ABCD1 polyclonal antibody (A01)

Catalog # H00000215-A01

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Size:50 uL
Price: USD $ 243.00
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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QC Test

Western Blot detection against Immunogen (37.11 KDa) .

  • Specification

    Product Description

    Mouse polyclonal antibody raised against a partial recombinant ABCD1.

    Immunogen

    ABCD1 (AAH15541, 1 a.a. ~ 100 a.a) partial recombinant protein with GST tag.

    Sequence

    MPVLSRPRPWRGNTLKRTAVLLALAAYGAHKVYPLVRQCLAPARGLQAPAGEPTQEASGVAAAKAGMNRVFLQRLLWLLRLLFPRVLCRETGLLALHSAA

    Host

    Mouse

    Reactivity

    Human

    Interspecies Antigen Sequence

    Mouse (85); Rat (82)

    Quality Control Testing

    Antibody Reactive Against Recombinant Protein.

    Western Blot detection against Immunogen (37.11 KDa) .

    Storage Buffer

    50 % glycerol

    Storage Instruction

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

  • Applications

    Western Blot (Recombinant protein)

    ELISA

  • Gene Info — ABCD1

    Entrez GeneID

    215

    GeneBank Accession#

    BC015541

    Protein Accession#

    AAH15541

    Gene Name

    ABCD1

    Gene Alias

    ABC42, ALD, ALDP, AMN

    Gene Description

    ATP-binding cassette, sub-family D (ALD), member 1

    Omim ID

    300100 300371

    Gene Ontology

    Hyperlink

    Gene Summary

    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 is likely involved in the peroxisomal transport or catabolism of very long chain fatty acids. Defects in this gene have been identified as the underlying cause of adrenoleukodystrophy, an X-chromosome recessively inherited demyelinating disorder of the nervous system. [provided by RefSeq

    Other Designations

    OTTHUMP00000025960|adrenoleukodystrophy protein

  • Interactome
  • Pathway
  • Disease
Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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