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Human Recombinant Alkaline Phosphatase (from Cells)
Human Recombinant Alkaline Phosphatase (from Cells)
Catalog #: 75789-682
Supplier:  Prosci
CAS Number:  
Human Recombinant Alkaline Phosphatase (from Cells)
Catalog #: 75789-682
Supplier:  Prosci
CAS Number:  
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Specifications

  • Enzyme type:
    Recombinant
  • Source:
    Cells
  • Species:
    Human
  • Size:
    0.05 mg
  • Storage conditions:
    Store at −20 °C, stable for 6 months after receipt. Please minimize freeze−thaw cycles.
  • Endotoxin content:
    <0.1 ng/ug (1 IEU/ug) as determined by LAL test.
  • Enzyme name:
    Alkaline Phosphatase
  • Enzyme synonyms:
    Alkaline Phosphatase, Tissue-Nonspecific Isozyme, AP-TNAP, TNSALP, Alkaline Phosphatase Liver/Bone/Kidney Isozyme, ALPL
  • Purity:
    >95% as determined by reducing SDS-PAGE
  • Molecular weight:
    54.5 kD
  • Sequence:
    Leu18-Ser502
  • Formulation:
    Supplied as a 0.2 µm filtered solution of 20 mM HEPES, 150 mM NaCl, 2 mM MgSO₄, 0.1 mM ZnCl₂, pH 7.5. Always centrifuge tubes before opening. Do not mix by vortex or pipetting. It is not recommended to reconstitute to a concentration less than 100 ug/ml. Dissolve the lyophilized protein in ddH2O. Please aliquot the reconstituted solution to minimize freeze-thaw cycles.
  • Tested applications:
    For Biological Assays
  • Cat. no.:
    75789-682
  • Supplier No.:
    91-503

Specifications

About this item

Alkaline Phosphatase, Tissue-Nonspecific Isozyme (ALPL) is a cell membrane protein which belongs to the alkaline phosphatase family

This recombinant protein can be used for biological assays. For research use only.

Fusion-Tag: C-6 His tag

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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