Telefon:
+49 (0)241 95 163 153
Fax:
+49 (0)241 95 163 155
E-Mail:
orders@antikoerper-online.de

TMEM67 Antikörper (C-Term)

Dieses Anti-TMEM67-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von TMEM67 in WB. Geeignet für Human.
Produktnummer ABIN5517188

Kurzübersicht für TMEM67 Antikörper (C-Term) (ABIN5517188)

Target

Alle TMEM67 Antikörper anzeigen
TMEM67 (Transmembrane Protein 67 (TMEM67))

Reaktivität

  • 20
  • 4
  • 2
Human

Wirt

  • 21
Kaninchen

Klonalität

  • 20
  • 1
Polyklonal

Konjugat

  • 11
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser TMEM67 Antikörper ist unkonjugiert

Applikation

  • 9
  • 6
  • 5
  • 3
  • 1
  • 1
Western Blotting (WB)
  • Bindungsspezifität

    • 5
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    C-Term

    Sequenz

    FDLLFFCVVD LACQNFILAS FLTYLQQEIF RYIRNTVGQK NLASKTLVDQ

    Aufreinigung

    Affinity purified

    Immunogen

    The immunogen is a synthetic peptide directed towards the C terminal region of human TMEM67
  • Applikationshinweise

    Optimal working dilution should be determined by the investigator.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Buffer

    Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

    Konservierungsmittel

    Sodium azide

    Vorsichtsmaßnahmen

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Lagerung

    -20 °C

    Informationen zur Lagerung

    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.
  • Target

    TMEM67 (Transmembrane Protein 67 (TMEM67))

    Andere Bezeichnung

    TMEM67

    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).

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

    Protein Size: 995

    Gen-ID

    91147

    NCBI Accession

    NM_001142301, NP_001135773

    UniProt

    Q5HYA8
Sie sind hier:
Chat with us!