PEX26 Antibody Summary
| Immunogen |
Peptide with sequence C-QKPNLEGSVSHK corresponding to internal region according to NP_060399.1.
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| Epitope |
C-QKPNLEGSVSHK
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| Specificity |
Reported variants represent identical protein: NP_060399.1, NP_001121121.1
|
| Clonality |
Polyclonal
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| Host |
Goat
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| Gene |
PEX26
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| Purity |
Immunogen affinity purified
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Applications/Dilutions
| Dilutions |
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| Application Notes |
WB: Approx. 33 kDa band observed in human kidney lysates (calculated MW of 33.9 kDa band according to NP_060399.1).
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| Publications |
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Packaging, Storage & Formulations
| Storage |
Store at -20C. Avoid freeze-thaw cycles.
|
| Buffer |
0.5 mg/ml Tris (pH 7.3) and 0.5% BSA
|
| Preservative |
0.02% Sodium Azide
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| Purity |
Immunogen affinity purified
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Alternate Names for PEX26 Antibody
- FLJ20695
- peroxin-26
- peroxisomal biogenesis factor 26
- peroxisome assembly protein 26
- peroxisome biogenesis disorder, complementation group 8
- peroxisome biogenesis disorder, complementation group A
- peroxisome biogenesis factor 26
- PEX26M1T
- Pex26pM1T
Background
This gene belongs to the peroxin-26 gene family. It is probably required for protein import into peroxisomes. It anchors PEX1 and PEX6 to peroxisome membranes, possibly to form heteromeric AAA ATPase complexes required for the import of proteins into peroxisomes. Defects in this gene are the cause of peroxisome biogenesis disorder complementation group 8 (PBD-CG8). PBD refers to a group of peroxisomal disorders arising from a failure of protein import into the peroxisomal membrane or matrix. The PBD group is comprised of four disorders: Zellweger syndrome (ZWS), neonatal adrenoleukodystrophy (NALD), infantile Refsum disease (IRD), and classical rhizomelic chondrodysplasia punctata (RCDP). Two transcript variants encoding the same protein have been identified for this gene.
