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SLC27A3


Official Full Name
solute carrier family 27 member 3
Organism
Homo sapiens
Gene ID
11000
Background
This gene belongs to a family of integral membrane proteins and encodes a protein that is involved in lipid metabolism. The increased expression of this gene in human neural stem cells derived from induced pluripotent stem cells suggests that it plays an important role in early brain development. Naturally occurring mutations in this gene are associated with autism spectrum disorders. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2017]
Synonyms
FATP3; ACSVL3; VLCS-3

Cat.No. Product Name Price
SHH410064 shRNA set against Human SLC27A3 (NM_024330.1) Inquiry
SHH410068 shRNA set against Mouse SLC27A3 (NM_011988.2) Inquiry
SHH410072 shRNA set against Rat SLC27A3 (NM_001106439.1) Inquiry
Cat.No. Product Name Price
CDCH081740 human SLC27A3 ORF clone (NM_024330.1) Inquiry
CDFG004325 Human SLC27A3 cDNA Clone(NM_024330.1) Inquiry
CDFR006174 Rat Slc27a3 cDNA Clone(NM_001106439.1) Inquiry
MiUTR1H-09504 SLC27A3 miRNA 3'UTR clone Inquiry
CDCB193116 Rabbit SLC27A3 ORF clone (XM_002715490.2) Inquiry
CDCH081744 Mouse Slc27a3 ORF clone (NM_011988.2) Inquiry
CDCR373226 Rat Slc27a3 ORF Clone(NM_001106439.1) Inquiry
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