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PEX6 elisa kit :: Mouse peroxisomal biogenesis factor 6 ELISA Kit

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Catalog # MBS9322230
Unit / Price
  48-Strip-Wells  /  $470 +1 FREE 8GB USB
  96-Strip-Wells  /  $680 +1 FREE 8GB USB
  5x96-Strip-Wells  /  $3,100 +3 FREE 8GB USB
  10x96-Strip-Wells  /  $6,095 +7 FREE 8GB USB
PEX6 elisa kit
Product Name

peroxisomal biogenesis factor 6 (PEX6), ELISA Kit

Also Known As

Mouse Peroxisome assembly factor 2, PEX6 ELISA Kit

Product Synonym Names
Mouse Peroxisome assembly factor 2 (PEX6) ELISA kit; PAF-2; PAF2; PXAAA1; peroxisomal AAA-type ATPase 1; peroxisome biogenesis factor 6; peroxisomal biogenesis factor 6
Product Gene Name
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
Request for Current Manual Insert
3D Structure
ModBase 3D Structure for Q99LC9
Species Reactivity
Preparation and Storage
Store all reagents at 2-8 degree C
Product Note
Our ELISA Kit assays are dynamic research tools and sometimes they may be updated and improved. If the format of this assay is important to you then please request the current manual or contact our technical support team with a presales inquiry before placing an order. We will confirm the current details of the assay. We cannot guarantee the sample manual posted online is the most current manual.
Other Notes
Small volumes of PEX6 elisa kit vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
Searchable Terms forPEX6purchase
MBS9322230 is a ready-to-use microwell, strip plate ELISA (enzyme-linked immunosorbent assay) Kit for analyzing the presence of the peroxisomal biogenesis factor 6 (PEX6) ELISA Kit target analytes in biological samples. The concentration gradients of the kit standards or positive controls render a theoretical kit detection range in biological research samples containing PEX6. The ELISA analytical biochemical technique of the MBS9322230 kit is based on PEX6 antibody-PEX6 antigen interactions (immunosorbency) and an HRP colorimetric detection system to detect PEX6 antigen targets in samples. The ELISA Kit is designed to detect native, not recombinant, PEX6. Appropriate sample types may include undiluted body fluids and/or tissue homogenates, secretions. Quality control assays assessing reproducibility identified the intra-assay CV (%) and inter-assay CV(%).
NCBI/Uniprot data below describe general gene information for PEX6. It may not necessarily be applicable to this product.
NCBI Accession #
NCBI GenBank Nucleotide #
UniProt Primary Accession #
UniProt Secondary Accession #
UniProt Related Accession #
Molecular Weight
104,549 Da
NCBI Official Full Name
peroxisome assembly factor 2
NCBI Official Synonym Full Names
peroxisomal biogenesis factor 6
NCBI Official Symbol
NCBI Official Synonym Symbols
AI132582; mKIAA4177; D130055I09Rik
  [Similar Products]
NCBI Protein Information
peroxisome assembly factor 2; PAF-2; peroxin-6; peroxisomal-type ATPase 1
UniProt Protein Name
Peroxisome assembly factor 2
UniProt Synonym Protein Names
Peroxin-6; Peroxisomal biogenesis factor 6; Peroxisomal-type ATPase 1
Protein Family
UniProt Gene Name
UniProt Synonym Gene Names
PAF-2  [Similar Products]
UniProt Entry Name
UniProt Comments for PEX6
PEX6: Involved in peroxisome biosynthesis. Required for stability of the PTS1 receptor. Anchored by PEX26 to peroxisome membranes, possibly to form heteromeric AAA ATPase complexes required for the import of proteins into peroxisomes. Defects in PEX6 are the cause of peroxisome biogenesis disorder complementation group 4 (PBD-CG4); also known as PBD-CGC. 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 14 distinct genetic groups as concluded from complementation studies. Defects in PEX6 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. Belongs to the AAA ATPase family.

Protein type: Membrane protein, peripheral

Cellular Component: peroxisomal membrane; membrane; cytoplasm; peroxisome; cytosol

Molecular Function: protein C-terminus binding; protein binding; ATPase activity; protein complex binding; nucleotide binding; ATPase activity, coupled; ATP binding

Biological Process: protein stabilization; metabolic process; peroxisome organization and biogenesis; protein targeting to peroxisome; protein import into peroxisome matrix, translocation
All of MyBioSource's Products are for scientific laboratory research purposes and are not for diagnostic, therapeutics, prophylactic or in vivo use. Through your purchase, you expressly represent and warrant to MyBioSource that you will properly test and use any Products purchased from MyBioSource in accordance with industry standards. MyBioSource and its authorized distributors reserve the right to refuse to process any order where we reasonably believe that the intended use will fall outside of our acceptable guidelines.
While every efforts were made to ensure the accuracy of the information provided in this datasheet, MyBioSource will not be liable for any omissions or errors contained herein. MyBioSource reserves the right to make changes to this datasheet at any time without prior notice.

It is the responsibility of the customer to report product performance issues to MyBioSource within 30 days of receipt of the product. Please visit our Terms & Conditions page for more information.
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