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CCL17 anticorps (AA 101-200) (Alexa Fluor 350)

CCL17 Reactivité: Souris WB, IF (cc), IF (p) Hôte: Lapin Polyclonal Alexa Fluor 350
N° du produit ABIN6976421
  • Antigène Voir toutes CCL17 Anticorps
    CCL17 (Chemokine (C-C Motif) Ligand 17 (CCL17))
    Épitope
    • 15
    • 14
    • 12
    • 10
    • 8
    • 7
    • 6
    • 6
    • 6
    • 5
    • 5
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 101-200
    Reactivité
    • 71
    • 46
    • 10
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    Souris
    Hôte
    • 105
    • 6
    • 3
    • 1
    Lapin
    Clonalité
    • 108
    • 7
    Polyclonal
    Conjugué
    • 44
    • 20
    • 11
    • 7
    • 3
    • 3
    • 3
    • 3
    • 3
    • 3
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    Cet anticorp CCL17 est conjugé à/à la Alexa Fluor 350
    Application
    • 79
    • 57
    • 25
    • 25
    • 23
    • 9
    • 8
    • 6
    • 6
    • 4
    • 4
    • 4
    • 3
    • 2
    • 2
    • 2
    Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
     Réactivité croisée
    Souris
    Homologie
    Human,Rat,Dog,Cow,Sheep,Pig,Horse
    Purification
    Purified by Protein A.
    Immunogène
    KLH conjugated synthetic peptide derived from human ABCD2
    Isotype
    IgG
    Top Product
    Discover our top product CCL17 Anticorps primaire
  • Indications d'application
    IF(IHC-P) 1:50-200
    IF(IHC-F) 1:50-200
    IF(ICC) 1:50-200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 μg/μL
    Buffer
    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
    Agent conservateur
    ProClin
    Précaution d'utilisation
    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
    Stock
    -20 °C
    Stockage commentaire
    Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
    Date de péremption
    12 months
  • Antigène
    CCL17 (Chemokine (C-C Motif) Ligand 17 (CCL17))
    Autre désignation
    ABCD2 (CCL17 Produits)
    Synonymes
    anticorps A-152E5.3, anticorps ABCD-2, anticorps SCYA17, anticorps TARC, anticorps CCL17, anticorps Abcd-2, anticorps Scya17, anticorps Scya17l, anticorps Tarc, anticorps abcd2, anticorps C-C motif chemokine ligand 17, anticorps chemokine (C-C motif) ligand 17, anticorps ATP-binding cassette sub-family D member 2, anticorps CCL17, anticorps Ccl17, anticorps LOC100537809
    Sujet

    Synonyms: ABC39, Abcd2, ABCD2_HUMAN, Adrenoleukodystrophy-like 1, Adrenoleukodystrophy-related protein, ALDL1, ALDR, ALDRP, ATP-binding cassette sub-family D member 2, hALDR.

    Background: 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]

    ID gène
    225
    UniProt
    Q9UBJ2
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