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Invitrogen™ PEX1 Polyclonal Antibody
Rabbit Polyclonal Antibody
Supplier: Invitrogen™ PA5100677
Description
Antibody detects endogenous levels of total PEX1.
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
PEX1 | |
Polyclonal | |
Unconjugated | |
Pex1 | |
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 | |
Rabbit | |
Affinity chromatography | |
RUO | |
5189, 71382 | |
-20°C | |
Liquid |
Immunohistochemistry (Paraffin), Western Blot | |
1 mg/mL | |
PBS with 50% glycerol and 0.02% sodium azide; pH 7.4 | |
O43933, Q5BL07 | |
Pex1 | |
A synthesized peptide derived from human PEX1(Accession O43933), corresponding to amino acid residues L176-Y196. | |
100 μL | |
Primary | |
Human, Mouse | |
Antibody | |
IgG |
Safety and Handling
WARNING: Cancer - www.P65Warnings.ca.gov
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