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SHOX2 antibody

SHOX2 Reactivity: Human, Rat, Mouse WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7264337
  • Target See all SHOX2 Antibodies
    SHOX2 (Short Stature Homeobox 2 (SHOX2))
    Reactivity
    • 17
    • 9
    • 7
    • 5
    • 5
    • 5
    • 4
    • 3
    • 2
    • 2
    • 2
    Human, Rat, Mouse
    Host
    • 10
    • 7
    Rabbit
    Clonality
    • 13
    • 4
    Polyclonal
    Conjugate
    • 17
    This SHOX2 antibody is un-conjugated
    Application
    • 14
    • 8
    • 2
    • 1
    • 1
    Western Blotting (WB)
    Characteristics
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogen
    Recombinant fusion protein of human SHOX2 (NP_003021.3).
    Isotype
    IgG
    Top Product
    Discover our top product SHOX2 Primary Antibody
  • Application Notes
    WB 1:500-1:2000
    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
    SHOX2 (Short Stature Homeobox 2 (SHOX2))
    Alternative Name
    SHOX2 (SHOX2 Products)
    Synonyms
    SHOX2 antibody, og12 antibody, shot antibody, og12x antibody, ogi2x antibody, OG12 antibody, OG12X antibody, SHOT antibody, 6330543G17Rik antibody, Og12x antibody, Prx3 antibody, zgc:65884 antibody, zgc:77344 antibody, short stature homeobox 2 antibody, SHOX2 antibody, shox2 antibody, Shox2 antibody
    Background
    This gene is a member of the homeobox family of genes that encode proteins containing a 60-amino acid residue motif that represents a DNA binding domain. Homeobox genes have been characterized extensively as transcriptional regulators involved in pattern formation in both invertebrate and vertebrate species. Several human genetic disorders are caused by aberrations in human homeobox genes. This locus represents a pseudoautosomal homeobox gene that is thought to be responsible for idiopathic short stature, and it is implicated in the short stature phenotype of Turner syndrome patients. This gene is considered to be a candidate gene for Cornelia de Lange syndrome. Alternative splicing results in multiple transcript variants.
    Molecular Weight

    Observed_MW: 30 kDa

    Calculated_MW: 33 kDa/34 kDa/37 kDa

    Gene ID
    6474
    UniProt
    O60902
    Pathways
    Regulation of Muscle Cell Differentiation, Skeletal Muscle Fiber Development
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