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Invitrogen™ PEX1 Polyclonal Antibody, Invitrogen™
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. Alternatively spliced transcript variants have been found for this gene.
Specifications
Specifications
| Antigen | PEX1 |
| Applications | Immunohistochemistry (Paraffin), Western Blot |
| Classification | Polyclonal |
| Concentration | 0.5 mg/mL |
| Conjugate | Unconjugated |
| Formulation | PBS with 50% glycerol and 0.05% Proclin 300; pH 7.4 |
| Gene | Pex1 |
| Gene Accession No. | O43933, Q5BL07 |
| Gene Alias | 5430414H02Rik; E330005K07Rik; HMLR1; PBD1A; PBD1B; Peroxin-1; peroxisomal biogenesis factor 1; peroxisome biogenesis disorder protein 1; Peroxisome biogenesis factor 1; Pex1; RGD1559939; Zellweger syndrome; ZWS; ZWS1 |
| Gene Symbols | Pex1 |
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