Species: Hu
Applications: WB, Simple Western
Host: Goat Polyclonal
Species: Hu
Applications: ICC/IF, IHC
Host: Mouse Monoclonal
Species: Hu
Applications: WB
Host: Mouse Monoclonal
Species: Mu
Applications: Bioactivity
Species: Hu
Applications: Bioactivity
Description
ROR2 is encoded by this gene is a receptor protein tyrosine kinase and type I transmembrane protein that belongs to the ROR subfamily of cell surface receptors. The protein may be involved in the early formation of the chondrocytes and may be required for cartilage and growth plate development. Mutations in this gene can cause brachydactyly type B, a skeletal disorder characterized by hypoplasia/aplasia of distal phalanges and nails. In addition, mutations in this gene can cause the autosomal recessive form of Robinow syndrome, which is characterized by skeletal dysplasia with generalized limb bone shortening, segmental defects of the spine, brachydactyly, and a dysmorphic facial appearance.
Bioinformatics
| Entrez |
Human
|
| Uniprot |
Human
Human
Human
|
| Product By Gene ID |
4920 |
| Alternate Names |
- BDB
- BDB1
- EC 2.7.10.1
- MGC163394
- neurotrophic tyrosine kinase receptor-related 2
- Neurotrophic tyrosine kinase, receptor-related 2
- NTRKR2tyrosine-protein kinase transmembrane receptor ROR2
- receptor tyrosine kinase-like orphan receptor 2
|
![Western Blot ROR2 Antibody [Unconjugated]](http://images.novusbio.com/fullsize2/ROR2_AF2064_Western_Blot_11177.jpg)
![Simple Western ROR2 Antibody [Unconjugated]](http://images.novusbio.com/fullsize2/ROR2_AF2064_Simple_Western_16763.jpg)
![Binding Activity ROR2 [Unconjugated]](http://images.novusbio.com/fullsize/11425-ro_recombinant-mouse-ror2-mfc-chimera-protein-cf-binding-activity-2292023122515.jpg)
![SDS-PAGE ROR2 [Unconjugated]](http://images.novusbio.com/fullsize/11425-ro_recombinant-mouse-ror2-mfc-chimera-protein-cf-sds-page-2292023125436..jpg)