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Recombinant Human Chromodomain-helicase-DNA-binding protein 2 (CHD2), Truncated

ACP21491

Number
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High Purity LevelsPrecision and ReliabilityCustomization Options

Specifications


Cat.No ACP21491 Target NameCHD2
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 IDO14647
Background Information
  • Uniprot Id

    O14647

  • Target Species

    Human

  • Target Name

    CHD2

  • Target Full Name

    Chromodomain-helicase-DNA-binding protein 2

  • Target Function

    DNA-binding helicase that specifically binds to the promoter of target genes, leading to chromatin remodeling, possibly by promoting deposition of histone H3.3. Involved in myogenesis via interaction with MYOD1: binds to myogenic gene regulatory sequences and mediates incorporation of histone H3.3 prior to the onset of myogenic gene expression, promoting their expression.

  • Target Involvement

    Epileptic encephalopathy, childhood-onset (EEOC)

  • Target Subcellular Location

    Nucleus.

  • Target Protein Families

    SNF2/RAD54 helicase family

  • Target Synonyms

    2810013C04Rik; 2810040A01Rik; 5630401D06Rik; AI851092; ATP dependent helicase CHD2; ATP-dependent helicase CHD2; BC029703; CHD 2; CHD-2; CHD2; CHD2_HUMAN; chromodomain helicase dna binding protein; Chromodomain-helicase-DNA-binding protein 2; DKFZp547I1315; DKFZp686E01200 ; DKFZP781D1727; EC 3.6.1.-; EEOC; FLJ38614

  • Target Background

    The CHD family of proteins is characterized by the presence of chromo (chromatin organization modifier) domains and SNF2-related helicase/ATPase domains. CHD genes alter gene expression possibly by modification of chromatin structure thus altering access of the transcriptional apparatus to its chromosomal DNA template. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene.

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