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PEX6 Antibody
PEX6 Antibody, Clone S233-8
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
Application 
| WB, ICC/IF |
|---|---|
| Primary Accession | Q13608 |
| Other Accession | NP_000278.3 |
| Host | Mouse |
| Isotype | IgG1 |
| Reactivity | Human, Rat |
| Clonality | Monoclonal |
| Description | Mouse Anti-Human PEX6 Monoclonal IgG1 |
| Target/Specificity | Detects ~100kDa. |
| Other Names | PAF 2 Antibody, Peroxin 6 Antibody, Peroxisomal AAA type ATPase 1 Antibody, Peroxisomal biogenesis factor 6 Antibody, PXAAA1 Antibody, peroxisomal-type ATPase 1 Antibody, peroxisome biogenesis factor 6 Antibody |
| Clone Names | S233-8 |
| Immunogen | Fusion protein amino acids 2-294 (N-terminus) of human PEX6. Rat: 82% identity (243/293 amino acids identical). Mouse: 82% identity (244/294 amino acids identical). <50% identity with other PEX proteins. |
| Purification | Protein G Purified |
| Storage | -20ºC |
| Storage Buffer | PBS pH 7.4, 50% glycerol, 0.1% sodium azide |
| Shipping Temperature | Blue Ice or 4ºC |
| Certificate of Analysis | 1 µg/ml of SMC-470 was sufficient for detection of PEX6 in 20 µg of rat brain lysate by colorimetric immunoblot analysis using Goat anti-mouse IgG:HRP as the secondary antibody. |
| Cellular Localization | Cytoplasm | Peroxisome | Peroxisome Membrane |
Thousands of laboratories across the world have published research that depended on the performance of antibodies from Abcepta to advance their research. Check out links to articles that cite our products in major peer-reviewed journals, organized by research category.
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Provided below are standard protocols that you may find useful for product applications.
Background
This gene encodes a member of the AAA (ATPases associated with diverse cellular activities) family of ATPases. This member is a predominantly cytoplasmic protein, which plays a direct role in peroxisomal protein import and is required for PTS1 (peroxisomal targeting signal 1, a C-terminal tripeptide of the sequence ser-lys-leu) receptor activity. Mutations in this gene cause peroxisome biogenesis disorders of complementation group 4 and complementation group 6.
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