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Recombinant Human ATP-dependent RNA helicase DDX39A (DDX39A)

ACP21670

Number
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High Purity LevelsPrecision and ReliabilityCustomization Options

Specifications


Cat.No ACP21670 Target NameDDX39A
Target SynonymsDDX39A; DDX39; ATP-dependent RNA helicase DDX39A; EC 3.6.4.13; DEAD box protein 39; Nuclear RNA helicase URH49FormLyophilized powder
Expression SystemCustom Production. Please inquire and provide the desire expression system.Expression Range2-427
Protein LengthFull Length of Mature 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 IDO00148
Background Information
  • Uniprot Id

    O00148

  • Target Species

    Human

  • Target Name

    DDX39A

  • Target Full Name

    ATP-dependent RNA helicase DDX39A

  • Target Function

    Involved in pre-mRNA splicing. Required for the export of mRNA out of the nucleus.

  • Target Subcellular Location

    Nucleus. Cytoplasm. Note=Can translocate to the cytoplasm in the presence of MX1.

  • Target Protein Families

    DEAD box helicase family, DECD subfamily

  • Target Tissue Specificity

    Detected in testis, and at lower levels in brain, kidney, lung, thymus, spleen and salivary gland.

  • Target Synonyms

    DDX39A; DDX39; ATP-dependent RNA helicase DDX39A; EC 3.6.4.13; DEAD box protein 39; Nuclear RNA helicase URH49

  • Target Background

    This gene encodes a member of the DEAD box protein family. These proteins are characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD) and are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure, such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of the DEAD box protein family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. This gene is thought to play a role in the prognosis of patients with gastrointestinal stromal tumors. A pseudogene of this gene is present on chromosome 13. Alternate splicing results in multiple transcript variants. Additional alternatively spliced transcript variants of this gene have been described, but their full-length nature is not known.

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