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ALPL Protein (His tag)

This Recombinant ALPL protein is produced in Human Cells.
Catalog No. ABIN7318146

Quick Overview for ALPL Protein (His tag) (ABIN7318146)

Target

See all ALPL Proteins
ALPL (Alkaline Phosphatase, Liver/bone/kidney (ALPL))

Protein Type

Recombinant

Origin

  • 13
  • 5
  • 3
  • 2
  • 1
  • 1
Human

Source

  • 10
  • 6
  • 4
  • 2
  • 1
  • 1
  • 1
Human Cells

Purity

> 95 % as determined by reducing SDS-PAGE.
  • Purification tag / Conjugate

    This ALPL protein is labelled with His tag.

    Purpose

    Recombinant Human Alkaline Phosphatase/ALPL Protein (His Tag)

    Sequence

    Leu18-Ser502

    Characteristics

    Recombinant Human Alkaline Phosphatase, Tissue-Nonspecific Isozyme is produced by our Mammalian expression system and the target gene encoding Leu18-Ser502 is expressed with a 6His tag at the C-terminus.

    Endotoxin Level

    < 1.0 EU per μg as determined by the LAL method.
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  • Restrictions

    For Research Use only
  • Format

    Frozen, Liquid

    Buffer

    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.

    Storage

    -20 °C

    Storage Comment

    Store at < -20°C, stable for 6 months. Please minimize freeze-thaw cycles.
  • Target

    ALPL (Alkaline Phosphatase, Liver/bone/kidney (ALPL))

    Alternative Name

    Alkaline Phosphatase/ALPL

    Background

    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.

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

    Molecular Weight

    54.5 kDa

    UniProt

    P05186
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