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CFHR3 Protein (Transcript Variant 2) (Myc-DYKDDDDK Tag)

CFHR3 Origine: Humain Hôte: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
N° du produit ABIN2712459
  • Antigène Voir toutes CFHR3 Protéines
    CFHR3 (Complement Factor H-Related 3 (CFHR3))
    Type de proteíne
    Recombinant
    Attributs du protein
    Transcript Variant 2
    Origine
    Humain
    Source
    • 3
    • 2
    • 1
    HEK-293 Cells
    Purification/Conjugué
    Cette CFHR3 protéine est marqué à la Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Attributs du produit
    • Recombinant human Complement factor H-related 3 (CFHR3), transcript variant 2. (transcript variant 2) 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 CFHR3 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
    CFHR3 (Complement Factor H-Related 3 (CFHR3))
    Abstract
    CFHR3 Produits
    Synonymes
    EG624286 Protein, CFHL3 Protein, DOWN16 Protein, FHR-3 Protein, FHR3 Protein, HLF4 Protein, complement factor H-related 3 Protein, complement factor H related 3 Protein, Cfhr3 Protein, CFHR3 Protein
    Sujet
    The protein encoded by this gene is a secreted protein, which belongs to the complement factor H-related protein family. It binds to heparin, and may be involved in complement regulation. Mutations in this gene are associated with decreased risk of age-related macular degeneration, and with an increased risk of atypical hemolytic-uremic syndrome. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
    Poids moléculaire
    31.2
    NCBI Accession
    NP_001160096
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