Recombinant Human PEX1 cell lysate

• Cat.No.: PEX1-1335HCL

Specification

• Description: This gene encodes a member of the AAA ATPase family, a large group of ATPases associated with diverse cellular activities. This protein is cytoplasmic but is often anchored to a peroxisomal membrane where it forms a heteromeric complex and plays a role in the import of proteins into peroxisomes and peroxisome biogenesis. Mutations in this gene have been associated with complementation group 1 peroxisomal disorders such as neonatal adrenoleukodystrophy, infantile Refsum disease, and Zellweger syndrome.
• 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

Gene Information

• Gene Name: PEX1 peroxisomal biogenesis factor 1 [ Homo sapiens ]
• Official Symbol: PEX1
• Synonyms: PEX1; peroxisomal biogenesis factor 1; peroxisome biogenesis factor 1 , Zellweger syndrome , Zellweger syndrome 1 , ZWS, ZWS1; peroxisome biogenesis factor 1; peroxin-1; Zellweger syndrome; peroxisome biogenesis disorder protein 1; ZWS; ZWS1
• Gene ID: 5189
• mRNA Refseq: NM_000466
• Protein Refseq: NP_000457
• UniProt ID: O43933
• Chromosome Location: 7q21.2
• Pathway: Peroxisome, organism-specific biosystem; Peroxisome, conserved biosystem
• Function: ATP binding; ATP binding; ATPase activity, coupled; binding; nucleoside-triphosphatase activity; nucleotide binding; protein C-terminus binding; protein binding; protein complex binding