ARG43401

anti-SLCO1B3 / OATP1B3 antibody

anti-SLCO1B3 / OATP1B3 antibody for Western blot and Human

Overview

Product Description Rabbit Polyclonal antibody recognizes SLCO1B3 / OATP1B3
Tested Reactivity Hu
Tested Application WB
Host Rabbit
Clonality Polyclonal
Isotype IgG
Target Name SLCO1B3 / OATP1B3
Antigen Species Human
Immunogen KLH-conjugated synthetic peptide between aa. 639-668 of Human SLCO1B3 / OATP1B3.
Conjugation Un-conjugated
Alternate Names Organic anion-transporting polypeptide 8; LST3; Liver-specific organic anion transporter 2; OATP1B3; LST-3TM13; HBLRR; LST-2; SLC21A8; Solute carrier family 21 member 8; Organic anion transporter 8; OATP-8; Solute carrier organic anion transporter family member 1B3; OATP8

Application Instructions

Application Suggestion
Tested Application Dilution
WB1:2000
Application Note * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.
Positive Control HeLa and NCI-H460
Observed Size 85, 110-120 kDa

Properties

Form Liquid
Purification Purification with Protein A and immunogen peptide.
Buffer PBS and 0.09% (W/V) Sodium azide.
Preservative 0.09% (W/V) Sodium azide
Storage Instruction For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
Note For laboratory research only, not for drug, diagnostic or other use.

Bioinformation

Database Links

GeneID: 28234 Human SLCO1B3

Swiss-port # Q9NPD5 Human Solute carrier organic anion transporter family member 1B3

Gene Symbol SLCO1B3
Gene Full Name solute carrier organic anion transporter family, member 1B3
Background This gene encodes a liver-specific member of the organic anion transporter family. The encoded protein is a transmembrane receptor that mediates the sodium-independent uptake of endogenous and xenobiotic compounds and plays a critical role in bile acid and bilirubin transport. Mutations in this gene are a cause of Rotor type hyperbilirubinemia. Alternative splicing of this gene and the use of alternative promoters results in transcript variants encoding different isoforms that differ in their tissue specificity. [provided by RefSeq, Mar 2017]
Function Mediates the Na(+)-independent uptake of organic anions such as 17-beta-glucuronosyl estradiol, taurocholate, triiodothyronine (T3), leukotriene C4, dehydroepiandrosterone sulfate (DHEAS), methotrexate and sulfobromophthalein (BSP). Involved in the clearance of bile acids and organic anions from the liver. [UniProt]
Cellular Localization Basolateral cell membrane; Multi-pass membrane protein. [UniProt]
Calculated MW 77 kDa
PTM N-glycosylated. [UniProt]