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PLAGL1 Protein (His tag)

PLAGL1 Origine: Humain Hôte: Escherichia coli (E. coli) Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
N° du produit ABIN2729110
  • Antigène Voir toutes PLAGL1 Protéines
    PLAGL1 (Pleiomorphic Adenoma Gene-Like 1 (PLAGL1))
    Type de proteíne
    Recombinant
    Origine
    • 4
    • 1
    Humain
    Source
    • 2
    • 1
    • 1
    • 1
    Escherichia coli (E. coli)
    Purification/Conjugué
    Cette PLAGL1 protéine est marqué à la His tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Attributs du produit
    • Recombinant human PLAGL1 (full length, N-term HIS tag, transcript variant 7) protein expressed in E.coli.
    • Produced with end-sequenced ORF clone
    Pureté
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product PLAGL1 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 N-terminal.

    Restrictions
    For Research Use only
  • Concentration
    50 μg/mL
    Buffer
    50 mM Tris, pH 8.0, 500 mM NaCl, 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
    PLAGL1 (Pleiomorphic Adenoma Gene-Like 1 (PLAGL1))
    Autre désignation
    Plagl1 (PLAGL1 Produits)
    Synonymes
    PLAGL1 Protein, LOT1 Protein, ZAC Protein, ZAC1 Protein, Lot1 Protein, Zac1 Protein, PLAG1 like zinc finger 1 Protein, uncharacterized LOC100350914 Protein, pleiomorphic adenoma gene-like 1 Protein, PLAGL1 Protein, LOC100350914 Protein, Plagl1 Protein
    Sujet
    This gene encodes a C2H2 zinc finger protein that functions as a suppressor of cell growth. This gene is often deleted or methylated and silenced in cancer cells. In addition, overexpression of this gene during fetal development is thought to be the causal factor for transient neonatal diabetes mellitus (TNDM). Alternative splicing and the use of alternative promoters results in multiple transcript variants encoding two different protein isoforms. The P1 downstream promoter of this gene is imprinted, with preferential expression from the paternal allele in many tissues.
    Poids moléculaire
    44.5 kDa
    NCBI Accession
    NP_001074424
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