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SLC27A4 Antibody (monoclonal) (M01)

Mouse monoclonal antibody raised against a full length recombinant SLC27A4.

  • WB - SLC27A4 Antibody (monoclonal) (M01) AT3917a
    Antibody Reactive Against Recombinant Protein.Western Blot detection against Immunogen (51.81 KDa) .
  • WB - SLC27A4 Antibody (monoclonal) (M01) AT3917a
    SLC27A4 monoclonal antibody (M01), clone 1F4-1B10 Western Blot analysis of SLC27A4 expression in HeLa ( (Cat # AT3917a )
  • E - SLC27A4 Antibody (monoclonal) (M01) AT3917a
    Detection limit for recombinant GST tagged SLC27A4 is 0.1 ng/ml as a capture antibody.
Product Information
  • Applications Legend:
  • WB=Western Blot
  • IHC=Immunohistochemistry
  • IHC-P=Immunohistochemistry (Paraffin-embedded Sections)
  • IHC-F=Immunohistochemistry (Frozen Sections)
  • IF=Immunofluorescence
  • FC=Flow Cytopmetry
  • IC=Immunochemistry
  • ICC=Immunocytochemistry
  • IP=Immunoprecipitation
  • DB=Dot Blot
  • CHIP=Chromatin Immunoprecipitation
  • FA=Fluorescence Assay
  • IEM=Immunoelectronmicroscopy
  • EIA=Enzyme Immunoassay
Primary Accession Q6P1M0
Other Accession BC009959
Reactivity Human
Host mouse
Clonality Monoclonal
Isotype IgG1 kappa
Clone Names 1F4-1B10
Calculated MW 72064 Da
Additional Information
Gene ID 10999
Other Names Long-chain fatty acid transport protein 4, FATP-4, Fatty acid transport protein 4, 621-, Solute carrier family 27 member 4, SLC27A4, ACSVL4, FATP4
Target/Specificity SLC27A4 (AAH09959.1, 1 a.a. ~ 237 a.a) full-length recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.
Dilution WB~~1:500~1000
Format Clear, colorless solution in phosphate buffered saline, pH 7.2 .
StorageStore at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
PrecautionsSLC27A4 Antibody (monoclonal) (M01) is for research use only and not for use in diagnostic or therapeutic procedures.
Research Areas
Citations (0)

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This gene 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. Mutations in this gene have been associated with ichthyosis prematurity syndrome.


1.Interactions between FATP4 and ichthyin in epidermal lipid processing may provide clues to the pathogenesis of autosomal recessive congenital ichthyosis.Li H, Vahlquist A, Torma H.J Dermatol Sci. 2012 Dec 13. pii: S0923-1811(12)00938-3. doi: 10.1016/j.jdermsci.2012.11.593.2.Adipokines promote lipotoxicity in human skeletal muscle cells.Taube A, Lambernd S, van Echten-Deckert G, Eckardt K, Eckel J.Arch Physiol Biochem. 2012 Jul;118(3):92-101. Epub 2012 Jun 12.3.Modulation of Fatty Acid Transport and Metabolism by Obesity in the Human Full-Term Placenta.Dube E, Gravel A, Martin C, Desparois G, Moussa I, Ethier-Chiasson M, Forest JC, Giguere Y, Masse A, Lafond J.Biol Reprod. 2012 May 2.4.Mutations in the Fatty Acid Transport Protein 4 Gene Cause the Ichthyosis Prematurity Syndrome.Klar J, Schweiger M, Zimmerman R, Zechner R, Li H, Torma H, Vahlquist A, Bouadjar B, Dahl N, Fischer J.Am J Hum Genet. 2009 Aug;85(2):248-53. Epub 2009 Jul 23.5.Fatty acid transport and activation and the expression patterns of genes involved in fatty acid trafficking.Sandoval A, Fraisl P, Arias-Barrau E, DiRusso CD, Singer D, Sealls W, Black PN.Arch Biochem Biophys. 2008 Sep 15;477(2):363-71. Epub 2008 Jun 20.

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$ 350.00
Cat# AT3917a
Availability: 7-10 days
Bulk Size
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