AP (Alkaline phosphatase) is a tissue-nonspecific isozyme that plays a role in skeletal mineralization. Defects in AP are a cause of hypophosphatasia (HOPS). HOPS is an inherited metabolic bone disease characterized by defective skeletal mineralization.
- Clonality: Monoclonal
- Host: Mouse
- Reactivity: Human
- Antigen: "Purified recombinant fragment of human ALPP expressed in E. coli.
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- Clone: 3E5
- Isotype: Mouse IgG2b
- Gene: P19111
- Quantity: 0.1 ml
- Storage: Store at 4°C for short term use only. Store at -20°C for storage over 1 month. Product is guaranteed 6 months from the date of shipment.
