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MSX1 Protein (Myc-DYKDDDDK Tag)

MSX1 Origin: Human Host: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Catalog No. ABIN2726478
  • Target See all MSX1 Proteins
    MSX1 (Msh Homeobox 1 (MSX1))
    Protein Type
    Recombinant
    Origin
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Human
    Source
    • 12
    • 2
    • 2
    • 1
    HEK-293 Cells
    Purification tag / Conjugate
    This MSX1 protein is labelled with Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Characteristics
    • Recombinant human MSX1 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 MSX1 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
    MSX1 (Msh Homeobox 1 (MSX1))
    Alternative Name
    Msx1 (MSX1 Products)
    Synonyms
    ECTD3 Protein, HOX7 Protein, HYD1 Protein, STHAG1 Protein, AA675338 Protein, AI324650 Protein, Hox-7 Protein, Hox7 Protein, Hox7.1 Protein, msh Protein, CHOX-7 Protein, GHOX-7 Protein, HOX-7 Protein, msh homeobox 1 Protein, MSX1 Protein, Msx1 Protein
    Background
    This gene encodes a member of the muscle segment homeobox gene family. The encoded protein functions as a transcriptional repressor during embryogenesis through interactions with components of the core transcription complex and other homeoproteins. It may also have roles in limb-pattern formation, craniofacial development, particularly odontogenesis, and tumor growth inhibition. Mutations in this gene, which was once known as homeobox 7, have been associated with nonsyndromic cleft lip with or without cleft palate 5, Witkop syndrome, Wolf-Hirschom syndrome, and autosomoal dominant hypodontia.
    Molecular Weight
    31.3 kDa
    NCBI Accession
    NP_002439
    Pathways
    Regulation of Muscle Cell Differentiation, Positive Regulation of Response to DNA Damage Stimulus
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