Name: Human Alkaline Phosphatase/ALPL Recombinant Protein (His Tag)

Synonyms: Alkaline Phosphatase;Tissue-Nonspecific Isozyme;AP-TNAP;TNSALP;Alkaline Phosphatase Liver/Bone/Kidney Isozyme;ALPL;HOPS;TNAP

Expression host: HEK293 Cells

Sequence: Leu18-Ser502

Accesstion: P05186

Species: Human

Mol_Mass: 54.5 kDa

AP_Mol_Mass: 65-90 kDa

Tag: C-His

Purity: > 95 % as determined by reducing SDS-PAGE.


Storage: Store at

Shipping: This product is provided as liquid. It is shipped at frozen temperature with blue ice/gel packs. Upon receipt, store it immediately at

Formulation: Supplied as a 0.2 μm filtered solution of 20mM Tris-HCl,1mM DTT,1mM EDTA,500mM NaCl,0.1%Trition X-100,pH 8.0.

Reconstitution: Not Applicable

Background: Alkaline Phosphatase, Tissue-Nonspecific Isozyme (ALPL) is a cell membrane protein which belongs to the Alkaline Phosphatase family. There are at least four distinct but related Alkaline Phosphatases in humans: intestinal AP (IAP), placental AP(PLAP), germ cell AP (GCAP) and their genes are clustered on chromosome 2, tissue-nonspecific isozyme (TNAP) which gene is located on chromosome 1. Alkaline Phosphatases (APs) are dimeric enzymes, it catalyze the hydrolysis of phosphomonoesters with release of inorganic phosphate. The native ALPL is a glycosylated homodimer attached to the membrane through a GPI-anchor. This isozyme may play a role in skeletal mineralization. Mutations in ALPL gene have been linked directly to different forms of hypophosphatasia,characterized by poorly mineralized cartilage and bones, and this disorder can vary depending on the specific mutation since this determines age of onset and severity of symptoms.

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