Species: Hu
Applications: WB, IHC, CyTOF-ready, Flow
Host: Mouse Monoclonal
Species: Hu
Applications: WB, CyTOF-ready, Flow
Host: Goat Polyclonal
Species: Hu, Rt
Applications: WB, ELISA, IHC
Host: Rabbit Polyclonal
Species: Hu
Applications: Binding Activity, Bioactivity
Species: Hu
Applications: PAGE
Species: Hu
Applications: AC
Description
Defects in C1QTNF5 are a cause of late-onset retinal degeneration (LORD). LORD is an autosomal dominant disorder characterized by onset in the fifth to sixth decade with night blindness and punctate yellow-white deposits in the retinal fundus, progressing to severe central and peripheral degeneration, with choroidal neovascularization and chorioretinal atrophy.; Subcellular location: Secreted
Bioinformatics
| Entrez |
Human
Mouse
Rat
|
| Uniprot |
Human
Human
Human
Human
|
| Product By Gene ID |
114902 |
| Alternate Names |
- C1q and tumor necrosis factor related protein 5
- Complement C1q Tumor Necrosis Factor-Related Protein 5 Precursor Variant 3
- CTRP5LORDDKFZp586B0621
- LORD 6
- Myonectin 3
|
Research Areas for C1qTNF5/CTRP5
Find related products by research area and learn more about each of the different research areas below.
Vision
![Immunohistochemistry C1qTNF5/CTRP5 Antibody (332923) [Unconjugated]](http://images.novusbio.com/fullsize2/C1qTNF5_MAB3167_Immunohistochemistry_19941.jpg)
![Intracellular Staining by Flow Cytometry C1qTNF5/CTRP5 Antibody (332923) [Unconjugated]](http://images.novusbio.com/fullsize2/C1qTNF5_MAB3167_Flow_Cytometry_19754.jpg)
![Intracellular Staining by Flow Cytometry C1qTNF5/CTRP5 Antibody [Unconjugated]](http://images.novusbio.com/fullsize2/C1qTNF5_AF3167_Flow_Cytometry_19755.jpg)
![Bioactivity C1qTNF5/CTRP5 [Unconjugated]](http://images.novusbio.com/fullsize2/CTRP5_9510TN_1624.jpg)
