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TMEM67 anticorps (C-Term)

TMEM67 Reactivité: Humain WB Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN5517188
  • Antigène Voir toutes TMEM67 Anticorps
    TMEM67 (Transmembrane Protein 67 (TMEM67))
    Épitope
    • 5
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    C-Term
    Reactivité
    • 19
    • 3
    • 1
    Humain
    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)
    Séquence
    FDLLFFCVVD LACQNFILAS FLTYLQQEIF RYIRNTVGQK NLASKTLVDQ
    Purification
    Affinity purified
    Immunogène
    The immunogen is a synthetic peptide directed towards the C terminal region of human TMEM67
    Top Product
    Discover our top product TMEM67 Anticorps primaire
  • Indications d'application
    Optimal working dilution should be determined by the investigator.
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
    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
    For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent 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).

    Alias Symbols: MKS3, JBTS6, NPHP11, TNEM67, MECKELIN,

    Protein Size: 995
    ID gène
    91147
    NCBI Accession
    NM_001142301, NP_001135773
    UniProt
    Q5HYA8
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