Description: WB, IHC, ELISA

Description: WB, ELISA

Description: WB, ELISA

Description: WB, ELISA

Description: WB, ELISA

Description: A polyclonal antibody for detection of OAT1 from Human, Mouse, Rat. This OAT1 antibody is for WB, IHC-P, ELISA. It is affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from the Internal region of human OAT1

Description: A polyclonal antibody for detection of OAT1 from Human, Mouse, Rat. This OAT1 antibody is for WB, IHC-P, ELISA. It is affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from the Internal region of human OAT1

Description: A polyclonal antibody for detection of OAT1 from Human, Mouse, Rat. This OAT1 antibody is for WB, IHC-P, ELISA. It is affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from the Internal region of human OAT1

Description: A polyclonal antibody for detection of OAT1 from Human, Mouse, Rat. This OAT1 antibody is for WB, ELISA. It is affinity-purified from rabbit serum by affinity-chromatography using the specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from part region of human OAT1 protein

Description: A polyclonal antibody for detection of OAT1 from Human, Mouse, Rat. This OAT1 antibody is for WB, ELISA. It is affinity-purified from rabbit serum by affinity-chromatography using the specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from part region of human OAT1 protein

Description: A polyclonal antibody for detection of OAT1 from Human, Mouse, Rat. This OAT1 antibody is for WB, ELISA. It is affinity-purified from rabbit serum by affinity-chromatography using the specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from part region of human OAT1 protein

Description: A polyclonal antibody for detection of OAT1 from Human. This OAT1 antibody is for WB, ELISA. It is affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from the N-terminal region of human OAT1

Description: A polyclonal antibody for detection of OAT1 from Human. This OAT1 antibody is for WB, ELISA. It is affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from the N-terminal region of human OAT1

Description: A polyclonal antibody for detection of OAT1 from Human. This OAT1 antibody is for WB, ELISA. It is affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from the N-terminal region of human OAT1

Description: Multiple cysteine residues are necessary for proper targeting to the plasma membrane.|Involved in the renal elimination of endogenous and exogenous organic anions. Functions as organic anion exchanger when the uptake of one molecule of organic anion is coupled with an efflux of one molecule of endogenous dicarboxylic acid (glutarate| ketoglutarate| etc). Mediates the sodium-independent uptake of 2|3-dimercapto-1-propanesulfonic acid (DMPS) (By similarity). Mediates the sodium-independent uptake of p-aminohippurate (PAH)| ochratoxin (OTA)| acyclovir (ACV)| 3'-azido-3-'deoxythymidine (AZT)| cimetidine (CMD)| 2|4-dichloro-phenoxyacetate (2|4-D)| hippurate (HA)| indoleacetate (IA)| indoxyl sulfate (IS) and 3-carboxy-4-methyl-5-propyl-2-furanpropionate (CMPF)| cidofovir| adefovir| 9-(2-phosphonylmethoxyethyl) guanine (PMEG)| 9-(2-phosphonylmethoxyethyl) diaminopurine (PMEDAP) and edaravone sulfate. PAH uptake is inhibited by p-chloromercuribenzenesulphonate (PCMBS)| diethyl pyrocarbonate (DEPC)| sulindac| diclofenac| carprofen| glutarate and okadaic acid (By similarity). PAH uptake is inhibited by benzothiazolylcysteine (BTC)| S-chlorotrifluoroethylcysteine (CTFC)| cysteine S-conjugates S-dichlorovinylcysteine (DCVC)| furosemide| steviol| phorbol 12-myristate 13-acetate (PMA)| calcium ionophore A23187| benzylpenicillin| furosemide| indomethacin| bumetamide| losartan| probenecid| phenol red| urate| and alpha-ketoglutarate.|PTM:Glycosylated. Glycosylation at Asn-113 may occur at a secondary level. Glycosylation is necesssary for proper targeting of the transporter to the plasma membrane.|Belongs to the major facilitator superfamily. Organic cation transporter family.|tissue specificity:Strongly expressed in kidney and to a lower extent in liver| skeletal muscle| brain and placenta. Found at the basolateral membrane of the proximal tubule.|

Description: Multiple cysteine residues are necessary for proper targeting to the plasma membrane.|Involved in the renal elimination of endogenous and exogenous organic anions. Functions as organic anion exchanger when the uptake of one molecule of organic anion is coupled with an efflux of one molecule of endogenous dicarboxylic acid (glutarate| ketoglutarate| etc). Mediates the sodium-independent uptake of 2|3-dimercapto-1-propanesulfonic acid (DMPS) (By similarity). Mediates the sodium-independent uptake of p-aminohippurate (PAH)| ochratoxin (OTA)| acyclovir (ACV)| 3'-azido-3-'deoxythymidine (AZT)| cimetidine (CMD)| 2|4-dichloro-phenoxyacetate (2|4-D)| hippurate (HA)| indoleacetate (IA)| indoxyl sulfate (IS) and 3-carboxy-4-methyl-5-propyl-2-furanpropionate (CMPF)| cidofovir| adefovir| 9-(2-phosphonylmethoxyethyl) guanine (PMEG)| 9-(2-phosphonylmethoxyethyl) diaminopurine (PMEDAP) and edaravone sulfate. PAH uptake is inhibited by p-chloromercuribenzenesulphonate (PCMBS)| diethyl pyrocarbonate (DEPC)| sulindac| diclofenac| carprofen| glutarate and okadaic acid (By similarity). PAH uptake is inhibited by benzothiazolylcysteine (BTC)| S-chlorotrifluoroethylcysteine (CTFC)| cysteine S-conjugates S-dichlorovinylcysteine (DCVC)| furosemide| steviol| phorbol 12-myristate 13-acetate (PMA)| calcium ionophore A23187| benzylpenicillin| furosemide| indomethacin| bumetamide| losartan| probenecid| phenol red| urate| and alpha-ketoglutarate.|PTM:Glycosylated. Glycosylation at Asn-113 may occur at a secondary level. Glycosylation is necesssary for proper targeting of the transporter to the plasma membrane.|Belongs to the major facilitator superfamily. Organic cation transporter family.|tissue specificity:Strongly expressed in kidney and to a lower extent in liver| skeletal muscle| brain and placenta. Found at the basolateral membrane of the proximal tubule.|

Description: Multiple cysteine residues are necessary for proper targeting to the plasma membrane.|Involved in the renal elimination of endogenous and exogenous organic anions. Functions as organic anion exchanger when the uptake of one molecule of organic anion is coupled with an efflux of one molecule of endogenous dicarboxylic acid (glutarate| ketoglutarate| etc). Mediates the sodium-independent uptake of 2|3-dimercapto-1-propanesulfonic acid (DMPS) (By similarity). Mediates the sodium-independent uptake of p-aminohippurate (PAH)| ochratoxin (OTA)| acyclovir (ACV)| 3'-azido-3-'deoxythymidine (AZT)| cimetidine (CMD)| 2|4-dichloro-phenoxyacetate (2|4-D)| hippurate (HA)| indoleacetate (IA)| indoxyl sulfate (IS) and 3-carboxy-4-methyl-5-propyl-2-furanpropionate (CMPF)| cidofovir| adefovir| 9-(2-phosphonylmethoxyethyl) guanine (PMEG)| 9-(2-phosphonylmethoxyethyl) diaminopurine (PMEDAP) and edaravone sulfate. PAH uptake is inhibited by p-chloromercuribenzenesulphonate (PCMBS)| diethyl pyrocarbonate (DEPC)| sulindac| diclofenac| carprofen| glutarate and okadaic acid (By similarity). PAH uptake is inhibited by benzothiazolylcysteine (BTC)| S-chlorotrifluoroethylcysteine (CTFC)| cysteine S-conjugates S-dichlorovinylcysteine (DCVC)| furosemide| steviol| phorbol 12-myristate 13-acetate (PMA)| calcium ionophore A23187| benzylpenicillin| furosemide| indomethacin| bumetamide| losartan| probenecid| phenol red| urate| and alpha-ketoglutarate.|PTM:Glycosylated. Glycosylation at Asn-113 may occur at a secondary level. Glycosylation is necesssary for proper targeting of the transporter to the plasma membrane.|Belongs to the major facilitator superfamily. Organic cation transporter family.|tissue specificity:Strongly expressed in kidney and to a lower extent in liver| skeletal muscle| brain and placenta. Found at the basolateral membrane of the proximal tubule.|

Description: Multiple cysteine residues are necessary for proper targeting to the plasma membrane.,Involved in the renal elimination of endogenous and exogenous organic anions. Functions as organic anion exchanger when the uptake of one molecule of organic anion is coupled with an efflux of one molecule of endogenous dicarboxylic acid (glutarate, ketoglutarate, etc). Mediates the sodium-independent uptake of 2,3-dimercapto-1-propanesulfonic acid (DMPS) (By similarity). Mediates the sodium-independent uptake of p-aminohippurate (PAH), ochratoxin (OTA), acyclovir (ACV), 3'-azido-3-'deoxythymidine (AZT), cimetidine (CMD), 2,4-dichloro-phenoxyacetate (2,4-D), hippurate (HA), indoleacetate (IA), indoxyl sulfate (IS) and 3-carboxy-4-methyl-5-propyl-2-furanpropionate (CMPF), cidofovir, adefovir, 9-(2-phosphonylmethoxyethyl) guanine (PMEG), 9-(2-phosphonylmethoxyethyl) diaminopurine (PMEDAP) and edaravone sulfate. PAH uptake is inhibited by p-chloromercuribenzenesulphonate (PCMBS), diethyl pyrocarbonate (DEPC), sulindac, diclofenac, carprofen, glutarate and okadaic acid (By similarity). PAH uptake is inhibited by benzothiazolylcysteine (BTC), S-chlorotrifluoroethylcysteine (CTFC), cysteine S-conjugates S-dichlorovinylcysteine (DCVC), furosemide, steviol, phorbol 12-myristate 13-acetate (PMA), calcium ionophore A23187, benzylpenicillin, furosemide, indomethacin, bumetamide, losartan, probenecid, phenol red, urate, and alpha-ketoglutarate.,PTM:Glycosylated. Glycosylation at Asn-113 may occur at a secondary level. Glycosylation is necesssary for proper targeting of the transporter to the plasma membrane.,Belongs to the major facilitator superfamily. Organic cation transporter family.,tissue specificity:Strongly expressed in kidney and to a lower extent in liver, skeletal muscle, brain and placenta. Found at the basolateral membrane of the proximal tubule.,

Description: Multiple cysteine residues are necessary for proper targeting to the plasma membrane.,Involved in the renal elimination of endogenous and exogenous organic anions. Functions as organic anion exchanger when the uptake of one molecule of organic anion is coupled with an efflux of one molecule of endogenous dicarboxylic acid (glutarate, ketoglutarate, etc). Mediates the sodium-independent uptake of 2,3-dimercapto-1-propanesulfonic acid (DMPS) (By similarity). Mediates the sodium-independent uptake of p-aminohippurate (PAH), ochratoxin (OTA), acyclovir (ACV), 3'-azido-3-'deoxythymidine (AZT), cimetidine (CMD), 2,4-dichloro-phenoxyacetate (2,4-D), hippurate (HA), indoleacetate (IA), indoxyl sulfate (IS) and 3-carboxy-4-methyl-5-propyl-2-furanpropionate (CMPF), cidofovir, adefovir, 9-(2-phosphonylmethoxyethyl) guanine (PMEG), 9-(2-phosphonylmethoxyethyl) diaminopurine (PMEDAP) and edaravone sulfate. PAH uptake is inhibited by p-chloromercuribenzenesulphonate (PCMBS), diethyl pyrocarbonate (DEPC), sulindac, diclofenac, carprofen, glutarate and okadaic acid (By similarity). PAH uptake is inhibited by benzothiazolylcysteine (BTC), S-chlorotrifluoroethylcysteine (CTFC), cysteine S-conjugates S-dichlorovinylcysteine (DCVC), furosemide, steviol, phorbol 12-myristate 13-acetate (PMA), calcium ionophore A23187, benzylpenicillin, furosemide, indomethacin, bumetamide, losartan, probenecid, phenol red, urate, and alpha-ketoglutarate.,PTM:Glycosylated. Glycosylation at Asn-113 may occur at a secondary level. Glycosylation is necesssary for proper targeting of the transporter to the plasma membrane.,Belongs to the major facilitator superfamily. Organic cation transporter family.,tissue specificity:Strongly expressed in kidney and to a lower extent in liver, skeletal muscle, brain and placenta. Found at the basolateral membrane of the proximal tubule.,

Description: Multiple cysteine residues are necessary for proper targeting to the plasma membrane.,Involved in the renal elimination of endogenous and exogenous organic anions. Functions as organic anion exchanger when the uptake of one molecule of organic anion is coupled with an efflux of one molecule of endogenous dicarboxylic acid (glutarate, ketoglutarate, etc). Mediates the sodium-independent uptake of 2,3-dimercapto-1-propanesulfonic acid (DMPS) (By similarity). Mediates the sodium-independent uptake of p-aminohippurate (PAH), ochratoxin (OTA), acyclovir (ACV), 3'-azido-3-'deoxythymidine (AZT), cimetidine (CMD), 2,4-dichloro-phenoxyacetate (2,4-D), hippurate (HA), indoleacetate (IA), indoxyl sulfate (IS) and 3-carboxy-4-methyl-5-propyl-2-furanpropionate (CMPF), cidofovir, adefovir, 9-(2-phosphonylmethoxyethyl) guanine (PMEG), 9-(2-phosphonylmethoxyethyl) diaminopurine (PMEDAP) and edaravone sulfate. PAH uptake is inhibited by p-chloromercuribenzenesulphonate (PCMBS), diethyl pyrocarbonate (DEPC), sulindac, diclofenac, carprofen, glutarate and okadaic acid (By similarity). PAH uptake is inhibited by benzothiazolylcysteine (BTC), S-chlorotrifluoroethylcysteine (CTFC), cysteine S-conjugates S-dichlorovinylcysteine (DCVC), furosemide, steviol, phorbol 12-myristate 13-acetate (PMA), calcium ionophore A23187, benzylpenicillin, furosemide, indomethacin, bumetamide, losartan, probenecid, phenol red, urate, and alpha-ketoglutarate.,PTM:Glycosylated. Glycosylation at Asn-113 may occur at a secondary level. Glycosylation is necesssary for proper targeting of the transporter to the plasma membrane.,Belongs to the major facilitator superfamily. Organic cation transporter family.,tissue specificity:Strongly expressed in kidney and to a lower extent in liver, skeletal muscle, brain and placenta. Found at the basolateral membrane of the proximal tubule.,

Description: Solute carrier family 22 member 6 encoded by SLC22A6 is involved in the sodium-dependent transport and excretion of organic anions, some of which are potentially toxic. The encoded protein is an integral membrane protein and may be localized to the basolateral membrane. Four transcript variants encoding four different isoforms have been found for this gene.

Description: Solute carrier family 22 member 6 encoded by SLC22A6 is involved in the sodium-dependent transport and excretion of organic anions, some of which are potentially toxic. The encoded protein is an integral membrane protein and may be localized to the basolateral membrane. Four transcript variants encoding four different isoforms have been found for this gene.

Description: Solute carrier family 22 member 6 encoded by SLC22A6 is involved in the sodium-dependent transport and excretion of organic anions, some of which are potentially toxic. The encoded protein is an integral membrane protein and may be localized to the basolateral membrane. Four transcript variants encoding four different isoforms have been found for this gene.

Description: Available in various conjugation types.

Description: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide, pH 7.3.