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PHF6 Protein (His tag)

PHF6 Spezies: Human Wirt: Escherichia coli (E. coli) Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Produktnummer ABIN2728823
  • Target Alle PHF6 Proteine anzeigen
    PHF6 (PHD Finger Protein 6 (PHF6))
    Protein-Typ
    Recombinant
    Spezies
    • 4
    • 1
    • 1
    Human
    Quelle
    • 2
    • 2
    • 1
    • 1
    Escherichia coli (E. coli)
    Aufreinigungstag / Konjugat
    Dieses PHF6 Protein ist gelabelt mit His tag.
    Applikation
    Antibody Production (AbP), Standard (STD)
    Produktmerkmale
    • Recombinant human PHF6 (full length, N-term HIS tag, transcript variant 3) protein expressed in E.coli.
    • Produced with end-sequenced ORF clone
    Reinheit
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product PHF6 Protein
  • Applikationshinweise
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    Kommentare

    The tag is located at the N-terminal.

    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Konzentration
    50 μg/mL
    Buffer
    25 mM Tris, pH 8.0, 150 mM NaCl, 10 % glycerol, 1 % Sarkosyl.
    Lagerung
    -80 °C
    Informationen zur Lagerung
    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
    PHF6 (PHD Finger Protein 6 (PHF6))
    Andere Bezeichnung
    Phf6 (PHF6 Produkte)
    Synonyme
    zgc:55403 Protein, wu:fa22g03 Protein, BFLS Protein, BORJ Protein, CENP-31 Protein, 2700007B13Rik Protein, 4931428F02Rik Protein, mKIAA1823 Protein, PHD finger protein 6 Protein, PHD finger protein 6 L homeolog Protein, phf6 Protein, phf6.L Protein, PHF6 Protein, Phf6 Protein
    Hintergrund
    This gene is a member of the plant homeodomain (PHD)-like finger (PHF) family. It encodes a protein with two PHD-type zinc finger domains, indicating a potential role in transcriptional regulation, that localizes to the nucleolus. Mutations affecting the coding region of this gene or the splicing of the transcript have been associated with Borjeson-Forssman-Lehmann syndrome (BFLS), a disorder characterized by mental retardation, epilepsy, hypogonadism, hypometabolism, obesity, swelling of subcutaneous tissue of the face, narrow palpebral fissures, and large ears. Alternate splicing results in multiple transcript variants, encoding different isoforms.
    Molekulargewicht
    35.1 kDa
    NCBI Accession
    NP_115711
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