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ZNF259 Protein (Myc-DYKDDDDK Tag)

znf259 Origine: Humain Hôte: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
N° du produit ABIN2735974
  • Antigène Voir toutes ZNF259 (znf259) Protéines
    ZNF259 (znf259) (Zinc Finger Protein 259 (znf259))
    Type de proteíne
    Recombinant
    Origine
    • 3
    • 1
    • 1
    • 1
    • 1
    Humain
    Source
    • 4
    • 2
    • 1
    HEK-293 Cells
    Purification/Conjugué
    Cette ZNF259 protéine est marqué à la Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Attributs du produit
    • Recombinant human ZNF259 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 znf259 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
    ZNF259 (znf259) (Zinc Finger Protein 259 (znf259))
    Autre désignation
    Znf259 (znf259 Produits)
    Synonymes
    RGD1562173 Protein, zpr1 Protein, ZNF259 Protein, ZPR1 Protein, Zfp259 Protein, fc17g10 Protein, si:rp71-56i13.4 Protein, wu:fc17g10 Protein, zgc:56478 Protein, AI303781 Protein, Znf259 Protein, ZPR1 zinc finger Protein, ZPR1 zinc finger L homeolog Protein, Zpr1 Protein, ZPR1 Protein, zpr1 Protein, zpr1.L Protein
    Sujet
    The protein encoded by this gene is found in the cytoplasm of quiescent cells but translocates to the nucleolus in proliferating cells. The encoded protein interacts with survival motor neuron protein (SMN1) to enhance pre-mRNA splicing and to induce neuronal differentiation and axonal growth. Defects in this gene or the SMN1 gene can cause spinal muscular atrophy. Two transcript variants encoding different isoforms have been found for this gene.
    Poids moléculaire
    50.7 kDa
    NCBI Accession
    NP_003895
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