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| Cat.No | ACP21670 | Target Name | DDX39A |
|---|---|---|---|
| Target Synonyms | DDX39A; DDX39; ATP-dependent RNA helicase DDX39A; EC 3.6.4.13; DEAD box protein 39; Nuclear RNA helicase URH49 | Form | Lyophilized powder |
| Expression System | Custom Production. Please inquire and provide the desire expression system. | Expression Range | 2-427 |
| Protein Length | Full Length of Mature Protein | Purity | >85% (SDS-PAGE) |
| Storage Buffer | 5%-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. |
| Target Species | Human | Uniprot ID | O00148 |
|---|
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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