UAP56 (DDX39B) (NM_004640) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC201248L3V
- LentiORF®
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Lenti ORF particles, DDX39B (Myc-DDK tagged) - Human DEAD (Asp-Glu-Ala-Asp) box polypeptide 39B (DDX39B), transcript variant 1, 200ul, >10^7 TU/mL
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CNY 8,930.00
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CNY 2,700.00
Specifications
Product Data | |
Product Name | UAP56 (DDX39B) (NM_004640) Human Tagged ORF Clone Lentiviral Particle |
Synonyms | BAT1; D6S81E; UAP56 |
Vector | pLenti-C-Myc-DDK-P2A-Puro |
ACCN | NM_004640 |
ORF Size | 1284 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC201248).
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OTI Disclaimer | The molecular sequence of this clone aligns with the gene accession number as a point of reference only. However, individual transcript sequences of the same gene can differ through naturally occurring variations (e.g. polymorphisms), each with its own valid existence. This clone is substantially in agreement with the reference, but a complete review of all prevailing variants is recommended prior to use. More info |
OTI Annotation | This clone was engineered to express the complete ORF with an expression tag. Expression varies depending on the nature of the gene. |
Reference Data | |
RefSeq | NM_004640.5, NP_004631.1 |
RefSeq Size | 2174 bp |
RefSeq ORF | 1287 bp |
Locus ID | 7919 |
Domains | DEAD, helicase_C |
Protein Pathways | Spliceosome |
MW | 49 kDa |
Gene Summary | This gene encodes a member of the DEAD box family of RNA-dependent ATPases that mediate ATP hydrolysis during pre-mRNA splicing. The encoded protein is an essential splicing factor required for association of U2 small nuclear ribonucleoprotein with pre-mRNA, and it also plays an important role in mRNA export from the nucleus to the cytoplasm. This gene belongs to a cluster of genes localized in the vicinity of the genes encoding tumor necrosis factor alpha and tumor necrosis factor beta. These genes are all within the human major histocompatibility complex class III region. Mutations in this gene may be associated with rheumatoid arthritis. Alternative splicing results in multiple transcript variants. Related pseudogenes have been identified on both chromosomes 6 and 11. Read-through transcription also occurs between this gene and the upstream ATP6V1G2 (ATPase, H+ transporting, lysosomal 13kDa, V1 subunit G2) gene. [provided by RefSeq, Feb 2011] |
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FAQs |
SDS |