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Recombinant Human Protein hairless (HR), Truncated

ACP21123

Number
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High Purity LevelsPrecision and ReliabilityCustomization Options

Specifications


Cat.No ACP21123 Target NameHR
Target SynonymsALUNC; AU; HAIR_HUMAN; Hairless protein; Host range; HR; HSA277165; Protein hairlessFormLyophilized powder
Expression SystemCustom Production. Please inquire and provide the desire expression system.Protein LengthPartial
Purity>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 IDO43593
Background Information
  • Uniprot Id

    O43593

  • Target Species

    Human

  • Target Name

    HR

  • Target Full Name

    Lysine-specific demethylase hairless

  • Target Function

    Histone demethylase that specifically demethylates both mono- and dimethylated 'Lys-9' of histone H3. May act as a transcription regulator controlling hair biology (via targeting of collagens), neural activity, and cell cycle.

  • Target Involvement

    Alopecia universalis congenita (ALUNC); Atrichia with papular lesions (APL); Hypotrichosis 4 (HYPT4)

  • Target Subcellular Location

    Nucleus.

  • Target Tissue Specificity

    Strongest expression of isoforms 1 and 2 is seen in the small intestine, weaker expression in brain and colon, and trace expression is found in liver, pancreas, spleen, thymus, stomach, salivary gland, appendix and trachea. Isoform 1 is always the most ab

  • Target Synonyms

    ALUNC; AU; HAIR_HUMAN; Hairless protein; Host range; HR; HSA277165; Protein hairless

  • Target Background

    This gene encodes a protein that is involved in hair growth. This protein functions as a transcriptional corepressor of multiple nuclear receptors, including thyroid hormone receptor, the retinoic acid receptor-related orphan receptors and the vitamin D receptors, and it interacts with histone deacetylases. The translation of this protein is modulated by a regulatory open reading frame (ORF) that exists upstream of the primary ORF. Mutations in this upstream ORF cause Marie Unna hereditary hypotrichosis (MUHH), an autosomal dominant form of genetic hair loss. Mutations in this gene also cause autosomal recessive congenital alopecia and atrichia with papular lesions, other diseases resulting in hair loss. Two transcript variants encoding different isoforms have been found for this gene.

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