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DFNA5 Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag)

DFNA5 Origin: Human Host: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Catalog No. ABIN2719436
  • Target See all DFNA5 Proteins
    DFNA5 (Deafness, Autosomal Dominant 5 (DFNA5))
    Protein Type
    Recombinant
    Protein Characteristics
    Transcript Variant 1
    Origin
    • 4
    • 1
    • 1
    Human
    Source
    • 2
    • 2
    • 1
    • 1
    HEK-293 Cells
    Purification tag / Conjugate
    This DFNA5 protein is labelled with Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Characteristics
    • Recombinant human DFNA5 (transcript variant 1) protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    Purity
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product DFNA5 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 C-terminal.

    Restrictions
    For Research Use only
  • Concentration
    50 μg/mL
    Buffer
    25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
    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
    DFNA5 (Deafness, Autosomal Dominant 5 (DFNA5))
    Alternative Name
    Dfna5 (DFNA5 Products)
    Synonyms
    Dfna5h Protein, fk59f08 Protein, zgc:91916 Protein, wu:fc41e05 Protein, wu:fk59f08 Protein, MGC83660 Protein, ICERE-1 Protein, 2310037D07Rik Protein, 4932441K13Rik Protein, EG14210 Protein, Fin15 Protein, gasdermin E Protein, gasdermin Eb Protein, DFNA5, deafness associated tumor suppressor Protein, gasdermin E L homeolog Protein, Gsdme Protein, gsdmeb Protein, DFNA5 Protein, gsdme.L Protein, GSDME Protein
    Background
    Hearing impairment is a heterogeneous condition with over 40 loci described. The protein encoded by this gene is expressed in fetal cochlea, however, its function is not known. Nonsyndromic hearing impairment is associated with a mutation in this gene. Three transcript variants encoding two different isoforms have been found for this gene.
    Molecular Weight
    54.4 kDa
    NCBI Accession
    NP_004394
    Pathways
    Sensory Perception of Sound
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