PEX26 Antibody

Images

 
Western Blot: PEX26 Antibody [NBP1-52048] - NBP1-52048 (0.5ug/ml) staining of Human Kidney lysate (35ug protein in RIPA buffer). Primary incubation was 1 hour. Detected by chemiluminescence.

Product Details

Summary
Reactivity HuSpecies Glossary
Applications WB, PEP-ELISA
Clonality
Polyclonal
Host
Goat
Conjugate
Unconjugated

Order Details

PEX26 Antibody Summary

Immunogen
Peptide with sequence C-QKPNLEGSVSHK corresponding to internal region according to NP_060399.1.
Epitope
C-QKPNLEGSVSHK
Specificity
Reported variants represent identical protein: NP_060399.1, NP_001121121.1
Isotype
IgG
Clonality
Polyclonal
Host
Goat
Gene
PEX26
Purity
Immunogen affinity purified
Innovator's Reward
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Applications/Dilutions

Dilutions
  • Western Blot 0.5 - 1.5 ug/ml
  • Peptide ELISA Detection limit 1:64000
Application Notes
WB: Approx. 33 kDa band observed in human kidney lysates (calculated MW of 33.9 kDa band according to NP_060399.1).
Publications
Read Publication using NBP1-52048.

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
Purity
Immunogen affinity purified

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.

Limitations

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.

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Publications for PEX26 Antibody (NBP1-52048)(1)

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Product General Protocols

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Video Protocols

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Secondary Antibodies

 

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Bioinformatics

Gene Symbol PEX26
Entrez
Uniprot