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PSPH Protein (His tag)

Dieses Recombinant PSPH-Protein wird in Escherichia coli (E. coli) produziert.
Produktnummer ABIN7318903

Kurzübersicht für PSPH Protein (His tag) (ABIN7318903)

Target

Alle PSPH Proteine anzeigen
PSPH (Phosphoserine Phosphatase (PSPH))

Protein-Typ

Recombinant

Spezies

  • 8
  • 2
  • 1
  • 1
  • 1
Human

Quelle

  • 4
  • 3
  • 3
  • 2
  • 1
Escherichia coli (E. coli)

Reinheit

> 95 % as determined by reducing SDS-PAGE.
  • Aufreinigungstag / Konjugat

    Dieses PSPH Protein ist gelabelt mit His tag.

    Verwendungszweck

    Recombinant Human PSPH Protein (His Tag)

    Sequenz

    Met 1-Glu225

    Produktmerkmale

    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.

    Endotoxin-Niveau

    < 1.0 EU per μg as determined by the LAL method.
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    Produkt
    Expressionssystem
    Konjugat
    Origin
    Preis ab
    Expressionssystem HEK-293 Cells
    Konjugat His tag
    Origin Human
    Preis ab 12.620,45 €
    Expressionssystem Cell-free protein synthesis (CFPS)
    Konjugat Strep Tag
    Origin Human
    Preis ab 20.480,57 €

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  • Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Frozen, Liquid

    Buffer

    Supplied as a 0.2 μm filtered solution of 50 mM Tris, 250 mM NaCl, 50 mM Imidazole, pH 8.5 .

    Lagerung

    -20 °C

    Informationen zur Lagerung

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

    PSPH (Phosphoserine Phosphatase (PSPH))

    Andere Bezeichnung

    PSPH

    Hintergrund

    Background: 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.

    Synonym: Phosphoserine Phosphatase, PSP, PSPase, L-3-Phosphoserine Phosphatase, O-Phosphoserine Phosphohydrolase, PSPH

    Molekulargewicht

    26.1 kDa

    UniProt

    P78330

    Pathways

    Warburg Effekt
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