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ST7 antibody (AA 268-309)

ST7 Reactivity: Human WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN5708171
  • Target See all ST7 Antibodies
    ST7 (Suppression of Tumorigenicity 7 (ST7))
    Binding Specificity
    • 9
    • 7
    • 7
    • 6
    • 2
    • 1
    • 1
    AA 268-309
    Reactivity
    • 21
    • 3
    • 3
    Human
    Host
    • 21
    • 1
    Rabbit
    Clonality
    • 22
    Polyclonal
    Conjugate
    • 12
    • 2
    • 2
    • 2
    • 2
    • 2
    This ST7 antibody is un-conjugated
    Application
    • 21
    • 16
    • 14
    • 3
    • 1
    • 1
    Western Blotting (WB)
    Purification
    Antigen affinity purified
    Immunogen
    Amino acids 268-309 (DGCYRRSQQLQHHGSQYEAQHRRDTNVLVYIKRRLAMCARRL-human) were used as the immunogen for the ST7 antibody.
    Isotype
    IgG
    Top Product
    Discover our top product ST7 Primary Antibody
  • Application Notes
    Optimal dilution of the ST7 antibody should be determined by the researcher.\. Western blot: 0.5-1 μg/mL
    Restrictions
    For Research Use only
  • Buffer
    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water
    Storage
    -20 °C
    Storage Comment
    After reconstitution, the ST7 antibody can be stored for up to one month at 4°C. For long-term, aliquot and store at -20°C. Avoid repeated freezing and thawing.
  • Target
    ST7 (Suppression of Tumorigenicity 7 (ST7))
    Alternative Name
    Suppressor of Tumorigenicity 7 (ST7 Products)
    Synonyms
    ETS7q antibody, FAM4A antibody, FAM4A1 antibody, HELG antibody, RAY1 antibody, SEN4 antibody, TSG7 antibody, 9430001H04Rik antibody, Fam4a2 antibody, suppression of tumorigenicity 7 antibody, ST7 antibody, St7 antibody
    Background
    Suppressor of tumorigenicity protein 7 is a protein that in humans is encoded by the ST7 gene. The gene for this product maps to a region on chromosome 7 identified as an autism-susceptibility locus. Mutation screening of the entire coding region in autistic individuals failed to identify phenotype-specific variants, suggesting that coding mutations for this gene are unlikely to be involved in the etiology of autism. The function of this gene product has not been determined. Transcript variants encoding different isoforms of this protein have been described.
    UniProt
    Q9NRC1
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