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Shugoshin antibody

This anti-Shugoshin antibody is a Rabbit Polyclonal antibody detecting Shugoshin in IF. Suitable for Human, Mouse and Rat.
Catalog No. ABIN7258968

Quick Overview for Shugoshin antibody (ABIN7258968)

Target

See all Shugoshin (SGOL1) Antibodies
Shugoshin (SGOL1) (Shugoshin 1 (SGOL1))

Reactivity

  • 38
  • 4
  • 4
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

  • 37
  • 3
Rabbit

Clonality

  • 38
  • 2
Polyclonal

Conjugate

  • 25
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Shugoshin antibody is un-conjugated

Application

  • 26
  • 22
  • 5
  • 4
  • 2
  • 2
  • 1
  • 1
Immunofluorescence (IF)
  • Characteristics

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogen

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

    Isotype

    IgG
  • Application Notes

    IF 1:50-1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

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

    Preservative

    Sodium azide

    Precaution of Use

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

    Storage

    -20 °C

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    Shugoshin (SGOL1) (Shugoshin 1 (SGOL1))

    Alternative Name

    SGOL1

    Background

    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.

    Gene ID

    151648

    UniProt

    Q5FBB7

    Pathways

    Maintenance of Protein Location
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