Solute Carrier Organic Anion Transporter Family, Member 2A1 (SLCO2A1)

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PGT; OATP2A1; SLC21A2; MATR1; Solute Carrier Family 21 Member 2; Prostaglandin Transporter; Matrin F/G 1

Solute Carrier Organic Anion Transporter Family, Member 2A1 (SLCO2A1)
Lu et al. (1996) screened a human kidney cDNA library and isolated human PGT. The deduced 643-amino acid protein shares 82% identity with the rat protein. It contains 12 putative transmembrane domains and 3 N-glycosylation sites. Northern blot analysis detected wide PGT distribution, with transcripts ranging from 2.1 to 10 kb. Transcripts of 4.4 to 5.1 kb, often appearing as a doublet, were expressed in most adult tissues and all fetal tissues examined. Lu et al. (1996) noted that the tissue distribution of PGT transcripts was substantially broader, and the variety of PGT transcripts was greater, in human compared with rat. First, PGT might mediate the efflux of newly synthesized PGs from cells. Second, PGT might mediate epithelial PG transport. A third possible role of PGT is that of mediating PG clearance and degradation.

Organism species: Homo sapiens (Human)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant Solute Carrier Organic Anion Transporter Family, Member 2A1 (SLCO2A1) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to Solute Carrier Organic Anion Transporter Family, Member 2A1 (SLCO2A1) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to Solute Carrier Organic Anion Transporter Family, Member 2A1 (SLCO2A1) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for Solute Carrier Organic Anion Transporter Family, Member 2A1 (SLCO2A1) CLIA Kit Customized Service Offer
n/a ELISA Kit for Solute Carrier Organic Anion Transporter Family, Member 2A1 (SLCO2A1) ELISA Kit Customized Service Offer

Organism species: Mus musculus (Mouse)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant Solute Carrier Organic Anion Transporter Family, Member 2A1 (SLCO2A1) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to Solute Carrier Organic Anion Transporter Family, Member 2A1 (SLCO2A1) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to Solute Carrier Organic Anion Transporter Family, Member 2A1 (SLCO2A1) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for Solute Carrier Organic Anion Transporter Family, Member 2A1 (SLCO2A1) CLIA Kit Customized Service Offer
n/a ELISA Kit for Solute Carrier Organic Anion Transporter Family, Member 2A1 (SLCO2A1) ELISA Kit Customized Service Offer

Organism species: Rattus norvegicus (Rat)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant Solute Carrier Organic Anion Transporter Family, Member 2A1 (SLCO2A1) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to Solute Carrier Organic Anion Transporter Family, Member 2A1 (SLCO2A1) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to Solute Carrier Organic Anion Transporter Family, Member 2A1 (SLCO2A1) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for Solute Carrier Organic Anion Transporter Family, Member 2A1 (SLCO2A1) CLIA Kit Customized Service Offer
n/a ELISA Kit for Solute Carrier Organic Anion Transporter Family, Member 2A1 (SLCO2A1) ELISA Kit Customized Service Offer
  1. "Cloning, in vitro expression, and tissue distribution of a human prostaglandin transporter cDNA(hPGT)."J. Clin. Invest. 98:1142-1149(1996) [PubMed] [Europe PMC] [Abstract]
  2. "Molecular cloning of the gene for the human prostaglandin transporter hPGT: gene organization, promoter activity, and chromosomal localization."Biochem. Biophys. Res. Commun. 246:805-812(1998) [PubMed] [Europe PMC] [Abstract]
  3. "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."Genome Res. 14:2121-2127(2004) [PubMed] [Europe PMC] [Abstract]
  4. "Mutations in the prostaglandin transporter encoding gene SLCO2A1 cause primary hypertrophic osteoarthropathy and isolated digital clubbing."Hum. Mutat. 33:660-664(2012) [PubMed] [Europe PMC] [Abstract]
  5. "N-terminal acetylome analyses and functional insights of the N-terminal acetyltransferase NatB."Proc. Natl. Acad. Sci. U.S.A. 109:12449-12454(2012) [PubMed] [Europe PMC] [Abstract]
  6. "Exome sequencing identifies SLCO2A1 mutations as a cause of primary hypertrophic osteoarthropathy."Am. J. Hum. Genet. 90:125-132(2012) [PubMed] [Europe PMC] [Abstract]
  7. "Prostaglandin transporter mutations cause pachydermoperiostosis with myelofibrosis." Hum. Mutat. 33:1175-1181(2012) [PubMed] [Europe PMC] [Abstract]
  8. "Mutations in the prostaglandin transporter SLCO2A1 cause primary hypertrophic osteoarthropathy with digital clubbing."J. Invest. Dermatol. 132:2473-2476(2012) [PubMed] [Europe PMC] [Abstract]