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SLC27A4


Official Full Name
solute carrier family 27 member 4
Organism
Homo sapiens
Gene ID
10999
Background
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. [provided by RefSeq, Apr 2010]
Synonyms
IPS; FATP4; ACSVL4

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SHH410076 shRNA set against Human SLC27A4 (NM_005094.3) Inquiry
SHH410080 shRNA set against Mouse SLC27A4 (NM_011989.4) Inquiry
SHL005090 shRNA set against Mouse Slc27a4(NM_011989.4) Inquiry
SHW008374 shRNA set against Danio rerio SLC27A4 (NM_001017737) Inquiry
Cat.No. Product Name Price
MiUTR1M-10832 SLC27A4 miRNA 3'UTR clone Inquiry
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SKO0783 SLC27A4 Validated sgRNA vector Inquiry
CDCB159596 Human SLC27A4 ORF clone (BC009959) Inquiry
CDCB169849 Danio rerio SLC27A4 ORF Clone (NM_001017737) Inquiry
CDCB186544 Rabbit SLC27A4 ORF clone (XM_002722970.2) Inquiry
CDCS412091 Human SLC27A4 ORF Clone (BC009959) Inquiry
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