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Anti-ABCD2 Rabbit Polyclonal Antibody
Anti-ABCD2 Rabbit Polyclonal Antibody
Catalog #: 77436-992
Supplier:  Bioss
New Product
Anti-ABCD2 Rabbit Polyclonal Antibody
Catalog #: 77436-992
Supplier:  Bioss
New Product
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Specifications

  • Antibody type:
    Primary
  • Antigen name:
    ABCD2
  • Clonality:
    Polyclonal
  • Gene ID:
    225
  • Host:
    Rabbit
  • Isotype:
    IgG (H, L)
  • Reactivity:
    Mouse
  • Conjugation:
    Unconjugated
  • ELISA:
    Yes
  • Flow cytometry:
    Yes
  • ImmunoChemistry:
    Yes
  • ImmunoFluorescence:
    Yes
  • Size:
    100 µl
  • Western blot:
    Yes
  • Storage buffer:
    0.01 M TBS (pH 7.4) with 1% BSA, 0.02% Proclin300 and 50% glycerol
  • Molecular weight:
    83
  • Storage temperature:
    Shipped at 4 ℃. Store at −20 °C for one year. Avoid repeated freeze/thaw cycles.
  • Concentration:
    1 µg/µl
  • Purification:
    Purified by protein A
  • Packaging:
    Vial

Specifications

About this item

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. The function of this peroxisomal membrane protein is unknown; however this protein is speculated to function as a dimerization partner of ABCD1 and/or other peroxisomal ABC transporters. Mutations in this gene have been observed in patients with adrenoleukodystrophy, a severe demyelinating disease. This gene has been identified as a candidate for a modifier gene, accounting for the extreme variation among adrenoleukodystrophy phenotypes. This gene is also a candidate for a complement group of Zellweger syndrome, a genetically heterogeneous disorder of peroxisomal biogenesis. [provided by RefSeq, Jul 2008]

Type: Primary
Antigen: ABCD2
Clonality: Polyclonal
Clone:
Conjugation: Unconjugated
Epitope:
Host: Rabbit
Isotype: IgG (H, L)
Reactivity: Mouse

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