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MEGF10 Protein (His tag)

MEGF10 Origine: Humain Hôte: HEK-293 Cells Recombinant > 90 % as determined by reducing SDS-PAGE.
N° du produit ABIN7317160
  • Antigène Voir toutes MEGF10 Protéines
    MEGF10 (Multiple EGF-Like-Domains 10 (MEGF10))
    Type de proteíne
    Recombinant
    Origine
    • 3
    • 3
    Humain
    Source
    • 6
    HEK-293 Cells
    Purification/Conjugué
    Cette MEGF10 protéine est marqué à la His tag.
    Fonction
    Recombinant Human MEGF10 Protein (His Tag)
    Séquence
    Met 1-Gly857
    Attributs du produit
    A DNA sequence encoding the human MEGF10 (NP_115822.1) (Met1-Gly857) was expressed with a polyhistidine tag at the C-terminus.
    Pureté
    > 90 % as determined by reducing SDS-PAGE.
    niveau d'endotoxine
    < 1.0 EU per μg of the protein as determined by the LAL method.
    Top Product
    Discover our top product MEGF10 Protéine
  • Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    Please refer to the printed manual for detailed information.
    Buffer
    Lyophilized from sterile PBS, pH 7.4
    Stock
    4 °C,-20 °C,-80 °C
    Stockage commentaire
    Generally, lyophilized proteins are stable for up to 12 months when stored at -20 to -80°C. Reconstituted protein solution can be stored at 4-8°C for 2-7 days. Aliquots of reconstituted samples are stable at < -20°C for 3 months.
  • Antigène
    MEGF10 (Multiple EGF-Like-Domains 10 (MEGF10))
    Autre désignation
    MEGF10 (MEGF10 Produits)
    Synonymes
    EMARDD Protein, 3000002B06Rik Protein, Gm331 Protein, multiple EGF-like domains 10 Protein, multiple EGF like domains 10 Protein, multiple EGF-like-domains 10 Protein, Megf10 Protein, MEGF10 Protein
    Sujet

    Background: This gene encodes a member of the multiple epidermal growth factor-like domains protein family. The encoded protein plays a role in cell adhesion, motility and proliferation, and is a critical mediator of apoptotic cell phagocytosis as well as amyloid-beta peptide uptake in the brain. Expression of this gene may be associated with schizophrenia, and mutations in this gene are a cause of early-onset myopathy, areflexia, respiratory distress, and dysphagia (EMARDD) as well as congenital myopathy with minicores. Alternatively spliced transcript variants have been observed for this gene.

    Synonym: EMARDD

    Poids moléculaire
    90.2 kDa
    NCBI Accession
    NP_115822
    Pathways
    Regulation of Muscle Cell Differentiation
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