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FAM136A Protein (Myc-DYKDDDDK Tag)

FAM136A Origine: Humain Hôte: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
N° du produit ABIN2720753
  • Antigène Voir toutes FAM136A Protéines
    FAM136A (Family with Sequence Similarity 136, Member A (FAM136A))
    Type de proteíne
    Recombinant
    Origine
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Humain
    Source
    • 5
    • 2
    HEK-293 Cells
    Purification/Conjugué
    Cette FAM136A protéine est marqué à la Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Attributs du produit
    • Recombinant human FAM136A protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    Pureté
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product FAM136A Protéine
  • Indications d'application
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    Commentaires

    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.
    Stock
    -80 °C
    Stockage commentaire
    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.
  • Antigène
    FAM136A (Family with Sequence Similarity 136, Member A (FAM136A))
    Autre désignation
    Fam136a (FAM136A Produits)
    Synonymes
    2010309E21Rik Protein, AW124904 Protein, Hyccin Protein, RGD1304825 Protein, ik:tdsubc_1a11 Protein, wu:fb72f05 Protein, xx:tdsubc_1a11 Protein, zgc:73247 Protein, family with sequence similarity 136 member A Protein, family with sequence similarity 136, member A Protein, family with sequence similarity 136 member A S homeolog Protein, FAM136A Protein, Fam136a Protein, fam136a.S Protein, fam136a Protein
    Sujet
    This gene encodes a mitochondrially localized protein that is highly conserved across species. The gene is expressed in a variety of tissues including human lymphoblast cells and rat neurosensorial epithelium of the cristaampullaris. A mutation in this gene has been associated with familial Meniere's disease, a chronic disorder of the inner ear. Several pseudogenes of this gene are found on other chromosomes. Alternative splicing results in multiple transcript variants.
    Poids moléculaire
    15.5 kDa
    NCBI Accession
    NP_116211
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