PEX26 Antibody (C-term) Blocking peptide
€363.00
In stock
SKU
AC-BP14017b
Background:
This gene belongs to the peroxin-26 gene family. It isprobably required for protein import into peroxisomes. It anchorsPEX1 and PEX6 to peroxisome membranes, possibly to form heteromericAAA ATPase complexes required for the import of proteins intoperoxisomes. Defects in this gene are the cause of peroxisomebiogenesis disorder complementation group 8 (PBD-CG8). PBD refersto a group of peroxisomal disorders arising from a failure ofprotein import into the peroxisomal membrane or matrix. The PBDgroup is comprised of four disorders: Zellweger syndrome (ZWS),neonatal adrenoleukodystrophy (NALD), infantile Refsum disease(IRD), and classical rhizomelic chondrodysplasia punctata (RCDP).Alternatively spliced transcript variants have been identified forthis gene.
Other Names:
Peroxisome assembly protein 26, Peroxin-26, PEX26
Target/Specificity:
The synthetic peptide sequence used to generate the antibody AP14017b was selected from the C-term region of PEX26. A 10 to 100 fold molar excess to antibody is recommended. Precise conditions should be optimized for a particular assay.
Gene Name: PEX26 {ECO:0000303|PubMed:12717447, ECO:0000312|HGNC:HGNC:22965}
Gene ID: 55670
Primary Accession: Q7Z412
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
This gene belongs to the peroxin-26 gene family. It isprobably required for protein import into peroxisomes. It anchorsPEX1 and PEX6 to peroxisome membranes, possibly to form heteromericAAA ATPase complexes required for the import of proteins intoperoxisomes. Defects in this gene are the cause of peroxisomebiogenesis disorder complementation group 8 (PBD-CG8). PBD refersto a group of peroxisomal disorders arising from a failure ofprotein import into the peroxisomal membrane or matrix. The PBDgroup is comprised of four disorders: Zellweger syndrome (ZWS),neonatal adrenoleukodystrophy (NALD), infantile Refsum disease(IRD), and classical rhizomelic chondrodysplasia punctata (RCDP).Alternatively spliced transcript variants have been identified forthis gene.
Other Names:
Peroxisome assembly protein 26, Peroxin-26, PEX26
Target/Specificity:
The synthetic peptide sequence used to generate the antibody AP14017b was selected from the C-term region of PEX26. A 10 to 100 fold molar excess to antibody is recommended. Precise conditions should be optimized for a particular assay.
Gene Name: PEX26 {ECO:0000303|PubMed:12717447, ECO:0000312|HGNC:HGNC:22965}
Gene ID: 55670
Primary Accession: Q7Z412
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
| Is Featured? | No |
|---|
Write Your Own Review