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MEGF10 antibody

MEGF10 Reactivity: Human, Mouse, Rat IF Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7255341
  • Target See all MEGF10 Antibodies
    MEGF10 (Multiple EGF-Like-Domains 10 (MEGF10))
    Reactivity
    Human, Mouse, Rat
    Host
    • 24
    Rabbit
    Clonality
    • 24
    Polyclonal
    Conjugate
    • 5
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This MEGF10 antibody is un-conjugated
    Application
    • 13
    • 13
    • 7
    • 5
    • 3
    • 3
    • 1
    • 1
    • 1
    Immunofluorescence (IF)
    Characteristics
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogen
    Recombinant fusion protein of human MEGF10 (NP_001295048.1).
    Isotype
    IgG
  • Application Notes
    IF 1:50-1:200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 mg/mL
    Buffer
    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    MEGF10 (Multiple EGF-Like-Domains 10 (MEGF10))
    Alternative Name
    MEGF10 (MEGF10 Products)
    Synonyms
    EMARDD antibody, 3000002B06Rik antibody, Gm331 antibody, multiple EGF-like domains 10 antibody, multiple EGF like domains 10 antibody, multiple EGF-like-domains 10 antibody, Megf10 antibody, MEGF10 antibody
    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.
    Gene ID
    84466
    UniProt
    Q96KG7
    Pathways
    Regulation of Muscle Cell Differentiation
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