PEX26 Antibody

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.

This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.

We have publications tested in 1 confirmed species: Human.

We have publications tested in 3 applications: ICC/IF, IF/IHC, WB.

Showing Publications 1 - 2 of 2.

Publications using NBP1-32743	Applications	Species
Dahabieh MS, Huang F, Goncalves C et al. Silencing PEX26 as an unconventional mode to kill drug-resistant cancer cells and forestall drug resistance Autophagy 2021-06-21 [PMID: 34074205] (IF/IHC)	IF/IHC
Law KB, Bronte-Tinkew D, Di Pietro E et al. The peroxisomal AAA ATPase complex prevents pexophagy and development of peroxisome biogenesis disorders Autophagy. 2017-05-04 [PMID: 28521612] (WB, ICC/IF, Human) Details: Citation used the HRP format of this antibody.	WB, ICC/IF	Human

Array NBP1-32743

• PEX26 Antibodies
• PEX26 Lysates
• PEX26 Protein