Main InformationTargetOCT1Host SpeciesRabbitReactivityHuman, Rat, Mouse,ApplicationsIHC, IF, WBMW61kD (Observed)Conjugate/ModificationUnmodifiedDetailed InformationRecommended Dilution RatioIHC 1:50-200; WB 1:500-2000; IF 1:50-200FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.SpecificityThis antibody detects endogenous levels of human OCT1 Monoclonal AntibodyPurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.Storage-15°C to -25°C/1 year(Do not lower than -25°C)Concentration1 mg/mlMW(Observed)61kDModificationUnmodifiedClonalityPolyclonalIsotypeIgGAntigen&Target InformationImmunogen:Synthesized peptide derived from human OCT1 Monoclonal AntibodySpecificity:This antibody detects endogenous levels of human OCT1 Monoclonal AntibodyGene Name:SLC22A1 OCT1Protein Name:45200Other Name:Solute carrier family 22 member 1 ; Organic cation transporter 1 ; hOCT1 ;Background: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. Two transcript variants encoding two different isoforms have been found for this gene, but only the longer variant encodes a functional transporter. [provided by RefSeq, Jul 2008],Function:Caution:The sequence shown here is derived from an Ensembl automatic analysis pipeline and should be considered as preliminary data.,Function:Translocates a broad array of organic cations with various structures and molecular weights including the model compounds 1-methyl-4-phenylpyridinium (MPP), tetraethylammonium (TEA), N-1-methylnicotinamide (NMN), 4-(4-(dimethylamino)styryl)-N-methylpyridinium (ASP), the endogenous compounds choline, guanidine, histamine, epinephrine, adrenaline, noradrenaline and dopamine, and the drugs quinine, and metformin. The transport of organic cations is inhibited by a broad array of compounds like tetramethylammonium (TMA), cocaine, lidocaine, NMDA receptor antagonists, atropine, prazosin, cimetidine, TEA and NMN, guanidine, cimetidine, choline, procainamide, quinine, tetrabutylammonium, and tetrapentylammonium. Translocates organic cations in an electrogenic and pH-independent manner. Translocates organic cations across the plasma membrane in both directions. Transports the polyamines spermine and spermidine. Transports pramipexole across the basolateral membrane of the proximal tubular epithelial cells. The choline transport is activated by MMTS. Regulated by various intracellular signaling pathways including inhibition by protein kinase A activation, and endogenously activation by the calmodulin complex, the calmodulin-dependent kinase II and LCK tyrosine kinase.,induction:In the liver activated by HNF4A and suppressed by bile acids via NR0B2. Increased by cholesterol treatment in hepatocyte cells.,PTM:Phosphorylated.,similarity:Belongs to the major facilitator superfamily. Organic cation transporter family.,tissue specificity:Widely expressed with high level in liver. Isoform 1 and isoform 2 are expressed in liver. Isoform 1, isoform 2, isoform 3 and isoform 4 are expressed in glial cell lines.,Cellular Localization:Basolateral cell membrane ; Multi-pass membrane protein .Tissue Expression:Widely expressed with high level in liver. Isoform 1 and isoform 2 are expressed in liver. Isoform 1, isoform 2, isoform 3 and isoform 4 are expressed in glial cell lines.Research Areas:>>Bile secretion ; >>Choline metabolism in cancer
商品信息已成功复制,启研竭诚为您服务
