Phone:
+1 877 302 8632
Fax:
+1 888 205 9894 (Toll-free)
E-Mail:
orders@antibodies-online.com

USH1G Protein (His tag)

USH1G Origin: Human Host: Escherichia coli (E. coli) Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Catalog No. ABIN2735083
  • Target See all USH1G Proteins
    USH1G (Usher Syndrome 1G (Autosomal Recessive) (USH1G))
    Protein Type
    Recombinant
    Origin
    Human
    Source
    • 1
    Escherichia coli (E. coli)
    Purification tag / Conjugate
    This USH1G protein is labelled with His tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Characteristics
    • Recombinant human USH1G (full length, N-term HIS tag) protein expressed in E. coli.
    • Produced with end-sequenced ORF clone
    Purity
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product USH1G Protein
  • Application Notes
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    Comment

    The tag is located at the N-terminal.

    Restrictions
    For Research Use only
  • Concentration
    50 μg/mL
    Buffer
    25 mM Tris, pH 8.0, 150 mM NaCl, 10 % glycerol, 1 % Sarkosyl.
    Storage
    -80 °C
    Storage Comment
    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 Products
    Synonyms
    ANKS4A Protein, SANS Protein, Sans Protein, js Protein, USH1 protein network component sans Protein, USH1G Protein, Ush1g Protein
    Background
    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.
    Molecular Weight
    51.3 kDa
    NCBI Accession
    NP_775748
    Pathways
    Sensory Perception of Sound
You are here:
Support