PEX7 DNAxPab

Catalog # H00005191-W01P

Size

Price

Stock

Quantity

Size:200 ug
Price: USD $ 620.00
Stock:
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
  • Specifications

    Product Description

    Rabbit polyclonal antibody raised against a partial-length human PEX7 DNA using DNAx™ Immune technology.DNAx Polyclonal Antibody,DNAx Polyclonal Antibodies,DNAx Pab,DNAx Polyclonal,DNA Immune,DNA Immunization,Immune Technology,Hard-to-Find Antibody,Hard-to-Find Antibodies,Hard-to-Find,Hard to Find,HardtoFind

    Technology

    DNAx™ Immune

    Immunogen

    Extracellular membrane domain (ECD) human DNA

    Host

    Rabbit

    Reactivity

    Human

    Purification

    Protein A

    Quality Control Testing

    Antibody reactive against mammalian transfected lysate.

    Storage Buffer

    In 1x PBS, pH 7.4

    Storage Instruction

    Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.

  • Applications

    Western Blot (Transfected lysate)

    Immunofluorescence (Transfected cell)

    Flow Cytometry (Transfected cell)

  • Gene Info — PEX7

    Entrez GeneID

    5191

    GeneBank Accession#

    NM_000288.1

    Protein Accession#

    NP_000279.1

    Gene Name

    PEX7

    Gene Alias

    PTS2R, RCDP1, RD

    Gene Description

    peroxisomal biogenesis factor 7

    Omim ID

    215100 266500 601757

    Gene Ontology

    Hyperlink

    Gene Summary

    This gene encodes the cytosolic receptor for the set of peroxisomal matrix enzymes targeted to the organelle by the peroxisome targeting signal 2 (PTS2). Defects in this gene cause peroxisome biogenesis disorders (PBDs), which are characterized by multiple defects in peroxisome function. There are at least 14 complementation groups for PBDs, with more than one 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 have been associated with PBD complementation group 11 (PBD-CG11) disorders, rhizomelic chondrodysplasia punctata type 1 (RCDP1), and Refsum disease (RD). [provided by RefSeq

    Other Designations

    OTTHUMP00000017277|peroxin-7|peroxisomal PTS2 receptor|peroxisome targeting signal 2 receptor

  • Interactomes
  • Diseases
Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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