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Recombinant Human POU domain, class 4, transcription factor 3 (POU4F3)

ACP18026

Number
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High Purity LevelsPrecision and ReliabilityCustomization Options

Specifications


Cat.No ACP18026 Target NamePOU4F3
FormLyophilized powderExpression SystemCustom Production. Please inquire and provide the desire expression system.
Expression Range1-338Protein LengthFull length protein
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 IDQ15319
Background Information
  • Uniprot Id

    Q15319

  • Target Species

    Human

  • Target Name

    POU4F3

  • Target Full Name

    POU domain, class 4, transcription factor 3

  • Target Function

    Acts as a transcriptional activator. Acts by binding to sequences related to the consensus octamer motif 5'-ATGCAAAT-3' in the regulatory regions of its target genes. Involved in the auditory system development, required for terminal differentiation of hair cells in the inner ear.

  • Target Involvement

    Deafness, autosomal dominant, 15 (DFNA15)

  • Target Subcellular Location

    Nucleus. Cytoplasm.

  • Target Protein Families

    POU transcription factor family, Class-4 subfamily

  • Target Tissue Specificity

    Brain. Seems to be specific to the retina.

  • Target Synonyms

    Brain specific homeobox/POU domain protein 3C; Brain-3C; Brain-specific homeobox/POU domain protein 3C; BRN 3C; Brn-3C; BRN3C; class 4; DFNA 15; DFNA15; MGC138412; PO4F3_HUMAN; POU class 4 homeobox 3; POU domain; POU domain class 4 transcription factor 3; POU4F3; transcription factor 3

  • Target Background

    This gene encodes a member of the POU-domain family of transcription factors. POU-domain proteins have been observed to play important roles in control of cell identity in several systems. This protein is found in the retina and may play a role in determining or maintaining the identities of a small subset of visual system neurons. Defects in this gene are the cause of non-syndromic sensorineural deafness autosomal dominant type 15.

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