| ELK.No | ES16929 |
| Product name | DMP4 rabbit pAb |
| Reactivity | Human; Mouse |
| Applications | WB |
| Other name | |
| Size | 100μL |
| Unit price ($) | 248 |
| Human gene ID | 56975 |
| Human Swiss-Prot | Q8IXL6 |
| Source | Rabbit |
| Isotype | IgG |
| Target | DMP4 |
| Fields | |
| Gene name | FAM20C DMP4 |
| Protein name | DMP4 |
| Human gene link | View Human Gene |
| Human Swiss link | View Human Swiss-Prot |
| Mouse gene ID | 80752 |
| Mouse gene link | View Mouse Gene |
| Mouse Swiss-Prot | Q5MJS3 |
| Mouse Swiss link | View Mouse Swiss-Prot |
| Rat gene ID | |
| Rat gene link | |
| Rat Swiss-Prot | |
| Rat Swiss link | |
| Immunogen | Synthesized peptide derived from human DMP4 AA range: 328-378 |
| Specificity | This antibody detects endogenous levels of DMP4 at Human/Mouse |
| Formulation | Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide. |
| Clonality | Polyclonal |
| Dilution | WB 1:500-2000 |
| Purification | The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen. |
| Concentration | 1 mg/ml |
| Storage stability | -20°C/1 year |
| Molecular Weight (Da) | 64kD |
| Observed band (KD) | |
| Background | This gene encodes a member of the family of secreted protein kinases. The encoded protein binds calcium and phosphorylates proteins involved in bone mineralization. Mutations in this gene are associated with the autosomal recessive disorder Raine syndrome. [provided by RefSeq, Apr 2014], |
| Function | disease:Defects in FAM20C are the cause of Raine syndrome (RNS) [MIM:259775]. RNS is an autosomal recessive osteosclerotic bone dysplasia with neonatal lethal outcome. Clinical features include generalized osteosclerosis, craniofacial dysplasia and microcephaly.,function:Calcium-binding protein which may play a role in dentin mineralization.,similarity:Belongs to the FAM20 family.,tissue specificity:Widely expressed., |
| Subcellular location | Secreted . Golgi apparatus . |
| Expression | Widely expressed. |

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