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Recombinant Human Homeobox protein DLX-5 (DLX5)

ACP22776

Number
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High Purity LevelsPrecision and ReliabilityCustomization Options

Specifications


Cat.No ACP22776 Target NameDLX5
Target SynonymsDLX5Homeobox protein DLX-5FormLyophilized powder
Expression SystemCustom Production. Please inquire and provide the desire expression system.Expression Range1-289
Protein LengthFull length proteinPurity>85% (SDS-PAGE)
Storage Buffer5%-50% glycerol. Lyophilized powder form: the buffer before lyophilization is Tris/PBS-based buffer, 6% Trehalose, Liquid form: default storage buffer is Tris/PBS-based buffer, pH 8.0.

Immunogen Information


Target SpeciesHumanUniprot IDP56178
Background Information
  • Uniprot Id

    P56178

  • Target Species

    Human

  • Target Name

    DLX5

  • Target Full Name

    Homeobox protein DLX-5

  • Target Function

    Transcriptional factor involved in bone development. Acts as an immediate early BMP-responsive transcriptional activator essential for osteoblast differentiation. Stimulates ALPL promoter activity in a RUNX2-independent manner during osteoblast differentiation. Stimulates SP7 promoter activity during osteoblast differentiation. Promotes cell proliferation by up-regulating MYC promoter activity. Involved as a positive regulator of both chondrogenesis and chondrocyte hypertrophy in the endochondral skeleton. Binds to the homeodomain-response element of the ALPL and SP7 promoter. Binds to the MYC promoter. Requires the 5'-TAATTA-3' consensus sequence for DNA-binding.

  • Target Involvement

    Split-hand/foot malformation 1 with sensorineural hearing loss, autosomal recessive (SHFM1D)

  • Target Subcellular Location

    Nucleus.

  • Target Protein Families

    Distal-less homeobox family

  • Target Synonyms

    DLX5Homeobox protein DLX-5

  • Target Background

    This gene encodes a member of a homeobox transcription factor gene family similiar to the Drosophila distal-less gene. The encoded protein may play a role in bone development and fracture healing. Mutation in this gene, which is located in a tail-to-tail configuration with another member of the family on the long arm of chromosome 7, may be associated with split-hand/split-foot malformation.

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