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LMBRD1 Protein (Myc-DYKDDDDK Tag)

LMBRD1 Origin: Human Host: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Catalog No. ABIN2724850
  • Target See all LMBRD1 Proteins
    LMBRD1 (LMBR1 Domain Containing 1 (LMBRD1))
    Protein Type
    Recombinant
    Origin
    • 2
    • 1
    Human
    Source
    • 2
    • 1
    HEK-293 Cells
    Purification tag / Conjugate
    This LMBRD1 protein is labelled with Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Characteristics
    • Recombinant human LMBRD1 protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    Purity
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product LMBRD1 Protein
  • Application Notes
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    Comment

    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.
    Storage
    -80 °C
    Storage Comment
    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
    LMBRD1 (LMBR1 Domain Containing 1 (LMBRD1))
    Alternative Name
    Lmbrd1 (LMBRD1 Products)
    Synonyms
    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
    Background
    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].
    Molecular Weight
    61.2 kDa
    NCBI Accession
    NP_060838
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