novel target for antiobesity therapy.

Organism species: Homo sapiens (Human)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant Fatty Acid Transport Protein 4 (FATP4) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to Fatty Acid Transport Protein 4 (FATP4) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to Fatty Acid Transport Protein 4 (FATP4) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for Fatty Acid Transport Protein 4 (FATP4) CLIA Kit Customized Service Offer
n/a ELISA Kit for Fatty Acid Transport Protein 4 (FATP4) ELISA Kit Customized Service Offer

Organism species: Mus musculus (Mouse)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant Fatty Acid Transport Protein 4 (FATP4) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to Fatty Acid Transport Protein 4 (FATP4) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to Fatty Acid Transport Protein 4 (FATP4) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for Fatty Acid Transport Protein 4 (FATP4) CLIA Kit Customized Service Offer
n/a ELISA Kit for Fatty Acid Transport Protein 4 (FATP4) ELISA Kit Customized Service Offer

Organism species: Rattus norvegicus (Rat)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant Fatty Acid Transport Protein 4 (FATP4) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to Fatty Acid Transport Protein 4 (FATP4) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to Fatty Acid Transport Protein 4 (FATP4) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for Fatty Acid Transport Protein 4 (FATP4) CLIA Kit Customized Service Offer
n/a ELISA Kit for Fatty Acid Transport Protein 4 (FATP4) ELISA Kit Customized Service Offer
  1. "Tissue distribution and cDNA cloning of a human fatty acid transport protein (hsFATP4)."Biochim. Biophys. Acta 1443:381-385(1998) [PubMed] [Europe PMC] [Abstract]
  2. "Complete sequencing and characterization of 21,243 full-length human cDNAs." Nat. Genet. 36:40-45(2004) [PubMed] [Europe PMC] [Abstract]
  3. "DNA sequence and analysis of human chromosome 9." Nature 429:369-374(2004) [PubMed] [Europe PMC] [Abstract]
  4. "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."Genome Res. 14:2121-2127(2004) [PubMed] [Europe PMC] [Abstract]
  5. "Initial characterization of the human central proteome."BMC Syst. Biol. 5:17-17(2011) [PubMed] [Europe PMC] [Abstract]
  6. "Genetic and structural evaluation of fatty acid transport protein-4 in relation to markers of the insulin resistance syndrome."J. Clin. Endocrinol. Metab. 89:392-399(2004) [PubMed] [Europe PMC] [Abstract]
  7. "Mutations in the fatty acid transport protein 4 gene cause the ichthyosis prematurity syndrome."Am. J. Hum. Genet. 85:248-253(2009) [PubMed] [Europe PMC] [Abstract]
  8. "A novel mutation in the fatty acid transport protein 4 gene in a patient initially described as affected by self-healing congenital verruciform hyperkeratosis."Am. J. Med. Genet. A 152:2664-2665(2010) [PubMed] [Europe PMC] [Abstract]