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WB analysis of HepG2 (A), MCF7 (B), SH-SY5Y (C), SP2/0 (D), PC12 (E) whole cell lysates using GTX54937 PMP70 antibody.
WB analysis of HepG2 (A), MCF7 (B), SH-SY5Y (C), SP2/0 (D), PC12 (E) whole cell lysates using GTX54937 PMP70 antibody.
WB analysis of HepG2 (A), MCF7 (B), SH-SY5Y (C), SP2/0 (D), PC12 (E) whole cell lysates using GTX54937 PMP70 antibody.

PMP70 antibody

GTX54937
GeneTex
ApplicationsWestern Blot
Product group Antibodies
ReactivityHuman, Mouse, Rat
TargetABCD3
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Overview

  • Supplier
    GeneTex
  • Product Name
    PMP70 antibody
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 1:500 - 1:1000. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Western Blot
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Conjugate
    Unconjugated
  • Gene ID5825
  • Target name
    ABCD3
  • Target description
    ATP binding cassette subfamily D member 3
  • Target synonyms
    70 kDa peroxisomal membrane protein; ABC43; ATP-binding cassette sub-family D member 3; ATP-binding cassette, sub-family D (ALD), member 3; CBAS5; dJ824O18.1 (ATP-binding cassette, sub-family D (ALD), member 3 (PMP70, PXMP1)); peroxisomal membrane protein 1 (70kD, Zellweger syndrome); peroxisomal membrane protein 70 kDa; Peroxisomal membrane protein-1 (70kD); PMP70; PXMP1; ZWS2
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDP28288
  • Protein Name
    ATP-binding cassette sub-family D member 3
  • Scientific Description
    The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the ALD subfamily, which is involved in peroxisomal import of fatty acids and/or fatty acyl-CoAs in the organelle. All known peroxisomal ABC transporters are half transporters which require a partner half transporter molecule to form a functional homodimeric or heterodimeric transporter. This peroxisomal membrane protein likely plays an important role in peroxisome biogenesis. Mutations have been associated with some forms of Zellweger syndrome, a heterogeneous group of peroxisome assembly disorders. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2008]
  • Reactivity
    Human, Mouse, Rat
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203