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Spartan antibody

C1orf124 Reactivity: Human WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN5966619
  • Target See all Spartan (C1orf124) products
    Spartan (C1orf124) (Chromosome 1 Open Reading Frame 124 (C1orf124))
    Reactivity
    • 27
    • 3
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Human
    Host
    • 26
    • 1
    Rabbit
    Clonality
    • 27
    Polyclonal
    Conjugate
    • 9
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This Spartan antibody is un-conjugated
    Application
    • 13
    • 13
    • 8
    • 6
    • 3
    • 3
    • 2
    • 1
    Western Blotting (WB)
    Purification
    Affinity purification
    Immunogen
    Recombinant protein of human SPRTN
    Isotype
    IgG
  • Application Notes
    WB 1:500 - 1:2000
    Restrictions
    For Research Use only
  • Concentration
    1 mg/mL
    Buffer
    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
    Spartan (C1orf124) (Chromosome 1 Open Reading Frame 124 (C1orf124))
    Alternative Name
    SPRTN (C1orf124 Products)
    Synonyms
    Spartan antibody, c1orf124 antibody, C1orf124 antibody, DDDL1880 antibody, DVC1 antibody, PRO4323 antibody, dJ876B10.3 antibody, C28H1orf124 antibody, SprT-like N-terminal domain antibody, sprtn antibody, SPRTN antibody
    Background

    Synonyms: C1orf124,CA124,Chromosome 1 open reading frame 124 ,DDDL1880,dJ876B10.3,PRO4323,RP5-876B10.3,Spartan,SprT-like domain at the N terminus,SprT-like N-terminal domain,Zinc finger RAD18 domain-containing protein C1orf124

    Background: The protein encoded by this gene may play a role in DNA repair during replication of damaged DNA. This protein recruits valosin containing protein (p97) to stalled DNA replication forks where it may prevent excessive translesional DNA synthesis and limit the number of DNA-damage induced mutations. It may also be involved in replication-related G2/M-checkpoint regulation. Deficiency of a similar protein in mouse causes chromosomal instability and progeroid phenotypes. Mutations in this gene have been associated with Ruijs-Aalfs syndrome (RJALS). Alternatively spliced transcript variants have been identified.

    Molecular Weight

    Observed_MW: 60kDa

    Calculated_MW: 24kDa/29kDa/55kDa

    Gene ID
    83932
    UniProt
    Q9H040
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