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Chemokine (C-C Motif) Ligand 17 (CCL17) (N-Term) Peptide

CCL17 Reactivity: Human Host: Synthetic BP, WB
Catalog No. ABIN8096850
$145.08
Plus shipping costs $50.00
100 μg
Shipping to: United States
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Quick Overview for Chemokine (C-C Motif) Ligand 17 (CCL17) (N-Term) Peptide (ABIN8096850)

Target

CCL17 (Chemokine (C-C Motif) Ligand 17 (CCL17))

Origin

Human

Source

  • 5
Synthetic

Application

Blocking Peptide (BP), Western Blotting (WB)
  • Protein Region

    N-Term

    Purpose

    ABCD2 Peptide - N-terminal region

    Sequence

    FIIKLIKWLM IAIPATFVNS AIRYLECKLA LAFRTRLVDH AYETYFTNQT
  • Application Notes

    Optimal working dilution should be determined by the investigator.

    Comment

    This is a synthetic peptide designed for use in combination with anti-ABCD2 Antibody(ARP43657_P050),. It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications. Please inquire for more details.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Add 100 µL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.

    Buffer

    Lyophilized powder

    Storage

    -20 °C

    Storage Comment

    For longer periods of storage, store at -20 °C. Avoid repeat freeze-thaw cycles.
  • Target

    CCL17 (Chemokine (C-C Motif) Ligand 17 (CCL17))

    Background

    Background Information: 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.

    Alternative Symbols: ABC39, ALDL1, ALDR, ALDRP, hALDR

    Molecular Weight

    83kDa

    Gene ID

    225

    NCBI Accession

    NP_005155

    UniProt

    Q9UBJ2
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