DDR2 (NM_001014796) Human Tagged ORF Clone Lentiviral Particle
- LentiORF®
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Specifications
| Product Data | |
| Type | Human Tagged ORF Clone Lentiviral Particle |
|---|---|
| Tag | Myc-DDK |
| Target Symbol | DDR2 |
| Synonyms | MIG20a; NTRKR3; TKT; TYRO10; WRCN |
| Vector | pLenti-C-Myc-DDK-P2A-Puro |
| Mammalian Cell Selection | Puromycin |
| Sequence Data | |
| ACCN | NM_001014796 |
| ORF Size | 2565 bp |
| 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. |
| Shipping | Dry Ice |
| Reference Data | |
| RefSeq | NM_001014796.1 |
| RefSeq Size | 3252 bp |
| RefSeq ORF | 2568 bp |
| Locus ID | 4921 |
| UniProt ID | Q16832 |
| Cytogenetics | 1q23.3 |
| Protein Families | Druggable Genome, Protein Kinase, Transmembrane |
| MW | 96.7 kDa |
| Summary | This gene encodes a member of the discoidin domain receptor subclass of the receptor tyrosine kinase (RTKs) protein family. RTKs play a key role in the communication of cells with their microenvironment. The encoded protein is a collagen-induced receptor that activates signal transduction pathways involved in cell adhesion, proliferation, and extracellular matrix remodeling. This protein is expressed in numerous cell types and may alos be involved in wound repair and regulate tumor growth and invasiveness. Mutations in this gene are the cause of short limb-hand type spondylometaepiphyseal dysplasia. provided by RefSeq, Aug 2017 |
Reviews
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Resources
Citations
Yeung, Shanker, Sohail et al
J. Mol. Biol. (2018) 431 (2), 368-390 DOI: 10.1016/j.jmb.2018.11.015
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