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TMEM67 anticorps (Isoform 1)

TMEM67 Reactivité: Humain WB Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN1886737
  • Antigène Voir toutes TMEM67 Anticorps
    TMEM67 (Transmembrane Protein 67 (TMEM67))
    Épitope
    • 5
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Isoform 1
    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)
    Purification
    Purified by antigen-affinity chromatography.
    Immunogène
    Recombinant protein fragment contain a sequence corresponding to a region within amino acids 231 and 480 of Human TMEM67
    Top Product
    Discover our top product TMEM67 Anticorps primaire
  • Indications d'application
    Suggested dilutions:
    Western blotting: 1.500-1.3000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    0.1 M Tris-buffered saline with 10 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.
    Agent conservateur
    Thimerosal (Merthiolate)
    Précaution d'utilisation
    Biohazard Informations: This product contains thimerosal which is hazardous.
    Stock
    4 °C/-20 °C
    Stockage commentaire
    Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.
  • Antigène
    TMEM67 (Transmembrane Protein 67 (TMEM67))
    Autre désignation
    meckelin (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).[provided by RefSeq]
    Poids moléculaire
    112 kDa
    ID gène
    91147
    NCBI Accession
    NP_714915, NM_153704
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