Overview

Description

  • NatureRecombinant
  • SourceWheat germ
  • Amino Acid Sequence
    • AccessionP50221
    • SpeciesHuman
    • SequencePEGSSKARKERTAFTKEQLRELEAEFAHHNYLTRLRRYEIAVNLDLSERQ VKVWFQNRRMKWKRVKGGQPISPNGQDPEDGDSTASPS
    • Molecular weight36 kDa including tags
    • Amino acids165 to 252

Specifications

Our Abpromise guarantee covers the use of ab114872 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

  • Applications

    ELISA

    SDS-PAGE

    Western blot

  • FormLiquid
  • Additional notesProtein concentration is above or equal to 0.05 mg/ml
    Best use within three months from the date of receipt of this protein.
  • Concentration information loading...

Preparation and Storage

  • Stability and Storage

    Shipped on dry ice. Upon delivery aliquot and store at -80ºC. Avoid freeze / thaw cycles.

    pH: 8.00
    Constituents: 0.3% Glutathione, 0.79% Tris HCl

General Info

  • Alternative names
    • Homeobox protein MOX-1
    • MEOX1
    • MEOX1_HUMAN
    • Mesenchyme homeo box 1
    • Mesenchyme homeobox 1
    • MOX 1
    • MOX1
    see all
  • FunctionMesodermal transcription factor that plays a key role in somitogenesis and is specifically required for sclerotome development. Required for maintenance of the sclerotome polarity and formation of the cranio-cervical joints (PubMed:23290072, PubMed:24073994). Binds specifically to the promoter of target genes and regulates their expression. Activates expression of NKX3-2 in the sclerotome. Activates expression of CDKN1A and CDKN2A in endothelial cells, acting as a regulator of vascular cell proliferation. While it activates CDKN1A in a DNA-dependent manner, it activates CDKN2A in a DNA-independent manner. Required for hematopoietic stem cell (HSCs) induction via its role in somitogenesis: specification of HSCs occurs via the deployment of a specific endothelial precursor population, which arises within a sub-compartment of the somite named endotome.
  • Involvement in diseaseKlippel-Feil syndrome 2, autosomal recessive
  • Sequence similaritiesContains 1 homeobox DNA-binding domain.
  • Cellular localizationNucleus. Cytoplasm. Localizes predominantly in the nucleus.
  • Information by UniProt

Recombinant Human MOX1 protein images

  • 12.5% SDS-PAGE showing ab114872 at approximately 35.79kDa.
    Stained with Coomassie Blue.

References for Recombinant Human MOX1 protein (ab114872)

ab114872 has not yet been referenced specifically in any publications.

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Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"