Telefon:
+49 (0)241 95 163 153
Fax:
+49 (0)241 95 163 155
E-Mail:
orders@antikoerper-online.de

GAMT Protein (His tag)

Dieses Recombinant GAMT-Protein wird in Escherichia coli (E. coli) exprimiert.
Produktnummer ABIN7318555

Kurzübersicht für GAMT Protein (His tag) (ABIN7318555)

Target

Alle GAMT Proteine anzeigen
GAMT (Guanidinoacetate N-Methyltransferase (GAMT))

Protein-Typ

Recombinant

Spezies

  • 6
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Quelle

  • 7
  • 5
  • 2
Escherichia coli (E. coli)

Reinheit

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

    Dieses GAMT Protein ist gelabelt mit His tag.

    Verwendungszweck

    Recombinant Human GAMT Protein (His Tag)

    Sequenz

    Met 1-Gly236

    Produktmerkmale

    Recombinant Human Guanidinoacetate N-methyltransferase is produced by our E.coli expression system and the target gene encoding Met1-Gly236 is expressed with a 6His tag at the N-terminus, 6His tag at the C-terminus.

    Endotoxin-Niveau

    < 1.0 EU per μg as determined by the LAL method.
  • Möchten Sie weitere Optionen für dieses Protein ?

    !
    Entdecken Sie unsere vordefinierten maßgeschneiderten Proteine und Proteinservices!

    Ihr Projekt erfordert weitere Anpassungen? Kontaktieren Sie uns und entdecken Sie unsere maßgeschneiderten Proteinlösungen

  • Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Frozen, Liquid

    Buffer

    Supplied as a 0.2 μm filtered solution of 20 mM TrisHCl,1 mMDTT, pH 8.0 .

    Lagerung

    -20 °C

    Informationen zur Lagerung

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

    GAMT (Guanidinoacetate N-Methyltransferase (GAMT))

    Andere Bezeichnung

    GAMT

    Hintergrund

    Background: GAMT is a methyltransferase which belongs to the class I-like SAM-binding methyltransferase superfamily. It contains one RMT2 (arginine N-methyltransferase 2-like) domain and is expressed in liver. GAMT converts guanidoacetate to creatine, using S-adenosylmethionine as the methyl donor. Defects in GAMT are the cause of guanidinoacetate methyltransferase deficiency, which is an autosomal recessive disorder characterized by developmental delay/regression, mental retardation, severe disturbance of expressive and cognitive speech, intractable seizures and movement disturbances, severe depletion of creatine/phosphocreatine in the brain, and accumulation of guanidinoacetic acid in brain and body fluids.

    Synonym: Guanidinoacetate N-methyltransferase, GAMT, PIG2,TP53I2

    Molekulargewicht

    29.5 kDa

    UniProt

    Q14353
Sie sind hier:
Chat with us!