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Shugoshin Antikörper

Dieser 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

  • 36
  • 4
  • 4
  • 1
  • 1
  • 1
Human, Maus, Ratte

Wirt

  • 35
  • 3
Kaninchen

Klonalität

  • 36
  • 2
Polyklonal

Konjugat

  • 23
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser Shugoshin Antikörper ist unkonjugiert

Applikation

  • 25
  • 20
  • 5
  • 4
  • 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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