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TMEM67 anticorps

TMEM67 Reactivité: Souris, Rat WB Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN6293383
  • Antigène Voir toutes TMEM67 Anticorps
    TMEM67 (Transmembrane Protein 67 (TMEM67))
    Reactivité
    Souris, Rat
    Hôte
    • 20
    Lapin
    Clonalité
    • 20
    Polyclonal
    Conjugué
    • 10
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp TMEM67 est non-conjugé
    Application
    • 8
    • 6
    • 4
    • 2
    Western Blotting (WB)
    Purification
    Affinity purification
    Immunogène
    Recombinant protein of human TMEM67
    Isotype
    IgG
    Top Product
    Discover our top product TMEM67 Anticorps primaire
  • Indications d'application
    WB 1:200 - 1:2000
    Commentaires

    Widely expressed in adult and fetal tissues, Expressed at higher level in spinal cord

    Restrictions
    For Research Use only
  • Buffer
    PBS with 0.02 % sodium azide, 50 % glycerol,  pH 7.3.
    Agent conservateur
    Sodium azide
    Précaution d'utilisation
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Stock
    -20 °C
    Stockage commentaire
    Store at -20C. Avoid freeze / thaw cycles.
  • Antigène
    TMEM67 (Transmembrane Protein 67 (TMEM67))
    Autre désignation
    TMEM67 (TMEM67 Produits)
    Synonymes
    anticorps JBTS6, anticorps MECKELIN, anticorps MKS3, anticorps NPHP11, anticorps TNEM67, anticorps 5330408M12Rik, anticorps B230117O07, anticorps b2b1163.1Clo, anticorps b2b1291.1Clo, anticorps Wpk, anticorps transmembrane protein 67, anticorps TMEM67, anticorps tmem67, anticorps Tmem67
    Sujet
    The protein encoded by this gene localizes to the primary cilium and to the plasma membrane. The gene functions in centriole migration to the apical membrane and formation of the primary cilium. Multiple transcript variants encoding different isoforms have been found for this gene. Defects in this gene are a cause of Meckel syndrome type 3 (MKS3) and Joubert syndrome type 6 (JBTS6).
    Poids moléculaire
    111.745 kDa
    ID gène
    91147
    UniProt
    Q5HYA8
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