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LMBRD1 Protein (Myc-DYKDDDDK Tag)

LMBRD1 Origine: Humain Hôte: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
N° du produit ABIN2724850
  • Antigène Voir toutes LMBRD1 Protéines
    LMBRD1 (LMBR1 Domain Containing 1 (LMBRD1))
    Type de proteíne
    Recombinant
    Origine
    • 2
    • 1
    Humain
    Source
    • 2
    • 1
    HEK-293 Cells
    Purification/Conjugué
    Cette LMBRD1 protéine est marqué à la Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Attributs du produit
    • Recombinant human LMBRD1 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 LMBRD1 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
    LMBRD1 (LMBR1 Domain Containing 1 (LMBRD1))
    Autre désignation
    Lmbrd1 (LMBRD1 Produits)
    Synonymes
    fc08a03 Protein, wu:fc08a03 Protein, zgc:103471 Protein, MGC89794 Protein, C6orf209 Protein, LMBD1 Protein, MAHCF Protein, NESI Protein, 0910001K20Rik Protein, AV347960 Protein, LMBR1 domain containing 1 Protein, LMBR1 domain containing 1 L homeolog Protein, lmbrd1 Protein, LMBRD1 Protein, MCYG_07794 Protein, Lmbrd1 Protein, lmbrd1.L Protein
    Sujet
    This gene encodes a lysosomal membrane protein that may be involved in the transport and metabolism of cobalamin. This protein also interacts with the large form of the hepatitis delta antigen and may be required for the nucleocytoplasmic shuttling of the hepatitis delta virus. Mutations in this gene are associated with the vitamin B12 metabolism disorder termed, homocystinuria-megaloblastic anemia complementation type F.[provided by RefSeq, Oct 2009].
    Poids moléculaire
    61.2 kDa
    NCBI Accession
    NP_060838
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