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Rabbit anti-Human GAMT Polyclonal Antibody

The antibody against GAMT was raised in rabbit using the Human GAMT as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, WB, IHC.

ADC-48493A

The antibody against GAMT was raised in rabbit using the Human GAMT as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, WB, IHC.

$600.00

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Specifications


Cat.No ADC-48493A ClonalityPolyclonal
Host SpeciesRabbitTarget NameGAMT
FormLiquidSpecies ReactivityHuman, Mouse, Rat, Zebrafish
IsotypeIgGStorage Buffer50% Glycerol, Avoid freeze / thaw cycles., PBS with 0.1% Sodium Azide
Purification MethodAntigen affinity purifiedConjugateNon-conjugated
ApplicationELISA, IHC, WBStorageUpon receipt

Immunogen Information


Immunogen DescriptionHuman GAMTTarget SpeciesHuman
Immunogen SequenceComplete sequences for the immunogen, target protein, and peptides are available upon request.Uniprot IDQ14353
Background Information
  • Uniprot Id

    Q14353

  • Target Species

    Human

  • Target Name

    GAMT

  • Target Full Name

    Guanidinoacetate N-methyltransferase

  • Target Function

    Converts guanidinoacetate to creatine, using S-adenosylmethionine as the methyl donor. Important in nervous system development.

  • Target Involvement

    Cerebral creatine deficiency syndrome 2 (CCDS2)

  • Target Protein Families

    Class I-like SAM-binding methyltransferase superfamily, RMT2 methyltransferase family

  • Target Tissue Specificity

    Expressed in liver.

  • Target Synonyms

    CCDS2; Epididymis secretory protein Li 20; GAMT; GAMT_HUMAN; Guanidinoacetate N methyltransferase; Guanidinoacetate N-methyltransferase; HEL-S-20; PIG2; TP53I2

  • Target 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.

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