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Peroxin 1 Polyclonal Antibody

Polyclonal antibody

Specification

BYab-04065

  • 50UL $180 100UL $255
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Host
Reactiveness
Use
Molecular weight (DA)
Immunogen
The antiserum was produced against synthesized peptide derived from human PEX1. AA range:1234-1283
Specificity
Peroxin 1 Polyclonal Antibody detects endogenous levels of Peroxin 1 protein.
Source
Formulation
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Dilution rate
IHC: 1/100 - 1/300. ELISA: 1/10000.. IF 1:50-200
Purification process (Immunogen)
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration
1 mg/ml
Background
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. [provided by RefSeq, Sep 2013],
Function
disease:Defects in PEX1 are a cause of adrenoleukodystrophy neonatal (NALD) [MIM:202370]. NALD is a peroxisome biogenesis disorder (PBD) characterized by the accumulation of very long-chain fatty acids, adrenal insufficiency and mental retardation.,disease:Defects in PEX1 are a cause of infantile Refsum disease (IRD) [MIM:266510]. IRD is a mild peroxisome biogenesis disorder (PBD). Clinical features include early onset, mental retardation, minor facial dysmorphism, retinopathy, sensorineural hearing deficit, hepatomegaly, osteoporosis, failure to thrive, and hypocholesterolemia. The biochemical abnormalities include accumulation of phytanic acid, very long chain fatty acids (VLCFA), di- and trihydroxycholestanoic acid and pipecolic acid.,disease:Defects in PEX1 are the cause of peroxisome biogenesis disorder complementation group 1 (PBD-CG1) [MIM:602136]; also known as PBD-CGE. PBD refer
Gene Name
PEX1
Protein name
Peroxisome biogenesis factor 1
Abbreviation
Peroxin 1
Other name
PEX1; Peroxisome biogenesis factor 1; Peroxin-1; Peroxisome biogenesis disorder protein 1
Fields
>>Peroxisome
Human gene ID
5189
Human protein sequence Database
O43933
Mouse gene ID
71382
Mouse protein sequence database
Q5BL07
Rat gene ID
Rat protein sequence database
Cellular localization
Cytoplasm. Peroxisome membrane. Associated with peroxisomal membranes.
Tissue expression
Brain,Lymph,Trachea,
Storage
-20°C/1 year

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Peroxin 1 Polyclonal Antibody

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