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GAMT antibody

GAMT Reactivity: Human, Rat, Mouse IF Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN6570555
  • Target See all GAMT Antibodies
    GAMT (Guanidinoacetate N-Methyltransferase (GAMT))
    Reactivity
    • 25
    • 21
    • 7
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    Human, Rat, Mouse
    Host
    • 39
    • 2
    Rabbit
    Clonality
    • 40
    • 1
    Polyclonal
    Conjugate
    • 22
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    This GAMT antibody is un-conjugated
    Application
    • 23
    • 11
    • 7
    • 5
    • 5
    • 4
    • 2
    • 1
    • 1
    • 1
    • 1
    Immunofluorescence (IF)
    Purification
    Affinity purification
    Immunogen
    Recombinant fusion protein of human GAMT (NP_000147.1).
    Isotype
    IgG
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  • Application Notes
    IF 1:50-1:200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 mg/mL
    Buffer
    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    GAMT (Guanidinoacetate N-Methyltransferase (GAMT))
    Alternative Name
    GAMT (GAMT Products)
    Synonyms
    gamt antibody, zgc:123136 antibody, CCDS2 antibody, PIG2 antibody, TP53I2 antibody, AA571402 antibody, Spintz1 antibody, MGC75698 antibody, GAMT antibody, GMT antibody, guanidinoacetate N-methyltransferase L homeolog antibody, guanidinoacetate N-methyltransferase S homeolog antibody, guanidinoacetate N-methyltransferase antibody, guanidinoacetate methyltransferase antibody, gamt.L antibody, gamt.S antibody, gamt antibody, GAMT antibody, Gamt antibody
    Background
    The protein encoded by this gene is a methyltransferase that converts guanidoacetate to creatine, using S-adenosylmethionine as the methyl donor. Defects in this gene have been implicated in neurologic syndromes and muscular hypotonia, probably due to creatine deficiency and accumulation of guanidinoacetate in the brain of affected individuals. Two transcript variants encoding different isoforms have been described for this gene. Pseudogenes of this gene are found on chromosomes 2 and 13.
    Molecular Weight

    Observed_MW: 29kDa

    Calculated_MW: 26kDa/29kDa

    Gene ID
    2593
    UniProt
    Q14353
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