This website uses cookies to ensure you get the best experience on our website.
- Table of Contents
Designing an IHC experiment for PEX1? The guide has the expected staining pattern, antigen retrieval and fixation, antibodies backed by real IHC images, the tissue controls to run alongside, and protocols taken from published papers.
Open the PEX1 IHC GuideFacts about Peroxisome biogenesis factor 1.
.
| Human | |
|---|---|
| Gene Name: | PEX1 |
| Uniprot: | O43933 |
| Entrez: | 5189 |

| Belongs to: |
|---|
| AAA ATPase family |

peroxin-1; peroxisomal biogenesis factor 1; Peroxisome biogenesis disorder protein 1; peroxisome biogenesis factor 1; Zellweger syndrome 1; Zellweger syndrome; ZWS; ZWS1
Mass (kDA):
142.867 kDA

| Human | |
|---|---|
| Location: | 7q21.2 |
| Sequence: | 7; NC_000007.14 (92487023..92528520, complement) |
Cytoplasm. Peroxisome membrane. Associated with peroxisomal membranes.





PMID: 9398848 by Portsteffen H., et al. Human PEX1 is mutated in complementation group 1 of the peroxisome biogenesis disorders.
PMID: 9398847 by Reuber B.E., et al. Mutations in PEX1 are the most common cause of peroxisome biogenesis disorders.