Prion protein PrP (PRNP) Mouse Monoclonal Antibody [Clone ID: EM-20]
CAT#: AM26026PU-N
Prion protein PrP (PRNP) mouse monoclonal antibody, clone EM-20, Aff - Purified
Other products for "PRNP"
Specifications
| Product Data | |
| Clone Name | EM-20 |
| Applications | IHC, WB |
| Recommended Dilution | Western blot: 0.5 μg/ml (Non-reducing conditions are essential). This clone has been described to work in Immunohistochemistry on Paraffin Sections (10 µg/ml). |
| Reactivities | Human |
| Host | Mouse |
| Isotype | IgG2a |
| Clonality | Monoclonal |
| Immunogen | Recombinant human prion protein |
| Specificity | The Mouse monoclonal antibody EM-20 recognizes Human prion protein (PrP). Diglycosylated form of PrP has ~40 kDa, monoglycosylated form ~30 kDa, and nonglycosylated form ~19-21 kDa. This antibody is suitable for discrimination between normal cellular prion protein (PrPc) and its conformationally changed form (PrPSc) prion protein. |
| Formulation | PBS, pH~7.4 State: Aff - Purified State: Liquid purified Ig fraction (> 95% pure by SDS-PAGE) Preservative: 15mM Sodium Azide |
| Concentration | lot specific |
| Purification | Affinity Chromatography on Protein A |
| 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. |
| Gene Name | Homo sapiens prion protein (PRNP), transcript variant 1 |
| Database Link | |
| Background | The mouse monoclonal antibody EM-20 recognizes human prion protein (PrP). Diglycosylated form of PrP has ~ 40 kDa, monoglycosylated form ~ 30 kDa, and nonglycosylated form ~ 19-21 kDa. This antibody is suitable for discrimination between normal cellular prion protein (PrPc) and its conformationally changed form (PrPSc) prion protein. |
| Synonyms | Major prion protein, PrP27-30, PrP33-35C, ASCR, PRNP, PRIP |
| Reference Data | |
| Protein Families | ES Cell Differentiation/IPS, Stem cell - Pluripotency, Transmembrane |
| Protein Pathways | Prion diseases |
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