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DDX11 (NM_004399) Human Tagged ORF Clone Lentiviral Particle
CAT＃: RC219362L4V
- LentiORF®
-
Lenti ORF particles, DDX11 (mGFP-tagged)-Human DEAD/H (Asp-Glu-Ala-Asp/His) box polypeptide 11 (DDX11), transcript variant 2, 200ul, >10^7 TU/mL
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CNY 17,195.00
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Specifications
| Product Data | |
| Product Name | DDX11 (NM_004399) Human Tagged ORF Clone Lentiviral Particle |
| Synonyms | CHL1; CHLR1; KRG2; WABS |
| Vector | pLenti-C-mGFP-P2A-Puro |
| ACCN | NM_004399 |
| ORF Size | 2568 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(RC219362).
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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_004399.2 |
| RefSeq Size | 3755 bp |
| RefSeq ORF | 2571 bp |
| Locus ID | 1663 |
| Domains | DEXDc2, HELICc2 |
| Protein Families | Stem cell - Pluripotency |
| MW | 95.9 kDa |
| Gene Summary | DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), 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 this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. This gene encodes a DEAD box protein, which is an enzyme that possesses both ATPase and DNA helicase activities. This gene is a homolog of the yeast CHL1 gene, and may function to maintain chromosome transmission fidelity and genome stability. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2008] |
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