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Mesp2 antibody (AA 37-94)

Mesp2 Reactivity: Human ELISA, WB Host: Mouse Monoclonal unconjugated
Catalog No. ABIN1845976
  • Target See all Mesp2 Antibodies
    Mesp2 (Mesoderm Posterior 2 Homolog (Mesp2))
    Binding Specificity
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 37-94
    Reactivity
    • 5
    • 4
    • 2
    Human
    Host
    • 6
    • 2
    Mouse
    Clonality
    • 6
    • 2
    Monoclonal
    Conjugate
    • 8
    This Mesp2 antibody is un-conjugated
    Application
    • 6
    • 5
    • 1
    ELISA, Western Blotting (WB)
    Purification
    Purified antibody
    Immunogen
    Purified recombinant fragment of human MESP2 (AA: 37-94) expressed in E. Coli.
    Isotype
    IgG1
    Top Product
    Discover our top product Mesp2 Primary Antibody
  • Application Notes
    Optimal working dilution should be determined by the investigator.
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1.0 mg/mL
    Buffer
    PBS with 0.05 % sodium azide and 0.5 % protein stabilizer.
    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
    Aliquot and store at -20 °C. Avoid repeated freeze/thaw cycles.
  • Target
    Mesp2 (Mesoderm Posterior 2 Homolog (Mesp2))
    Alternative Name
    MESP2 (Mesp2 Products)
    Synonyms
    bHLHc6 antibody, SCDO2 antibody, mesoderm posterior 2 antibody, mesoderm posterior bHLH transcription factor 2 antibody, Mesp2 antibody, MESP2 antibody
    Background
    This gene encodes a member of the bHLH family of transcription factors and plays a key role in defining the rostrocaudal patterning of somites via interactions with multiple Notch signaling pathways. This gene is expressed in the anterior presomitic mesoderm and is downregulated immediately after the formation of segmented somites. This gene also plays a role in the formation of epithelial somitic mesoderm and cardiac mesoderm. Mutations in the MESP2 gene cause autosomal recessive spondylocostal dystosis 2 (SCD02).
    Molecular Weight
    41.8 kDa
    Gene ID
    145873
    UniProt
    Q0VG99
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