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Recombinant Human Bromodomain and WD repeat-containing protein 1 (BRWD1), Truncated

ACP11737

Number
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High Purity LevelsPrecision and ReliabilityCustomization Options

Specifications


Cat.No ACP11737 Target NameBRWD1
FormLyophilized powderExpression SystemCustom Production. Please inquire and provide the desire expression system.
Protein LengthPartialPurity>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 IDQ9NSI6
Background Information
  • Uniprot Id

    Q9NSI6

  • Target Species

    Human

  • Target Name

    BRWD1

  • Target Full Name

    Bromodomain and WD repeat-containing protein 1

  • Target Function

    May be a transcriptional activator. May be involved in chromatin remodeling. Plays a role in the regulation of cell morphology and cytoskeletal organization. Required in the control of cell shape.

  • Target Subcellular Location

    Cytoplasm. Nucleus.

  • Target Tissue Specificity

    Ubiquitously expressed.

  • Target Synonyms

    Bromodomain and WD repeat domain containing protein 1; Bromodomain and WD repeat-containing protein 1; Brwd1; BRWD1_HUMAN; C21orf107; cAMP response element binding and beta tranducin family; FLJ11315; N143; Transcriptional unit N143; WD repeat protein; WD repeat-containing protein 9; WDR9

  • Target Background

    This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD) residues which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes including cell cycle progression, signal transduction, apoptosis, and gene regulation. This protein contains 2 bromodomains and multiple WD repeats. This gene is located within the Down syndrome region-2 on chromosome 21. Alternative splicing of this gene generates multiple transcript variants encoding distinct isoforms. In mouse, this gene encodes a nuclear protein that has a polyglutamine-containing region that functions as a transcriptional activation domain which may regulate chromatin remodelling and associates with a component of the SWI/SNF chromatin remodelling complex.

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