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DYRK1A (NM_001396) Human Tagged ORF Clone Lentiviral Particle
CAT＃: RC212584L3V
- LentiORF®
-
Lenti ORF particles, DYRK1A (Myc-DDK-tagged)-Human dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1A (DYRK1A), transcript variant 1, 200ul, >10^7 TU/mL
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CNY 14,250.00
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规格
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Specifications
| Product Data | |
| Product Name | DYRK1A (NM_001396) Human Tagged ORF Clone Lentiviral Particle |
| Synonyms | DYRK; DYRK1; HP86; MNB; MNBH; MRD7 |
| Vector | pLenti-C-Myc-DDK-P2A-Puro |
| ACCN | NM_001396 |
| ORF Size | 2289 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(RC212584).
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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_001396.2 |
| RefSeq Size | 5010 bp |
| RefSeq ORF | 2292 bp |
| Locus ID | 1859 |
| Domains | pkinase, TyrKc, S_TKc |
| Protein Families | Druggable Genome, Protein Kinase |
| MW | 85.4 kDa |
| Gene Summary | This gene encodes a member of the Dual-specificity tyrosine phosphorylation-regulated kinase (DYRK) family. This member contains a nuclear targeting signal sequence, a protein kinase domain, a leucine zipper motif, and a highly conservative 13-consecutive-histidine repeat. It catalyzes its autophosphorylation on serine/threonine and tyrosine residues. It may play a significant role in a signaling pathway regulating cell proliferation and may be involved in brain development. This gene is a homolog of Drosophila mnb (minibrain) gene and rat Dyrk gene. It is localized in the Down syndrome critical region of chromosome 21, and is considered to be a strong candidate gene for learning defects associated with Down syndrome. Alternative splicing of this gene generates several transcript variants differing from each other either in the 5' UTR or in the 3' coding region. These variants encode at least five different isoforms. [provided by RefSeq, Jul 2008] |
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