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

SHOX Reaktivität: Human Wirt: Synthetic BP, WB
Produktnummer ABIN983718
  • Target Alle SHOX Produkte
    SHOX (Short Stature Homeobox (SHOX))
    Protein Region
    N-Term
    Spezies
    Human
    Quelle
    • 1
    Synthetic
    Applikation
    Blocking Peptide (BP), Western Blotting (WB)
    Produktmerkmale
    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.
    Aufreinigung
    Purified
  • Applikationshinweise
    Each Investigator should determine their own optimal working dilution for specific applications.
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Lyophilized
    Rekonstitution
    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
    Konzentration
    1 mg/mL
    Buffer
    Final peptide concentration is 1 mg/mL in PBS.
    Handhabung
    Avoid repeated freeze-thaw cycles.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Target
    SHOX (Short Stature Homeobox (SHOX))
    Synonyme
    si:ch211-134k13.1 Peptide, zgc:123182 Peptide, GCFX Peptide, PHOG Peptide, SHOXY Peptide, SS Peptide, short stature homeobox Peptide, shox Peptide, SHOX Peptide
    Hintergrund
    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
    Molekulargewicht
    32 kDa
    Gen-ID
    6473
    NCBI Accession
    NM_000451, NP_000442
    UniProt
    O15266
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