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DHX16 (NM_003587) Human Tagged ORF Clone Lentiviral Particle
CAT＃: RC202912L4V
- LentiORF®
-
Lenti ORF particles, DHX16 (mGFP-tagged) - Human DEAH (Asp-Glu-Ala-His) box polypeptide 16 (DHX16), transcript variant 1, 200ul, >10^7 TU/mL
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CNY 12,540.00
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规格
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Specifications
| Product Data | |
| Product Name | DHX16 (NM_003587) Human Tagged ORF Clone Lentiviral Particle |
| Synonyms | DBP2; DDX16; NMOAS; PRO2014; Prp2; PRP8; PRPF2 |
| Vector | pLenti-C-mGFP-P2A-Puro |
| ACCN | NM_003587 |
| ORF Size | 3126 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(RC202912).
|
| 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_003587.3 |
| RefSeq Size | 3477 bp |
| RefSeq ORF | 3126 bp |
| Locus ID | 8449 |
| Domains | DEAD, helicase_C, HA2 |
| Protein Pathways | Spliceosome |
| MW | 119.4 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 a functional homolog of fission yeast Prp8 protein involved in cell cycle progression. This gene is mapped to the MHC region on chromosome 6p21.3, a region where many malignant, genetic and autoimmune disease genes are linked. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2018] |
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