NF2 pSer518 Rabbit Polyclonal Antibody
Other products for "NF2"
Specifications
| Product Data | |
| Applications | IF, WB |
| Recommended Dilution | Western blot: 1/500 - 1/1000. Immunofluorescence: 1/50 - 1/200. |
| Reactivities | Human, Mouse, Rat |
| Host | Rabbit |
| Clonality | Polyclonal |
| Specificity | This antibody detects endogenous levels of p-NF2 protein only when phosphorylated at Ser518. |
| Formulation | Phosphate buffered saline (PBS), pH 7.2. State: Aff - Purified State: Liquid purified Ig fraction Preservative: 0.05% sodium azide |
| Concentration | 1.0 mg/ml |
| Purification | Affinity chromatography (> 95% (by SDS-PAGE) |
| Conjugation | Unconjugated |
| Storage | Store undiluted at 2-8°C for one month or (in aliquots) at -20°C for longer. Avoid repeated freezing and thawing. |
| Stability | Shelf life: one year from despatch. |
| Predicted Protein Size | ~ 70 kDa |
| Gene Name | neurofibromin 2 (merlin) |
| Database Link | |
| Background | Neurofibromatosis type 2 (NF2) is a dominantly inherited disorder characterized by the occurance of bilateral vestibular schwannomas and other central nervous system tumors, including multiple meningiomas. NF2 occurs in about 1 of 40,000 live births. The NF2 gene is highly penetrant; NF2-affected individuals have a 95% chance of developing bilateral vestibular schwannomas. NF2 is distinct from NF1, which is characterized by an incidence of 1 in 4000, maps to chromosome 17 and encodes a protein designated neurofibromin, which is a large protein with a GAP domain. Genetic linkage studies of both sporadic and familial tumors suggest that NF2 is caused by inactivation of a tumor suppressor gene that maps on chromosome 22q12 and encodes a 595 amino acid protein whose function appears to be mediated by interaction with the cytoskeleton. |
| Synonyms | Neurofibromin-2, NF2, SCH, Schwannomin, Schwannomerlin |
| Reference Data | |
| Protein Families | Druggable Genome |
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