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anti-PEX12 antibody :: PEX12 Antibody

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Catalog # MBS8518749
Unit / Price
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  0.1 mg  /  $290 +1 FREE 8GB USB
Western Blot (WB)
Product Name

PEX12, Antibody

Full Product Name

PEX12 Antibody

Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
OMIM
266510
3D Structure
ModBase 3D Structure for O00623
Other Notes
Small volumes of anti-PEX12 antibody 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.

Western Blot (WB) of anti-PEX12 antibody
Western blot analysis PEX12 using LOVO whole cell lysates
anti-PEX12 antibody Western Blot (WB) (WB) image
NCBI/Uniprot data below describe general gene information for PEX12. It may not necessarily be applicable to this product.
NCBI GI #
NCBI GeneID
NCBI Accession #
NCBI GenBank Nucleotide #
UniProt Primary Accession #
UniProt Secondary Accession #
UniProt Related Accession #
Molecular Weight
40,797 Da
NCBI Official Full Name
peroxisome assembly protein 12
NCBI Official Synonym Full Names
peroxisomal biogenesis factor 12
NCBI Official Symbol
PEX12  [Similar Products]
NCBI Official Synonym Symbols
PAF-3; PBD3A
  [Similar Products]
NCBI Protein Information
peroxisome assembly protein 12
UniProt Protein Name
Peroxisome assembly protein 12
UniProt Synonym Protein Names
Peroxin-12; Peroxisome assembly factor 3; PAF-3
UniProt Gene Name
PEX12  [Similar Products]
UniProt Synonym Gene Names
PAF3; PAF-3  [Similar Products]
NCBI Summary for PEX12
This gene belongs to the peroxin-12 family. 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 Zellweger syndrome (ZWS). [provided by RefSeq, Oct 2008]
UniProt Comments for PEX12
Required for protein import into peroxisomes.
Precautions
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.
Disclaimer
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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