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PSPH Protein (His tag)

This Recombinant PSPH protein is produced in Escherichia coli (E. coli).
Catalog No. ABIN7318903
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$246.18
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Quick Overview for PSPH Protein (His tag) (ABIN7318903)

Target

See all PSPH Proteins
PSPH (Phosphoserine Phosphatase (PSPH))

Protein Type

Recombinant

Origin

  • 12
  • 2
  • 1
  • 1
  • 1
Human

Source

  • 7
  • 3
  • 3
  • 2
  • 1
  • 1
Escherichia coli (E. coli)

Purity

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

    This PSPH protein is labelled with His tag.

    Purpose

    Recombinant Human PSPH Protein (His Tag)

    Sequence

    Met 1-Glu225

    Characteristics

    Recombinant Human Phosphoserine Phosphatase is produced by our E.coli expression system and the target gene encoding Met1-Glu225 is expressed with a 6His tag at the C-terminus.

    Sterility

    0.2 μm filtered

    Endotoxin Level

    < 1.0 EU per μg of the protein as determined by the LAL method.

    Biological Activity Comment

    Not validated for activity
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  • Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Supplied as a 0.2 μm filtered solution of 20 mM Tris-HCl, 4M Urea, 5 mM EDTA, pH 8.0.

    Storage

    -20 °C

    Storage Comment

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

    Expiry Date

    6 months
  • Target

    PSPH (Phosphoserine Phosphatase (PSPH))

    Alternative Name

    PSPH

    Background

    L-3-Phosphoserine Phosphatase,O-Phosphoserine Phosphohydrolase,PSP,PSPH,PSPase,Phosphoserine Phosphatase,Phosphoserine phosphatase (PSP) is an enzyme that belongs to the serB family. PSPH catalyzes magnesium-dependent hydrolysis of L-phosphoserine and is also involved in an exchange reaction between L-serine and L-phosphoserine. The reaction mechanism proceeds via the formation of a phosphoryl-enzyme intermediates. Deficiency of this protein is thought to be linked to Williams syndrome. A disorder that results in pre- and postnatal growth retardation, moderate psychomotor retardation and facial features suggestive of Williams syndrome.

    Molecular Weight

    Calculated MW: 26.1 kDa

    Observed MW: 25-30 kDa

    Gene ID

    5723

    UniProt

    P78330

    Pathways

    Warburg Effect
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