ALPP (clone 3E5), anti-human
€394.00
In stock
SKU
253021
Catalog Nr.: 253021
Size: 0.1 ml
Isotype: Mouse IgG2b
Applications: WB
Size: 0.1 ml
Isotype: Mouse IgG2b
Applications: WB
Protein Family: Enzymes
Pathway and Disease: Cofactor and Vitamin Metabolism;
Description:
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.
Alternate Names: AP, IAP, ALPI, Intestinal alkaline phosphatase
Application Notes: WB: 1:200-1:1000
Accession No.: P19111
Antigen: Purified recombinant fragment of human ALPP expressed in E. coli.
Format: Each vial contains 0.1 ml ascitic fluid with 0.03% sodium azide.
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.
Pathway and Disease: Cofactor and Vitamin Metabolism;
Description:
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.
Alternate Names: AP, IAP, ALPI, Intestinal alkaline phosphatase
Application Notes: WB: 1:200-1:1000
Accession No.: P19111
Antigen: Purified recombinant fragment of human ALPP expressed in E. coli.
Format: Each vial contains 0.1 ml ascitic fluid with 0.03% sodium azide.
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.
| Is Featured? | No |
|---|
Write Your Own Review