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IFITM5 Antikörper (PE-Cy5)

This anti-IFITM5 antibody (ABIN1712946) is a Rabbit Polyclonal antibody detecting IFITM5 in WB. Suitable for Human.
Produktnummer ABIN1712946

Kurzübersicht für IFITM5 Antikörper (PE-Cy5) (ABIN1712946)

Target

Alle IFITM5 Antikörper anzeigen
IFITM5 (Interferon Induced Transmembrane Protein 5 (IFITM5))

Reaktivität

  • 19
  • 10
  • 2
  • 2
  • 1
  • 1
  • 1
Human

Wirt

  • 19
Kaninchen

Klonalität

  • 19
Polyklonal

Konjugat

  • 7
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Dieser IFITM5 Antikörper ist konjugiert mit PE-Cy5

Applikation

  • 14
  • 10
  • 1
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Homologie

    Human

    Aufreinigung

    Purified by Protein A.

    Immunogen

    KLH conjugated synthetic peptide derived from human IFITM5

    Isotyp

    IgG
  • Applikationshinweise

    FCM(1:100-500)
    Optimal working dilution should be determined by the investigator.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Konzentration

    1 μg/μL

    Buffer

    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

    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

    Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

    Haltbarkeit

    12 months
  • Target

    IFITM5 (Interferon Induced Transmembrane Protein 5 (IFITM5))

    Andere Bezeichnung

    IFITM5

    Hintergrund

    Synonyms: Bone-restricted interferon-induced transmembrane protein-like protein, BRIL, Fragilis4, Hrmp1, ITM5, M5_HUMAN, Interferon-induced transmembrane protein 5.

    Background: IFITM5 is a membrane protein thought to play a role in bone mineralization. This gene is located on chromosome 11 in a cluster of related genes which are induced by interferon, however, this gene has not been shown to be interferon inducible. A similar gene, located in a gene cluster on mouse chromosome 7, is a member of the interferon-inducible fragilis gene family. The mouse gene encodes a transmembrane protein described as participating in germ cell competence. A mutation in the 5' UTR of this gene has been associated with osteogenesis imperfecta type V (PMID: 22863190, 22863195).

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