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GAMT anticorps (N-Term)

L’anticorps Lapin Polyclonal anti-GAMT a été validé pour WB. Il convient pour détecter GAMT dans des échantillons de Humain.
N° du produit ABIN631157

Aperçu rapide pour GAMT anticorps (N-Term) (ABIN631157)

Antigène

Voir toutes GAMT Anticorps
GAMT (Guanidinoacetate N-Methyltransferase (GAMT))

Reactivité

  • 25
  • 22
  • 8
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
Humain

Hôte

  • 39
  • 2
Lapin

Clonalité

  • 40
  • 1
Polyclonal

Conjugué

  • 22
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
Cet anticorp GAMT est non-conjugé

Application

  • 23
  • 12
  • 7
  • 5
  • 5
  • 4
  • 1
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Épitope

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

    Specificité

    GAMT antibody was raised against the N terminal of GAMT

    Purification

    Affinity purified

    Immunogène

    GAMT antibody was raised using the N terminal of GAMT corresponding to a region with amino acids MSAPSATPIFAPGENCSPAWGAAPAAYDAADTHLRILGKPVMERWETPYM
  • Indications d'application

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

    Commentaires

    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

    Conseil sur la manipulation

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

    Stock

    4 °C/-20 °C

    Stockage commentaire

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

    GAMT (Guanidinoacetate N-Methyltransferase (GAMT))

    Autre désignation

    GAMT

    Sujet

    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.

    Poids moléculaire

    26 kDa (MW of target protein)
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