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Shugoshin Antikörper

Dieses Anti-Shugoshin-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von Shugoshin in IF. Geeignet für Human, Maus und Ratte.
Produktnummer ABIN7258968

Kurzübersicht für Shugoshin Antikörper (ABIN7258968)

Target

Alle Shugoshin (SGOL1) Antikörper anzeigen
Shugoshin (SGOL1) (Shugoshin 1 (SGOL1))

Reaktivität

  • 39
  • 4
  • 4
  • 1
  • 1
  • 1
Human, Maus, Ratte

Wirt

  • 38
  • 3
Kaninchen

Klonalität

  • 39
  • 2
Polyklonal

Konjugat

  • 26
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser Shugoshin Antikörper ist unkonjugiert

Applikation

  • 27
  • 23
  • 6
  • 4
  • 2
  • 2
  • 1
  • 1
Immunofluorescence (IF)
  • Produktmerkmale

    Polyclonal Antibody

    Aufreinigung

    Affinity purification

    Immunogen

    Recombinant fusion protein of human SGOL1 (NP_612493.1).

    Isotyp

    IgG
  • Applikationshinweise

    IF 1:50-1:200

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Konzentration

    1 mg/mL

    Buffer

    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3

    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. Avoid freeze / thaw cycles.
  • Target

    Shugoshin (SGOL1) (Shugoshin 1 (SGOL1))

    Andere Bezeichnung

    SGOL1

    Hintergrund

    The protein encoded by this gene is a member of the shugoshin family of proteins. This protein is thought to protect centromeric cohesin from cleavage during mitotic prophase by preventing phosphorylation of a cohesin subunit. Reduced expression of this gene leads to the premature loss of centromeric cohesion, mis-segregation of sister chromatids, and mitotic arrest. Evidence suggests that this protein also protects a small subset of cohesin found along the length of the chromosome arms during mitotic prophase. An isoform lacking exon 6 has been shown to play a role in the cohesion of centrioles (PMID: 16582621 and PMID:18331714). Mutations in this gene have been associated with Chronic Atrial and Intestinal Dysrhythmia (CAID) syndrome, characterized by the co-occurrence of Sick Sinus Syndrome (SSS) and Chronic Intestinal Pseudo-obstruction (CIPO) within the first four decades of life (PMID:25282101). Fibroblast cells from CAID patients exhibited both increased cell proliferation and higher rates of senescence. Pseudogenes of this gene have been found on chromosomes 1 and 7. Alternative splicing results in multiple transcript variants.

    Gen-ID

    151648

    UniProt

    Q5FBB7

    Pathways

    Maintenance of Protein Location
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