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MSX1 Protein (Myc-DYKDDDDK Tag)

This Recombinant MSX1 protein is produced in HEK-293 Cells.
Catalog No. ABIN2726478
$1,112.40
Plus shipping costs $50.00, if applicable $20.00 dry ice
20 μg
Shipping to: United States
Delivery in 16 to 17 Business Days

Quick Overview for MSX1 Protein (Myc-DYKDDDDK Tag) (ABIN2726478)

Target

See all MSX1 Proteins
MSX1 (Msh Homeobox 1 (MSX1))

Protein Type

Recombinant

Origin

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Human

Source

  • 12
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HEK-293 Cells

Application

Antibody Production (AbP), Standard (STD)

Purity

> 80 % as determined by SDS-PAGE and Coomassie blue staining
  • Purification tag / Conjugate

    This MSX1 protein is labelled with Myc-DYKDDDDK Tag.

    Characteristics

    • Recombinant human MSX1 protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
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    Origin Human
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  • 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

    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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