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TMEM67 Antikörper (Isoform 1)

TMEM67 Reaktivität: Human WB Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN1886737
  • Target Alle TMEM67 Antikörper anzeigen
    TMEM67 (Transmembrane Protein 67 (TMEM67))
    Bindungsspezifität
    • 5
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Isoform 1
    Reaktivität
    • 19
    • 3
    • 1
    Human
    Wirt
    • 20
    Kaninchen
    Klonalität
    • 20
    Polyklonal
    Konjugat
    • 10
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser TMEM67 Antikörper ist unkonjugiert
    Applikation
    • 8
    • 6
    • 4
    • 2
    Western Blotting (WB)
    Aufreinigung
    Purified by antigen-affinity chromatography.
    Immunogen
    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 Primärantikörper
  • Applikationshinweise
    Suggested dilutions:
    Western blotting: 1.500-1.3000
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Buffer
    0.1 M Tris-buffered saline with 10 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.
    Konservierungsmittel
    Thimerosal (Merthiolate)
    Vorsichtsmaßnahmen
    Biohazard Informations: This product contains thimerosal which is hazardous.
    Lagerung
    4 °C/-20 °C
    Informationen zur Lagerung
    Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.
  • Target
    TMEM67 (Transmembrane Protein 67 (TMEM67))
    Andere Bezeichnung
    meckelin (TMEM67 Produkte)
    Synonyme
    JBTS6 antikoerper, MECKELIN antikoerper, MKS3 antikoerper, NPHP11 antikoerper, TNEM67 antikoerper, 5330408M12Rik antikoerper, B230117O07 antikoerper, b2b1163.1Clo antikoerper, b2b1291.1Clo antikoerper, Wpk antikoerper, transmembrane protein 67 antikoerper, TMEM67 antikoerper, tmem67 antikoerper, Tmem67 antikoerper
    Hintergrund
    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]
    Molekulargewicht
    112 kDa
    Gen-ID
    91147
    NCBI Accession
    NP_714915, NM_153704
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