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SLC13A5


Official Full Name
solute carrier family 13 member 5
Organism
Homo sapiens
Gene ID
284111
Background
This gene encodes a protein belonging to the solute carrier family 13 group of proteins. This family member is a sodium-dependent citrate cotransporter that may regulate metabolic processes. Mutations in this gene cause early infantile epileptic encephalopathy 25. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2014]
Synonyms
INDY; NACT; DEE25; mIndy; EIEE25

Cat.No. Product Name Price
SHH408464 shRNA set against Rat SLC13A5 (NM_170668.1) Inquiry
SHH408456 shRNA set against Human SLC13A5 (NM_177550.3) Inquiry
SHH408460 shRNA set against Mouse SLC13A5 (NM_001004148.4) Inquiry
SHR229052 shRNA set against Rat Slc13a5(NM_170668.1) Inquiry
Cat.No. Product Name Price
CDFG016263 Mouse Slc13a5 cDNA Clone(NM_001004148.4) Inquiry
CDFH017681 Human SLC13A5 cDNA Clone(NM_001143838.1) Inquiry
CDFR014678 Rat Slc13a5 cDNA Clone(NM_170668.1) Inquiry
MiUTR1R-07372 SLC13A5 miRNA 3'UTR clone Inquiry
MiUTR3H-09903 SLC13A5 miRNA 3'UTR clone Inquiry
MiUTR3H-09904 SLC13A5 miRNA 3'UTR clone Inquiry
CDCB180449 Rabbit SLC13A5 ORF clone (XM_008270859.1) Inquiry
CDCH080884 human SLC13A5 ORF clone (NM_001143838.1) Inquiry
CDCH400575 Human SLC13A5 ORF clone(NM_177550.3) Inquiry
CDCL226646 Mouse Slc13a5 ORF Clone(NM_001004148.4) Inquiry
CDCR381729 Rat Slc13a5 ORF Clone(NM_170668.1) Inquiry
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