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SLC22A3

  • Official Full Name

    solute carrier family 22 (organic cation transporter), member 3

  • Overview

    Polyspecific organic cation transporters in the liver, kidney, intestine, and other organs are critical for elimination of many endogenous small organic cations as well as a wide array of drugs and environmental toxins. This gene is one of three similar cation transporter genes located in a cluster on chromosome 6. The encoded protein contains twelve putative transmembrane domains and is a plasma integral membrane protein. [provided by RefSeq, Jul 2008]
  • Synonyms

    SLC22A3; solute carrier family 22 (organic cation transporter), member 3; EMT; EMTH; OCT3; solute carrier family 22 member 3; organic cation transporter 3; EMT organic cation transporter 3; extraneuronal monoamine transporter; solute carrier family 22 (extraneuronal monoamine transporter), member 3;

  • Recombinant Proteins
  • Protein Pre-coupled Magnetic Beads
  • Homo sapiens (Human)
  • Human
  • Mus musculus (Mouse)
  • Rat
  • Rattus norvegicus (Rat)
  • E.coli expression system
  • HEK293
  • Mammalian Cell
  • Wheat Germ
  • His
  • His (Fc)
  • Avi
  • N/A
Species Cat.# Product name Source (Host) Tag Protein Length Price
Human SLC22A3-31412TH Recombinant Human SLC22A3 Wheat Germ N/A 66 amino acids
Rat SLC22A3-5457R Recombinant Rat SLC22A3 Protein Mammalian Cell His
Rat SLC22A3-5116R-B Recombinant Rat SLC22A3 Protein Pre-coupled Magnetic Beads HEK293
Rat SLC22A3-5116R Recombinant Rat SLC22A3 Protein, His (Fc)-Avi-tagged HEK293 His (Fc)-Avi
Homo sapiens (Human) RFL12585HF Recombinant Full Length Human Solute Carrier Family 22 Member 3(Slc22A3) Protein, His-Tagged E.coli expression system His Full Length (1-556)
Mus musculus (Mouse) RFL26026MF Recombinant Full Length Mouse Solute Carrier Family 22 Member 3(Slc22A3) Protein, His-Tagged E.coli expression system His Full Length (1-551)
Rattus norvegicus (Rat) RFL23216RF Recombinant Full Length Rat Solute Carrier Family 22 Member 3(Slc22A3) Protein, His-Tagged E.coli expression system His Full Length (1-551)
  • Involved Pathway
  • Protein Function
  • Interacting Protein
  • SLC22A3 Related Articles

SLC22A3 involved in several pathways and played different roles in them. We selected most pathways SLC22A3 participated on our site, such as Choline metabolism in cancer, which may be useful for your reference. Also, other proteins which involved in the same pathway with SLC22A3 were listed below. Creative BioMart supplied nearly all the proteins listed, you can search them on our site.

Pathway Name Pathway Related Protein
Choline metabolism in cancerSOS1;PIK3CB;TSC1;EIF4EBP1;NRAS;DGKQ;AKT1;PRKCB;PDGFA

SLC22A3 has several biochemical functions, for example, dopamine transmembrane transporter activity, organic cation transmembrane transporter activity, protein binding. Some of the functions are cooperated with other proteins, some of the functions could acted by SLC22A3 itself. We selected most functions SLC22A3 had, and list some proteins which have the same functions with SLC22A3. You can find most of the proteins on our site.

Function Related Protein
dopamine transmembrane transporter activitySLC6A3;SLC22A1;SLC22A3;SLC22A2
organic cation transmembrane transporter activitySLC22A14;SLC22A2;SLC7A8;SLC22A1;SLC22A3
protein bindingTRIM59;UQCC2;ICAM3;SPTBN1;MRPL13;MAB21L3;PI4KA;PDCD5;GTF2A1
quaternary ammonium group transmembrane transporter activitySLC22A2;SLC22A1;SLC22A5;SLC22A3
toxin transporter activityABCG1;SLC17A3;SLC7A8;SLC22A2;SLC22A3;LRP6

SLC22A3 has direct interactions with proteins and molecules. Those interactions were detected by several methods such as yeast two hybrid, co-IP, pull-down and so on. We selected proteins and molecules interacted with SLC22A3 here. Most of them are supplied by our site. Hope this information will be useful for your research of SLC22A3.

ABL1; NCK1

Chu, SH; Zhou, ZM; et al. In vitro and in vivo radiosensitization of human glioma U251 cells induced by upregulated expression of SLC22A18. CANCER GENE THERAPY 21:103-109(2014).
Shibbani, K; Fahed, AC; et al. Primary carnitine deficiency: novel mutations and insights into the cardiac phenotype. CLINICAL GENETICS 85:127-137(2014).
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