尿酸盐重吸收转运子1抗体
规格：1mg/1ml
英文名： SLC22A12
别名： URAT1; S22AC_HUMAN; OAT4L; Solute carrier family 22 member 12; Organic anion transporter 4-like protein; Renal-specific transporter; RST; Urate anion exchanger 1; Urate 1 transporter protein; solute c
分子量： 61kDa
储存液：0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glyce
克隆类型：Polyclonal
亚型：IgG
纯化方法：affinity purified by Protein A
**原：KLH conjugated synthetic peptide derived from human URAT1
交叉反应：Human,
细胞定位：细胞膜
尿酸盐重吸收转运子1抗体产品介绍：background: URAT1 Recent advances in molecular biology have identified three organic anion transporter families: the organic anion transporter (OAT) family encoded by SLC22A, the organic anion transporting peptide (OATP) family encoded by SLC21A (SLCO), and the multidrug resistance-associated protein (MRP) family encoded by ABCC. These families play critical roles in the transepithelial transport of organic anions in the kidneys as well as in other tissues such as the liver and brain. Among these families, the OAT family plays the central role in renal organic anion transport. Knowledge of these three families at the molecular level, 尿酸盐重吸收转运子1抗体such as substrate selectivity, tissue distribution, and gene localization, is rapidly increasing. Function: Required for efficient urate re-absorption in the kidney. Regulates blood urate levels. Mediates saturable urate uptake by facilitating the exchange of urate against organic anions. Subunit: Interacts with PDZK1. Subcellular Location: Cell membrane; Multi-pass membrane protein. Note=Detected in the luminal membrane of the epithelium of renal proximal tubules. Tissue Specificity: Detected in kidney (at protein level). Detected in fetal and ***** kidney. Detected in epithelial cells of proximal tubules in renal cortex. DISEASE: Hypouricemia renal 1 (RHUC1) [MIM:220150]: A disorder characterized by impaired uric acid reabsorption at the apical membrane of proximal renal tubule cells, and high urinary urate excretion. Patients often appear asymptomatic, but may be subject to 尿酸盐重吸收转运子1抗体exercise-induced acute renal failure, chronic renal dysfunction and nephrolithiasis. Note=The disease is caused by mutations affecting the gene represented in this entry. Similarity: Belongs to the major facilitator (TC 2.A.1) superfamily. Organic cation transporter (TC 2.A.1.19) family. Gene ID: 55867 Database links: Entrez Gene: 55867 Human Omim: 607097 Human SwissProt: Q9NSA0 Human Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
尿酸盐重吸收转运子1抗体产品应用：WB=1:100-500 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500 （石蜡切片需做抗原修复） not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user.
研究领域：转运蛋白 跨膜蛋白
储存条件： Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
来源： Rabbit
外观： Lyophilized or Liquid