Recombinant Human SNX15 cell lysate

• Cat.No.: SNX15-1660HCL

Specification

• Description: This gene encodes a member of the sorting nexin family. Members of this family contain a phox (PX) domain, which is a phosphoinositide binding domain, and are involved in intracellular trafficking. Overexpression of this gene results in a decrease in the processing of insulin and hepatocyte growth factor receptors to their mature subunits. This decrease is caused by the mislocalization of furin, the endoprotease responsible for cleavage of insulin and hepatocyte growth factor receptors. This protein is involved in endosomal trafficking from the plasma membrane to recycling endosomes or the trans-Golgi network. This gene encodes two transcript variants encoding distinct isoforms.
• Species: Human
• Size: 100 ul
• Storage Buffer: 1X Sample Buffer (50 mM Tris-HCl, 2% SDS, 10% glycerol, 300 mM 2-mercaptoethanol, 0.01% Bromophenol blue)
• Applications: Western Blot
• Tag: Non

Gene Information

• Gene Name: SNX15 sorting nexin 15 [ Homo sapiens ]
• Official Symbol: SNX15
• Synonyms: SNX15; sorting nexin 15; sorting nexin-15; clone iota unknown protein; HSAF001435
• Gene ID: 29907
• mRNA Refseq: NM_013306
• Protein Refseq: NP_037438
• MIM: 605964
• UniProt ID: Q9NRS6
• Chromosome Location: 11q12
• Pathway: PDGFR-beta signaling pathway, organism-specific biosystem
• Function: lipid binding; phosphatidylinositol binding; protein transporter activity