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PEX5 Mouse Monoclonal Antibody [Clone ID: OTI6E9]

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SKU
CF501430
Carrier-free (BSA/glycerol-free) PEX5 mouse monoclonal antibody, clone OTI6E9 (formerly 6E9)
Size:
100 ug
Formulation:
Carrier-free Standard
Conjugation:
Unconjugated
  $620.00
4 Weeks*
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View other "PEX5 or NM_000319" antibodies

Specifications
Specifications
Product Data
Clone Name OTI6E9
Application FC, IF, WB
Recommended Dilution WB 1:500~2000, IF 1:100, FLOW 1:100
Reactivity Dog, Human, Monkey, Mouse, Rat
Antibody Host Mouse
Isotype IgG1
Clonality Monoclonal
Immunogen Full length human recombinant protein of human PEX5 (NP_000310) produced in HEK293T cell.
Buffer Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)
Reconstitution Method For reconstitution, we recommend adding 100uL distilled water to a final antibody concentration of about 1 mg/mL. To use this carrier-free antibody for conjugation experiment, we strongly recommend performing another round of desalting process. (OriGene recommends Zeba Spin Desalting Columns, 7KMWCO from Thermo Scientific)
Purification Purified from mouse ascites fluids or tissue culture supernatant by affinity chromatography (protein A/G)
Conjugation Unconjugated
Storage Store at -20°C as received.
Stability Stable for 12 months from date of receipt.
Shipping Ambient
Predicted Protein Size 69.7 kDa
Gene Name peroxisomal biogenesis factor 5
Database Link
Background The product of this gene binds to the C-terminal PTS1-type tripeptide peroxisomal targeting signal (SKL-type) and plays an essential role in peroxisomal protein import. Peroxins (PEXs) are proteins that are essential for the assembly of functional peroxisomes. The peroxisome biogenesis disorders (PBDs) are a group of genetically heterogeneous autosomal recessive, lethal diseases characterized by multiple defects in peroxisome function. The peroxisomal biogenesis disorders are a heterogeneous group with at least 14 complementation groups and with more than 1 phenotype being observed in cases falling into particular complementation groups. Although the clinical features of PBD patients vary, cells from all PBD patients exhibit a defect in the import of one or more classes of peroxisomal matrix proteins into the organelle. Defects in this gene are a cause of neonatal adrenoleukodystrophy (NALD), a cause of Zellweger syndrome (ZWS) as well as may be a cause of infantile Refsum disease (IRD). Alternatively spliced transcript variants encoding different isoforms have been identified. provided by RefSeq
Synonyms PBD2A; PBD2B; PTS1-BP; PTS1R; PXR1; RCDP5
Reference Data
Protein Categories Intracellular Proteins
Protein Families Druggable Genome
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Other "OTI6E9" antibodies (4)
SKU Description Size Price
TA501430 Anti-PEX5 mouse monoclonal antibody, clone OTI6E9 (formerly 6E9) 100 ul
$447.00
TA501430AM Anti-PEX5 mouse monoclonal antibody, clone OTI6E9 (formerly 6E9), Biotinylated 100 ul
$509.00
TA501430BM Anti-PEX5 mouse monoclonal antibody, clone OTI6E9 (formerly 6E9), HRP conjugated 100 ul
$509.00
TA501430S Anti-PEX5 mouse monoclonal antibody, clone OTI6E9 (formerly 6E9) 30 ul
$200.00

file-alt Citations

Variability in intracellular localization of D-amino acid oxidase in choroid plexus epithelial cells
Ono, Shishido, Yamagishi et al
FEBS J (2026)
AI Summary: In this study, the OriGene PEX5 antibody (TA501430S) was used to investigate the colocalization of D-amino acid oxidase with peroxisomal markers in choroid plexus epithelial cells, contributing to the analysis of DAO’s subcellular localization.
Snippet: AB5A (E6N8S) Cell Signaling, 46 449 T Mouse, Monoclonal 1/1000 TSG101 [EPR7130(B)] Abcam, ab320807 Goat, Monoclonal 1/1000 PEX5 Origene, TA501430S Mouse, Monoclonal 1/1000 CD107b/LAMP2 Proteintech, 66 301-1-Ig Mouse, Monoclonal 1/1000
Showing 1-1 of 1 papers.
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