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GAMT Protein (His tag)

This Recombinant GAMT protein is expressed in Escherichia coli (E. coli).
Catalog No. ABIN7318555
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Quick Overview for GAMT Protein (His tag) (ABIN7318555)

Target

See all GAMT Proteins
GAMT (Guanidinoacetate N-Methyltransferase (GAMT))

Protein Type

Recombinant

Origin

  • 10
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Source

  • 11
  • 5
  • 1
  • 1
Escherichia coli (E. coli)

Purity

> 90 % as determined by reducing SDS-PAGE.
  • Purification tag / Conjugate

    This GAMT protein is labelled with His tag.

    Purpose

    Recombinant Human GAMT Protein (His Tag)

    Sequence

    Met 1-Gly236

    Characteristics

    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.

    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, 1 mM DTT, pH 8.0.

    Preservative

    Dithiothreitol (DTT)

    Precaution of Use

    This product contains Dithiothreitol (DTT): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    -20 °C

    Storage Comment

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

    Expiry Date

    6 months
  • Target

    GAMT (Guanidinoacetate N-Methyltransferase (GAMT))

    Alternative Name

    GAMT

    Background

    GAMT,Guanidinoacetate N-methyltransferase,PIG2,TP53I2,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.

    Molecular Weight

    Calculated MW: 29.5 kDa

    Observed MW: 27-32 kDa

    Gene ID

    2593

    UniProt

    Q14353
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