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MESDC2 antibody

MESDC2 Reactivity: Human, Mouse WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7257489
  • Target See all MESDC2 Antibodies
    MESDC2 (Mesoderm Development Candidate 2 (MESDC2))
    Reactivity
    • 28
    • 4
    • 2
    • 1
    Human, Mouse
    Host
    • 26
    • 3
    • 1
    Rabbit
    Clonality
    • 29
    • 1
    Polyclonal
    Conjugate
    • 13
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This MESDC2 antibody is un-conjugated
    Application
    • 23
    • 15
    • 15
    • 13
    • 5
    • 1
    • 1
    • 1
    Western Blotting (WB)
    Characteristics
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogen
    Recombinant fusion protein of human MESDC2 (NP_055969.1).
    Isotype
    IgG
    Top Product
    Discover our top product MESDC2 Primary Antibody
  • Application Notes
    WB 1:500-1:2000
    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
    MESDC2 (Mesoderm Development Candidate 2 (MESDC2))
    Alternative Name
    MESDC2 (MESDC2 Products)
    Synonyms
    MGC115616 antibody, MESDC2 antibody, BOCA antibody, MESD antibody, 2210015O11Rik antibody, AW537813 antibody, mKIAA0081 antibody, mesd antibody, msd antibody, zgc:158636 antibody, mesoderm development LRP chaperone antibody, mesoderm development LRP chaperone L homeolog antibody, mesoderm development candidate 2 antibody, MESD antibody, mesd.L antibody, CpipJ_CPIJ010816 antibody, Tsp_04045 antibody, mesd antibody, Mesd antibody, MESDC2 antibody
    Background
    MESD (Mesoderm Development LRP Chaperone) is a Protein Coding gene. Diseases associated with MESD include Osteogenesis Imperfecta, Type Xx and Epilepsy, Nocturnal Frontal Lobe, 2. Among its related pathways are Wnt / Hedgehog / Notch.
    Molecular Weight

    Observed_MW: 26 kDa

    Calculated_MW: 26 kDa

    Gene ID
    23184
    UniProt
    Q14696
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