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GAMT antibody (N-Term)

The Rabbit Polyclonal anti-GAMT antibody has been validated for WB. It is suitable to detect GAMT in samples from Human.
Catalog No. ABIN631157

Quick Overview for GAMT antibody (N-Term) (ABIN631157)

Target

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

Reactivity

  • 25
  • 22
  • 8
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
Human

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

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  • 5
  • 5
  • 4
  • 1
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  • 1
Western Blotting (WB)
  • Binding Specificity

    • 9
    • 3
    • 2
    • 2
    • 2
    • 1
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    • 1
    • 1
    • 1
    N-Term

    Specificity

    GAMT antibody was raised against the N terminal of GAMT

    Purification

    Affinity purified

    Immunogen

    GAMT antibody was raised using the N terminal of GAMT corresponding to a region with amino acids MSAPSATPIFAPGENCSPAWGAAPAAYDAADTHLRILGKPVMERWETPYM
  • Application Notes

    WB: 0.25 µg/mL
    Optimal conditions should be determined by the investigator.

    Comment

    GAMT Blocking Peptide, (ABIN5613722), is also available for use as a blocking control in assays to test for specificity of this GAMT antibody

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Lyophilized powder. Add distilled water for a 1 mg/mL concentration of GAMT antibody in PBS

    Concentration

    Lot specific

    Buffer

    PBS

    Handling Advice

    Avoid repeated freeze/thaw cycles.
    Dilute only prior to immediate use.

    Storage

    4 °C/-20 °C

    Storage Comment

    Store at 2-8 °C for short periods. For longer periods of storage, store at -20 °C.
  • Target

    GAMT (Guanidinoacetate N-Methyltransferase (GAMT))

    Alternative Name

    GAMT

    Background

    GAMT is a methyltransferase that converts guanidoacetate to creatine, using S-adenosylmethionine as the methyl donor. Defects in its 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.

    Molecular Weight

    26 kDa (MW of target protein)
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