ATP7A Antibody (RPE)抗体，orb1497

产品描述：Mouse monoclonal to Copper Transporting ATPase 1 (RPE). The copper efflux transporters ATP7A and ATP7B sequester intracellular copper into the vesicular secretory pathway for export from the cell. ATP7A (also known as Copper-transporting ATPase 1) functions as a transmembrane copper-trans locating P-type ATPase and plays a vital role in systemic copper absorption in the gut and copper reabsorption in the kidney. Polarized epithelial cells such as Madin-Darby canine kidney cells are a physiologically relevant model for systemic copper absorption and reabsorption in vivo. Although ATP7A is not detectable in most normal tissues, it is expressed in a considerable fraction of many common tumor types. Increased expression of ATP7A renders cells resistant to cisplatin and carboplatin. Mutations in the ATP7A gene result in Menkes disease, which is fatal in early childhood. Mutations in the ATP7B gene lead to the autosomal recessive disorder, Wilson disease, characterized by neurological symptoms and hepatic damage..

别名:ATP7A, ATP 7A, ATP7A_HUMAN, ATPase Cu transporting, ATPase copper transporting alpha polypeptide, ATPase Cu++ transporting alpha polypeptide (Menkes syndrome), Copper transporting ATPase 1, Cu++ transporting P type ATPase, Menkes disease associated protein, Menkes syndrome, Menke, MC1, MC 1, MK, MNK, DSMAX, SMAX3, OHS, FLJ17790, OTTHUMP00000062077

免疫原：Synthetic peptide amino acids 42-61 (cytoplasmic C-terminus) of human Copper- transporting ATPase1

克隆性:L60/4 (Formerly sold as S60-4)

分子量:180kDa

应用稀释比例：WB (1:500), ICC/IF (1:100)

应用注释：1 µg/ml of SMC-398 was sufficient for detection of Copper-transporting ATPase1 in 20 µg of rat brain lysate by colorimetric immunoblot analysis using Goat IgG:HRP as the secondary antibody.

防腐剂:95.46mM Phosphate, 2.48mM MES and 2mM EDTA

纯化:Protein G Purified

保存说明:Conjugated antibodies should be stored according to the product label

NCBI:NP_000043.3

Entrez:538

UniProt ID:Q04656

Note:For research use only.