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USH1G Protein (His tag)

USH1G Spezies: Human Wirt: Escherichia coli (E. coli) Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Produktnummer ABIN2735083
  • Target Alle USH1G Proteine anzeigen
    USH1G (Usher Syndrome 1G (Autosomal Recessive) (USH1G))
    Protein-Typ
    Recombinant
    Spezies
    Human
    Quelle
    • 1
    Escherichia coli (E. coli)
    Aufreinigungstag / Konjugat
    Dieses USH1G Protein ist gelabelt mit His tag.
    Applikation
    Antibody Production (AbP), Standard (STD)
    Produktmerkmale
    • Recombinant human USH1G (full length, N-term HIS tag) protein expressed in E. coli.
    • Produced with end-sequenced ORF clone
    Reinheit
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product USH1G Protein
  • Applikationshinweise
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    Kommentare

    The tag is located at the N-terminal.

    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Konzentration
    50 μg/mL
    Buffer
    25 mM Tris, pH 8.0, 150 mM NaCl, 10 % glycerol, 1 % Sarkosyl.
    Lagerung
    -80 °C
    Informationen zur Lagerung
    Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
  • Target
    USH1G (Usher Syndrome 1G (Autosomal Recessive) (USH1G))
    Abstract
    USH1G Produkte
    Synonyme
    ANKS4A Protein, SANS Protein, Sans Protein, js Protein, USH1 protein network component sans Protein, USH1G Protein, Ush1g Protein
    Hintergrund
    This gene encodes a protein that contains three ankyrin domains, a class I PDZ-binding motif and a sterile alpha motif. The encoded protein interacts with harmonin, which is associated with Usher syndrome type 1C. This protein plays a role in the development and maintenance of the auditory and visual systems and functions in the cohesion of hair bundles formed by inner ear sensory cells. Mutations in this gene are associated with Usher syndrome type 1G (USH1G). Alternative splicing results in multiple transcript variants.
    Molekulargewicht
    51.3 kDa
    NCBI Accession
    NP_775748
    Pathways
    Sensory Perception of Sound
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