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DCAMKL2 (DCLK2) (NM_001040261) Human Tagged ORF Clone Lentiviral Particle
CAT＃: RC219994L3V
- LentiORF®
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Lenti ORF particles, DCLK2 (Myc-DDK-tagged)-Human doublecortin-like kinase 2 (DCLK2), transcript variant 2, 200ul, >10^7 TU/mL
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CNY 14,250.00
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Specifications
| Product Data | |
| Product Name | DCAMKL2 (DCLK2) (NM_001040261) Human Tagged ORF Clone Lentiviral Particle |
| Synonyms | CL2; CLICK-II; CLICK2; CLIK2; DCAMKL2; DCDC3; DCDC3B; DCK2 |
| Vector | pLenti-C-Myc-DDK-P2A-Puro |
| ACCN | NM_001040261 |
| ORF Size | 2349 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(RC219994).
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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_001040261.4 |
| RefSeq Size | 4316 bp |
| RefSeq ORF | 2352 bp |
| Locus ID | 166614 |
| Protein Families | Druggable Genome, Protein Kinase |
| MW | 85.4 kDa |
| Gene Summary | This gene encodes a member of the protein kinase superfamily and the doublecortin family. The protein encoded by this gene contains two N-terminal doublecortin domains, which bind microtubules and regulate microtubule polymerization, a C-terminal serine/threonine protein kinase domain, which shows substantial homology to Ca2+/calmodulin-dependent protein kinase, and a serine/proline-rich domain in between the doublecortin and the protein kinase domains, which mediates multiple protein-protein interactions. The microtubule-polymerizing activity of the encoded protein is independent of its protein kinase activity. Mouse studies show that the DCX gene, another family member, and this gene share function in the establishment of hippocampal organization and that their absence results in a severe epileptic phenotype and lethality, as described in human patients with lissencephaly. Multiple alternatively spliced transcript variants have been identified. [provided by RefSeq, Sep 2010] |
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