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S1PR2


Official Full Name
sphingosine-1-phosphate receptor 2
Organism
Homo sapiens
Gene ID
9294
Background
This gene encodes a member of the G protein-coupled receptors, as well as the EDG family of proteins. The encoded protein is a receptor for sphingosine 1-phosphate, which participates in cell proliferation, survival, and transcriptional activation. Defects in this gene have been associated with congenital profound deafness. [provided by RefSeq, Mar 2016]
Synonyms
EDG5; H218; LPB2; S1P2; AGR16; EDG-5; DFNB68; Gpcr13

Cat.No. Product Name Price
SHH401336 shRNA set against Human S1PR2 (NM_004230.3) Inquiry
SHH401340 shRNA set against Mouse S1PR2 (NM_010333.4) Inquiry
SHH023861 shRNA set against Human EDG5(NM_004230.3) Inquiry
SHH023879 shRNA set against Mouse Edg5(NM_010333.4) Inquiry
SHH023897 shRNA set against Rat Edg5(NM_017192.1) Inquiry
SHH390272 shRNA set against Human RAVER2 (NM_018211.3) Inquiry
SHH390276 shRNA set against Mouse RAVER2 (NM_183024.1) Inquiry
SHH401344 shRNA set against Rat S1PR2 (NM_017192.1) Inquiry
SHR167370 shRNA set against Mouse Raver2(NM_183024.1) Inquiry
SHW013340 shRNA set against Danio rerio S1PR2 (NM_001159970) Inquiry
Cat.No. Product Name Price
OE-PNDC000188 Human S1PR2 Nanodisc Inquiry
Cat.No. Product Name Price
CDCH396440 Human RAVER2 ORF clone(NM_018211.3) Inquiry
CDCR248819 Mouse S1pr2 ORF Clone(NM_010333.4) Inquiry
CDFR011244 Rat S1pr2 cDNA Clone(NM_017192.1) Inquiry
MiUTR1H-03107 S1PR2 miRNA 3'UTR clone Inquiry
MiUTR1M-04168 S1PR2 miRNA 3'UTR clone Inquiry
MiUTR1M-09960 RAVER2 miRNA 3'UTR clone Inquiry
MiUTR1R-01644 S1PR2 miRNA 3'UTR clone Inquiry
MiUTR4H-TG07353 RAVER2 miRNA 3'UTR clone Inquiry
CDCB174815 Danio rerio S1PR2 ORF Clone (NM_001159970) Inquiry
CDCB186036 Rabbit RAVER2 ORF clone (XM_008265122.1) Inquiry
CDCB195599 Rabbit S1PR2 ORF clone (XM_008250738.1) Inquiry
CDCH072006 Mouse Raver2 ORF clone (NM_183024.1) Inquiry
CDCH396442 Rat RAVER2 ORF clone(NM_001191867.1) Inquiry
CDCL186054 Human S1PR2 ORF clone(NM_004230.3) Inquiry
CDCR378258 Rat S1pr2 ORF Clone(NM_017192.1) Inquiry
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