PEX26 Antibody

Novus Biologicals | Catalog # NBP1-52048

Novus Biologicals
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Key Product Details

Species Reactivity

Human

Applications

Western Blot, Peptide ELISA

Label

Unconjugated

Antibody Source

Polyclonal Goat IgG
View all PEX26 Primary Antibodies »

Product Specifications

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

Clonality

Polyclonal

Host

Goat

Isotype

IgG

Scientific Data Images for PEX26 Antibody

Western Blot: PEX26 Antibody [NBP1-52048]

Western Blot: PEX26 Antibody [NBP1-52048]

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.

Applications for PEX26 Antibody

Application
Recommended Usage

Peptide ELISA

Detection limit 1:64000

Western Blot

0.5 - 1.5 ug/ml
Application Notes
WB: Approx. 33 kDa band observed in human kidney lysates (calculated MW of 33.9 kDa band according to NP_060399.1).

Formulation, Preparation, and Storage

Purification

Immunogen affinity purified

Formulation

Tris saline (20 mM Tris pH 7.3, 150 mM NaCl), 0.5% BSA

Preservative

0.02% Sodium Azide

Concentration

0.5 mg/ml

Shipping

The product is shipped with polar packs. Upon receipt, store it immediately at the temperature recommended below.

Stability & Storage

Store at -20C. Avoid freeze-thaw cycles.

Background: PEX26

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.

Alternate Names

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

Entrez Gene IDs

55670 (Human)

Gene Symbol

PEX26

UniProt

NP_060399.1 (Human)

Additional PEX26 Products

Product Documents for PEX26 Antibody

Certificate of Analysis

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Product Specific Notices for PEX26 Antibody

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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