| Product Name | Anti-PEX26 antibody-DBCO |
|---|---|
| Antibody Type | Primary Antibodies |
| Immunogen | Polypeptide |
| Conjugation | DBCO |
| Clonality | Polyclonal |
|---|---|
| Isotype | IgG |
| Host Species | Rabbit |
| Species Reactivity | HumanMouseRat |
| Concentration | 1mg/ml |
| Purification | Protein A |
| Gene Symbol | PEX26 |
|---|---|
| Gene Synonyms | PBD7A PBD7B PEX26M1T Pex26pM1T |
| Gene Full Name | peroxisomal biogenesis factor 26 |
| Gene Summary | 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). Alternatively spliced transcript variants have been identified for this gene. [provided by RefSeq, Dec 2010] |
| Alternative Names | Em:AC008101.3 FLJ20695 peroxin-26 peroxisome biogenesis disorder complementation group 8 peroxisome biogenesis disorder complementation group A peroxisome biogenesis factor 26 |
| Molecular Weight(MW) | 33kDa（observed：35kDa) |
| Source | Rabbit |
| Cellular Localization | Peroxisome membrane |
| SwissProt ID | Q7Z412 |
|---|
| Form | Liquid |
|---|---|
| Storage Instructions | Shipped at 4°C. Store at +4°C short term (1-2 weeks). Store at -20°C long term. Avoid freeze / thaw cycle. |
| Storage Buffer | Purified antibody in PBS with 0.05% PC300,40% Glycerol. |
