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TMEM231 Protein (Transcript Variant 3) (Myc-DYKDDDDK Tag)

TMEM231 Origine: Humain Hôte: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
N° du produit ABIN2723165
  • Antigène Voir toutes TMEM231 Protéines
    TMEM231 (Transmembrane Protein 231 (TMEM231))
    Type de proteíne
    Recombinant
    Attributs du protein
    Transcript Variant 3
    Origine
    • 2
    • 1
    Humain
    Source
    • 2
    • 1
    HEK-293 Cells
    Purification/Conjugué
    Cette TMEM231 protéine est marqué à la Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Attributs du produit
    • Recombinant human Hypothetical protein FLJ22167 (FLJ22167), transcript variant 3 (transcript variant 3) 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 TMEM231 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
    TMEM231 (Transmembrane Protein 231 (TMEM231))
    Autre désignation
    Hypothetical Protein Flj22167 (Flj22167) (TMEM231 Produits)
    Synonymes
    zgc:64166 Protein, ALYE870 Protein, JBTS20 Protein, PRO1886 Protein, 4932417I16Rik Protein, Gm178 Protein, RGD1306153 Protein, transmembrane protein 231 Protein, tmem231 Protein, TMEM231 Protein, Tmem231 Protein
    Sujet
    This gene encodes a transmembrane protein, which is a component of the B9 complex involved in the formation of the diffusion barrier between the cilia and plasma membrane. Mutations in this gene cause Joubert syndrome (JBTS). Multiple alternatively spliced transcript variants have been found for this gene.
    Poids moléculaire
    22.7 kDa
    NCBI Accession
    NP_001070887
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