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Short Stature Homeobox (SHOX) (N-Term) Peptide

SHOX Reactivity: Human Host: Synthetic BP, WB
Catalog No. ABIN983718
  • Target See all SHOX products
    SHOX (Short Stature Homeobox (SHOX))
    Protein Region
    N-Term
    Origin
    Human
    Source
    • 1
    Synthetic
    Application
    Blocking Peptide (BP), Western Blotting (WB)
    Characteristics
    This is a synthetic peptide designed for use in combination with anti-SHOX antibody (Catalog #: ARP33284_P050). It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
    Purification
    Purified
  • Application Notes
    Each Investigator should determine their own optimal working dilution for specific applications.
    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
    Concentration
    1 mg/mL
    Buffer
    Final peptide concentration is 1 mg/mL in PBS.
    Handling Advice
    Avoid repeated freeze-thaw cycles.
    Storage
    -20 °C
    Storage Comment
    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Target
    SHOX (Short Stature Homeobox (SHOX))
    Synonyms
    si:ch211-134k13.1 Peptide, zgc:123182 Peptide, GCFX Peptide, PHOG Peptide, SHOXY Peptide, SS Peptide, short stature homeobox Peptide, shox Peptide, SHOX Peptide
    Background
    This gene belongs to the paired homeobox family and is located in the pseudoautosomal region 1 (PAR1) of X and Y chromosomes. Defects in this gene are associated with idiopathic growth retardation and in the short stature phenotype of Turner syndrome patients. This gene is highly conserved across species from mammals to fish to flies.This gene belongs to the paired homeobox family and is located in the pseudoautosomal region 1 (PAR1) of X and Y chromosomes. Defects in this gene are associated with idiopathic growth retardation and in the short stature phenotype of Turner syndrome patients. This gene is highly conserved across species from mammals to fish to flies. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene.

    Alias Symbols: GCFX, PHOG, SHOXY, SS

    Protein Interaction Partner: CSNK2A1

    Protein Size: 292
    Molecular Weight
    32 kDa
    Gene ID
    6473
    NCBI Accession
    NM_000451, NP_000442
    UniProt
    O15266
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