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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
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$591.60
$696.00
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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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