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>   home   >   Products   >   Primary Antibodies   >   Signal Transduction   >   PEX6 Antibody (monoclonal) (M04)   

PEX6 Antibody (monoclonal) (M04)

Mouse monoclonal antibody raised against a partial recombinant PEX6.

  • WB - PEX6 Antibody (monoclonal) (M04) AT3272a
    Antibody Reactive Against Recombinant Protein.Western Blot detection against Immunogen (36.74 KDa) .
  • WB - PEX6 Antibody (monoclonal) (M04) AT3272a
    PEX6 monoclonal antibody (M04), clone 3G3. Western Blot analysis of PEX6 expression in K-562 ( (Cat # AT3272a )
  • E - PEX6 Antibody (monoclonal) (M04) AT3272a
    Detection limit for recombinant GST tagged PEX6 is approximately 0.3ng/ml as a capture antibody.
Product Information
  • Applications Legend:
  • WB=Western Blot
  • IHC=Immunohistochemistry
  • IHC-P=Immunohistochemistry (Paraffin-embedded Sections)
  • IHC-F=Immunohistochemistry (Frozen Sections)
  • IF=Immunofluorescence
  • FC=Flow Cytopmetry
  • IC=Immunochemistry
  • ICC=Immunocytochemistry
  • IP=Immunoprecipitation
  • DB=Dot Blot
  • CHIP=Chromatin Immunoprecipitation
  • FA=Fluorescence Assay
  • IEM=Immunoelectronmicroscopy
  • EIA=Enzyme Immunoassay
Primary Accession Q13608
Other Accession NM_000287
Reactivity Human
Host mouse
Clonality Monoclonal
Isotype IgG2a Kappa
Clone Names 3G3
Calculated MW 104061 Da
Additional Information
Gene ID 5190
Other Names Peroxisome assembly factor 2, PAF-2, Peroxin-6, Peroxisomal biogenesis factor 6, Peroxisomal-type ATPase 1, PEX6, PXAAA1
Target/Specificity PEX6 (NP_000278, 881 a.a. ~ 980 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.
Dilution WB~~1:500~1000
Format Clear, colorless solution in phosphate buffered saline, pH 7.2 .
StorageStore at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
PrecautionsPEX6 Antibody (monoclonal) (M04) is for research use only and not for use in diagnostic or therapeutic procedures.
Research Areas
Citations (0)

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This gene encodes a member of the AAA (ATPases associated with diverse cellular activities) family of ATPases. This member is a predominantly cytoplasmic protein, which plays a direct role in peroxisomal protein import and is required for PTS1 (peroxisomal targeting signal 1, a C-terminal tripeptide of the sequence ser-lys-leu) receptor activity. Mutations in this gene cause peroxisome biogenesis disorders of complementation group 4 and complementation group 6.


Spectrum of PEX6 mutations in Zellweger syndrome spectrum patients. Ebberink MS, et al. Hum Mutat, 2010 Jan. PMID 19877282.Maternally inherited Leigh syndrome: T8993G mutation in a Tunisian family. Mkaouar-Rebai E, et al. Pediatr Neurol, 2009 Jun. PMID 19433277.Identification of novel mutations and sequence variation in the Zellweger syndrome spectrum of peroxisome biogenesis disorders. Yik WY, et al. Hum Mutat, 2009 Mar. PMID 19105186.Dynamic and functional assembly of the AAA peroxins, Pex1p and Pex6p, and their membrane receptor Pex26p. Tamura S, et al. J Biol Chem, 2006 Sep 22. PMID 16854980.Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes. Kimura K, et al. Genome Res, 2006 Jan. PMID 16344560.

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$ 315.00
Cat# AT3272a
(40 western blots)
Availability: 7-10 days
Bulk Size
Seasonal Special on Bulk Order
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