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Human peroxisomal biogenesis factor 26 ELISA Kit | PEX26 elisa kit

Human Peroxisome assembly protein 26, PEX26 ELISA Kit

Gene Names
PEX26; PBD7A; PBD7B; PEX26M1T; Pex26pM1T
Reactivity
Human
Synonyms
peroxisomal biogenesis factor 26; Human Peroxisome assembly protein 26; PEX26 ELISA Kit; Human Peroxisome assembly protein 26 (PEX26) ELISA kit; FLJ20695; PEX26M1T; Pex26pM1T; peroxin-26; peroxisome assembly protein 26; peroxisome biogenesis disorder; complementation group 8; complementation group A; peroxisome bi; PEX26 elisa kit
Ordering
For Research Use Only!
Reactivity
Human
Preparation and Storage
Store all reagents at 2-8 degree C

NCBI and Uniprot Product Information

NCBI GI #
NCBI GeneID
NCBI Accession #
NCBI GenBank Nucleotide #
UniProt Accession #
Molecular Weight
33,898 Da
NCBI Official Full Name
peroxisome assembly protein 26 isoform a
NCBI Official Synonym Full Names
peroxisomal biogenesis factor 26
NCBI Official Symbol
PEX26
NCBI Official Synonym Symbols
PBD7A; PBD7B; PEX26M1T; Pex26pM1T
NCBI Protein Information
peroxisome assembly protein 26; peroxin-26; peroxisome biogenesis factor 26; peroxisome biogenesis disorder, complementation group 8; peroxisome biogenesis disorder, complementation group A
UniProt Protein Name
Peroxisome assembly protein 26
UniProt Gene Name
PEX26
UniProt Entry Name
PEX26_HUMAN

NCBI Description

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]

Uniprot Description

PEX26: Probably required for protein import into peroxisomes. Anchors PEX1 and PEX6 to peroxisome membranes, possibly to form heteromeric AAA ATPase complexes required for the import of proteins into peroxisomes. Involved in the import of catalase and proteins containing a PTS2 target sequence, but not in import of proteins with a PTS1 target sequence. Defects in PEX26 are the cause of peroxisome biogenesis disorder complementation group 8 (PBD-CG8); also known as PBD-CGA. 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). ZWS, NALD and IRD are distinct from RCDP and constitute a clinical continuum of overlapping phenotypes known as the Zellweger spectrum. The PBD group is genetically heterogeneous with at least 13 distinct genetic groups as concluded from complementation studies. Defects in PEX26 are a cause of Zellweger syndrome (ZWS). ZWS is a fatal peroxisome biogenesis disorder characterized by dysmorphic facial features, hepatomegaly, ocular abnormalities, renal cysts, hearing impairment, profound psychomotor retardation, severe hypotonia and neonatal seizures. Death occurs within the first year of life. Defects in PEX26 are a cause of adrenoleukodystrophy neonatal (NALD). NALD is a peroxisome biogenesis disorder characterized by the accumulation of very long-chain fatty acids, adrenal insufficiency and mental retardation. Defects in PEX26 are a cause of infantile Refsum disease (IRD). IRD is a mild peroxisome biogenesis disorder. Clinical features include early onset, mental retardation, minor facial dysmorphism, retinopathy, sensorineural hearing deficit, hepatomegaly, osteoporosis, failure to thrive, and hypocholesterolemia. The biochemical abnormalities include accumulation of phytanic acid, very long chain fatty acids (VLCFA), di- and trihydroxycholestanoic acid and pipecolic acid. Belongs to the peroxin-26 family.

Protein type: Membrane protein, integral

Chromosomal Location of Human Ortholog: 22q11.21

Cellular Component: integral to peroxisomal membrane; peroxisome

Molecular Function: protein C-terminus binding; protein binding; protein complex binding; ATPase binding

Biological Process: protein import into peroxisome matrix; protein import into peroxisome membrane

Disease: Peroxisome Biogenesis Disorder 7b; Peroxisome Biogenesis Disorder 7a (zellweger)

Research Articles on PEX26

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Product Notes

The Human PEX26 pex26 (Catalog #AAA9332602) is an ELISA Kit and is intended for research purposes only. The product is available for immediate purchase. The AAA9332602 ELISA Kit recognizes Human PEX26. It is sometimes possible for the material contained within the vial of "peroxisomal biogenesis factor 26, ELISA Kit" to become dispersed throughout the inside of the vial, particularly around the seal of said vial, during shipment and storage. We always suggest centrifuging these vials to consolidate all of the liquid away from the lid and to the bottom of the vial prior to opening. Please be advised that certain products may require dry ice for shipping and that, if this is the case, an additional dry ice fee may also be required.

Precautions

All products in the AAA Biotech catalog are strictly for research-use only, and are absolutely not suitable for use in any sort of medical, therapeutic, prophylactic, in-vivo, or diagnostic capacity. By purchasing a product from AAA Biotech, you are explicitly certifying that said products will be properly tested and used in line with industry standard. AAA Biotech and its authorized distribution partners reserve the right to refuse to fulfill any order if we have any indication that a purchaser may be intending to use a product outside of our accepted criteria.

Disclaimer

Though we do strive to guarantee the information represented in this datasheet, AAA Biotech cannot be held responsible for any oversights or imprecisions. AAA Biotech reserves the right to adjust any aspect of this datasheet at any time and without notice. It is the responsibility of the customer to inform AAA Biotech of any product performance issues observed or experienced within 30 days of receipt of said product. To see additional details on this or any of our other policies, please see our Terms & Conditions page.

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